User:Daniel Mietchen/Wikidata lists/Items with Disease Ontology IDs

{| class='wikitable sortable'

! Article

! instance of

! subclass of

! description

! Disease Ontology ID

! MeSH tree code

! Commons category

! image

|-

| 1,4-phenylenediamine allergic contact dermatitis

| class of disease

| allergic contact dermatitis

| allergic contact dermatitis that has allergic trigger 1,4-phenylenediamine

| [http://www.disease-ontology.org/?id=DOID:0040058 DOID:0040058]

|

|

|

|-

| 1-chloro-2,4-dinitrobenzene allergic contact dermatitis

| class of disease

| allergic contact dermatitis

| allergic contact dermatitis that has allergic trigger 1-chloro-2,4-dinitrobenzene

| [http://www.disease-ontology.org/?id=DOID:0040069 DOID:0040069]

|

|

|

|-

| 17q11 microdeletion syndrome

| class of disease

| chromosomal deletion syndrome
partial deletion of the long arm of chromosome 17

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060403 DOID:0060403]

|

|

|

|-

| 2,4-dinitrophenyl allergic contact dermatitis

| class of disease

| allergic contact dermatitis

| allergic contact dermatitis that has allergic trigger 2,4-dinitrophenyl group

| [http://www.disease-ontology.org/?id=DOID:0040079 DOID:0040079]

|

|

|

|-

| 2-hydroxyglutaric aciduria

| class of disease

| amino acid metabolic disorder
neurometabolic disease
cerebral organic aciduria
rare genetic epilepsy
amino acid or protein metabolism disease with epilepsy

| amino acid metabolic disorder that is an autosomal recessive neurometabolic disorder characterized by the significant elevation of urinary levels of hydroxyglutaric acid causing progressive brain damage

| [http://www.disease-ontology.org/?id=DOID:0050573 DOID:0050573]

|

|

|

|-

| 2q37 deletion syndrome

| class of disease

| chromosome abnormality
intellectual disability
chromosome 2q deletion
chromosomal deletion syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111704 DOID:0111704]

|

|

|

|-

| 3-methylcrotonyl-CoA carboxylase 1 deficiency

| class of disease

| 3-methylcrotonyl-CoA carboxylase deficiency

| 3-methylcrotonyl-CoA carboxylase deficiency that has material basis in homozygous or compound heterozygous mutation in the gene encoding the alpha subunit of 3-methylcrotonyl-CoA carboxylase on chromosome 3q27

| [http://www.disease-ontology.org/?id=DOID:0080579 DOID:0080579]

|

|

|

|-

| 3-methylcrotonyl-CoA carboxylase 2 deficiency

| class of disease

| 3-methylcrotonyl-CoA carboxylase deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080580 DOID:0080580]

|

|

|

|-

| 3-methylglutaconic aciduria 7A

| class of disease

|

| human disease

| [http://www.disease-ontology.org/?id=DOID:0081133 DOID:0081133]

|

|

|

|-

| 3-methylglutaconic aciduria type 1

| class of disease

| 3-methylglutaconic aciduria
genetic disease
autosomal recessive disease

| 3-methylglutaconic aciduria that has material basis in homozygous or compound heterozygous mutation in the AUH gene on chromosome 9q22

| [http://www.disease-ontology.org/?id=DOID:0110002 DOID:0110002]

|

|

|

|-

| 3-methylglutaconic aciduria type 4

| class of disease

| 3-methylglutaconic aciduria

| 3-methylglutaconic aciduria that is characterized by mild or intermittent urinary excretion of 3-methylglutaconic acid

| [http://www.disease-ontology.org/?id=DOID:0110006 DOID:0110006]

|

|

|

|-

| 3-methylglutaconic aciduria type IX

| class of disease

| 3-methylglutaconic aciduria
genetic disease
autosomal recessive disease

| 3-methylglutaconic aciduria that has material basis in homozygous mutation in the TIMM50 gene on chromosome 19q13

| [http://www.disease-ontology.org/?id=DOID:0070002 DOID:0070002]

|

|

|

|-

| 3MC syndrome 2

| class of disease

| 3MC syndrome

| 3MC syndrome that has material basis in homozygous mutation in the COLEC11 gene on chromosome 2p25

| [http://www.disease-ontology.org/?id=DOID:0060576 DOID:0060576]

|

|

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| 3MC syndrome 3

| class of disease

| 3MC syndrome

| 3MC congenital syndrome associated with the COLEC10 gene on chromosome 8q24

| [http://www.disease-ontology.org/?id=DOID:0060577 DOID:0060577]

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|

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| 4-tert-butylphenol allergic contact dermatitis

| class of disease

| allergic contact dermatitis

| allergic contact dermatitis that has allergic trigger 4-tert-butylphenol

| [http://www.disease-ontology.org/?id=DOID:0040068 DOID:0040068]

|

|

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| 4-vinylcyclohexene dioxide respiratory allergy

| class of disease

| respiratory allergy

| respiratory allergy that has allergic trigger 4-vinylcyclohexene dioxide

| [http://www.disease-ontology.org/?id=DOID:0040063 DOID:0040063]

|

|

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| 46 XX gonadal dysgenesis

| class of disease

| gonadal dysgenesis

| gonadal dysgenesis that is characterized by the lack of functional ovaries to induce puberty in an otherwise 46,XX female

| [http://www.disease-ontology.org/?id=DOID:14450 DOID:14450]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.706.316.064.249 C12.706.316.064.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.706.316.309.193 C12.706.316.309.193]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.875.253.064.249 C13.351.875.253.064.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.875.253.309.193 C13.351.875.253.309.193]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.316.064.249 C16.131.939.316.064.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.316.309.193 C16.131.939.316.309.193]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.119.064.249 C19.391.119.064.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.119.309.193 C19.391.119.309.193]

|

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| 46,XX sex reversal 1

| class of disease

| XX male syndrome
X-linked dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111761 DOID:0111761]

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| 46,XX sex reversal 2

| class of disease

| autosomal dominant disease
XX male syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111763 DOID:0111763]

|

|

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| 46,XX sex reversal 3

| class of disease

| XX male syndrome
X-linked dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111762 DOID:0111762]

|

|

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| 46,XX sex reversal 4

| class of disease

| autosomal dominant disease
XX male syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111764 DOID:0111764]

|

|

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| 46,XY sex reversal 1

| class of disease

| Y-linked disease
XY gonadal dysgenesis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111778 DOID:0111778]

|

|

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| 46,XY sex reversal 10

| class of disease

| hereditary lymphedema
familial hypertrophic cardiomyopathy
46,XY partial gonadal dysgenesis
XY gonadal dysgenesis
autosomal dominant disease
chromosomal deletion syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111775 DOID:0111775]

|

|

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| 46,XY sex reversal 2

| class of disease

| XY gonadal dysgenesis
X-linked disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111777 DOID:0111777]

|

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| 46,XY sex reversal 3

| class of disease

| autosomal dominant disease
XY gonadal dysgenesis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111772 DOID:0111772]

|

|

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| 46,XY sex reversal 4

| class of disease

| XY gonadal dysgenesis
chromosomal deletion syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111771 DOID:0111771]

|

|

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|-

| 46,XY sex reversal 5

| class of disease

| XY gonadal dysgenesis
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111776 DOID:0111776]

|

|

|

|-

| 46,XY sex reversal 6

| class of disease

| XY gonadal dysgenesis
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111769 DOID:0111769]

|

|

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| 46,XY sex reversal 7

| class of disease

| autosomal recessive disease
XY gonadal dysgenesis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111774 DOID:0111774]

|

|

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| 46,XY sex reversal 8

| class of disease

| autosomal recessive disease
XY gonadal dysgenesis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111773 DOID:0111773]

|

|

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| 46,XY sex reversal 9

| class of disease

| autosomal dominant disease
XY gonadal dysgenesis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111770 DOID:0111770]

|

|

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|-

| ABCD syndrome

| class of disease

| autosomal recessive disease
Waardenburg-Shah syndrome
syndrome

| Autosomal recessive disease that is characterized by albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness and has material basis in a mutation in the endothelin B receptor gene (EDNRB)

| [http://www.disease-ontology.org/?id=DOID:0050600 DOID:0050600]

|

|

|

|-

| ABri amyloidosis

| class of disease

| cerebral amyloid angiopathy
ITM2B amyloidosis
genetic disease
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070029 DOID:0070029]

|

|

|

|-

| ACTH-independent macronodular adrenal hyperplasia 1

| class of disease

| Cushing syndrome due to macronodular adrenal hyperplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111623 DOID:0111623]

|

|

|

|-

| ACTH-independent macronodular adrenal hyperplasia 2

| class of disease

| Cushing syndrome due to macronodular adrenal hyperplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111624 DOID:0111624]

|

|

|

|-

| AMED syndrome

| class of disease

| syndrome
autosomal recessive disease
digenic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080952 DOID:0080952]

|

|

|

|-

| APP-related cerebral amyloid angiopathy

| class of disease

| cerebral amyloid angiopathy
autosomal dominant disease

| A cerebral amyloid angiopathy that has material basis in an autosomal dominant mutation of APP on chromosome 21q21.3.

| [http://www.disease-ontology.org/?id=DOID:0070028 DOID:0070028]

|

|

|

|-

| Aagenaes syndrome

| class of disease

| syndrome
primary lymphedema with associated anomalies
genetic vascular anomaly
rare genetic hepatic disease
syndromic lymphedema
rare genetic immune disease
disease

| syndrome that is characterized by congenital hypoplasia of lymph vessels, which causes lymphedema of the legs and recurrent cholestasis in infancy, and slow progress to hepatic cirrhosis and giant cell hepatitis with fibrosis of the portal tracts

| [http://www.disease-ontology.org/?id=DOID:6691 DOID:6691]

|

| Aagenaes syndrome

| File:Primary intestinal lymphangiectasia (Waldmann's disease) - legs.jpg

|-

| Achard syndrome

| class of disease

| syndrome
genetic disease

| syndrome that involves arachnodactyly, receding lower jaw, and joint laxity limited to the hands and feet

| [http://www.disease-ontology.org/?id=DOID:6686 DOID:6686]

|

|

|

|-

| Achenbach syndrome

| class of disease

| skin disease

| skin condition characterized by spontaneous focal hemorrhage into the palm or the volar surface of a finger

| [http://www.disease-ontology.org/?id=DOID:6687 DOID:6687]

|

| Paroxysmal hand hematoma

|

|-

| Acinetobacter infectious disease

| class of disease

| gram-negative bacterial infection
opportunistic bacterial infectious disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3091 DOID:3091]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.400.560.022 C01.150.252.400.560.022]

|

|

|-

| Adie syndrome

| class of disease

| syndrome
abnormal pupillary function
disease

| neurological disorder characterized by a tonically dilated pupil

| [http://www.disease-ontology.org/?id=DOID:11549 DOID:11549]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.177.045 C10.177.045]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.562.700.250 C10.292.562.700.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.590.436.200 C11.590.436.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.710.800.180 C11.710.800.180]

| Adie syndrome

| File:Adies.png

|-

| African histoplasmosis

| class of disease

| histoplasmosis
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11315 DOID:11315]

|

|

|

|-

| African iron overload

| class of disease

| iron overload
HFE hereditary haemochromatosis

| hemochromatosis characterized by a predisposition to iron loading that is exacerbated by excessive intake of dietary iron, commonly related to consumption of tradition beer brewed in non-galvanized steel drums

| [http://www.disease-ontology.org/?id=DOID:0111033 DOID:0111033]

|

|

|

|-

| African tick-bite fever

| class of disease

| spotted fever
disease

| spotted fever that has material basis in Rickettsia africae, which is transmitted by ticks

| [http://www.disease-ontology.org/?id=DOID:0050035 DOID:0050035]

|

| African tick bite fever

| File:African tick bite fever - leg lesion.jpg

|-

| Alkhurma hemorrhagic fever

| class of disease

| Kyasanur forest disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050308 DOID:0050308]

|

|

|

|-

| Alkuraya-Kučinskas syndrome

| class of disease

| cerebral malformation
autosomal recessive disease
syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111555 DOID:0111555]

|

|

|

|-

| Alpha-thalassemia mental retardation syndrome

| class of disease
rare disease
developmental defect during embryogenesis
designated intractable/rare disease

| alpha thalassemia
alpha-thalassemia-related diseases
X-linked dominant disease
X-linked intellectual disability
ATR-X-related syndrome
syndrome with 46,XY disorder of sex development
syndrome with disorder of sex development of gynecological interest

| alpha thalassemia that has material basis in mutation in the ATRX gene on Xq21

| [http://www.disease-ontology.org/?id=DOID:0110030 DOID:0110030]

|

| Alpha-thalassemia mental retardation syndrome

| File:Atr-x.jpg

|-

| Alteración del estado mental

| class of disease

| schizophrenia
disease

|

| [http://www.disease-ontology.org/?id=DOID:1229 DOID:1229]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.700.750.600 F03.700.750.600]

|

|

|-

| Alwadei syndrome

| class of disease

| autosomal recessive non-syndromic intellectual disability
neurodevelopmental disorder

| autosomal recessive non-syndromic intellectual disability that has material basis in an autosomal recessive mutation of the RUSC2 gene on chromosome 9p13

| [http://www.disease-ontology.org/?id=DOID:0080239 DOID:0080239]

|

|

|

|-

| Alzheimer disease 10

| class of disease

| Alzheimer's disease
early-onset autosomal dominant Alzheimer disease

| Alzheimer's disease that is characterized by an associated with variation in the region 7q36

| [http://www.disease-ontology.org/?id=DOID:0110043 DOID:0110043]

|

|

|

|-

| Alzheimer disease 11

| class of disease

| Alzheimer's disease
early-onset autosomal dominant Alzheimer disease

| An Alzheimer's disease that is characterized by an associated with variation in the region 9p22.1.

| [http://www.disease-ontology.org/?id=DOID:0110044 DOID:0110044]

|

|

|

|-

| Alzheimer disease 12

| class of disease

| Alzheimer's disease
early-onset autosomal dominant Alzheimer disease

| Alzheimer's disease that is characterized by an associated with variation in the region 8p12-q22

| [http://www.disease-ontology.org/?id=DOID:0110045 DOID:0110045]

|

|

|

|-

| Alzheimer disease 13

| class of disease

| Alzheimer's disease
early-onset autosomal dominant Alzheimer disease

| Alzheimer's disease that is characterized by an associated with variation in the region 1q21

| [http://www.disease-ontology.org/?id=DOID:0110046 DOID:0110046]

|

|

|

|-

| Alzheimer disease 14

| class of disease

| Alzheimer's disease
early-onset autosomal dominant Alzheimer disease

| Alzheimer's disease that is characterized by an associated with variation in the region 1q25

| [http://www.disease-ontology.org/?id=DOID:0110047 DOID:0110047]

|

|

|

|-

| Alzheimer disease 15

| class of disease

| Alzheimer's disease
early-onset autosomal dominant Alzheimer disease

| Alzheimer's disease that is characterized by an associated with variations in the region 3q22-q24

| [http://www.disease-ontology.org/?id=DOID:0110048 DOID:0110048]

|

|

|

|-

| Alzheimer disease 16

| class of disease

| Alzheimer's disease

| An Alzheimer's disease that is characterized by an associated with a risk allele in in the PCDH11X gene on chromosome Xq21.3.

| [http://www.disease-ontology.org/?id=DOID:0110036 DOID:0110036]

|

|

|

|-

| Alzheimer disease 17

| class of disease

| Alzheimer's disease

| Alzheimer's disease that is characterized by an associated with mutations in the gene TREM2

| [http://www.disease-ontology.org/?id=DOID:0110049 DOID:0110049]

|

|

|

|-

| Alzheimer disease 18

| class of disease

| Alzheimer's disease

| Alzheimer's disease that has material basis in a mutation in the ADAM10 gene on chromosome 15q21

| [http://www.disease-ontology.org/?id=DOID:0110050 DOID:0110050]

|

|

|

|-

| Alzheimer disease 19

| class of disease

| Alzheimer's disease

| Alzheimer's disease that is characterized by associated variants of the gene PLD3

| [http://www.disease-ontology.org/?id=DOID:0110051 DOID:0110051]

|

|

|

|-

| Alzheimer disease 5

| class of disease

| Alzheimer's disease
early-onset autosomal dominant Alzheimer disease
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110037 DOID:0110037]

|

|

|

|-

| Alzheimer disease 6

| class of disease

| Alzheimer's disease
early-onset autosomal dominant Alzheimer disease

| Alzheimer's disease that is characterized by an associated with variation in the region 10q24

| [http://www.disease-ontology.org/?id=DOID:0110038 DOID:0110038]

|

|

|

|-

| Alzheimer disease 7

| class of disease

| Alzheimer's disease
early-onset autosomal dominant Alzheimer disease

| Alzheimer's disease that is characterized by an associated with variation in the region 10p13

| [http://www.disease-ontology.org/?id=DOID:0110039 DOID:0110039]

|

|

|

|-

| Alzheimer disease 8

| class of disease

| Alzheimer's disease
early-onset autosomal dominant Alzheimer disease

| An Alzheimer's disease that is characterized by an associated with variation in the region 20p12.2-q11.21.

| [http://www.disease-ontology.org/?id=DOID:0110041 DOID:0110041]

|

|

|

|-

| Alzheimer's disease 1

| class of disease

| autosomal dominant disease
Alzheimer's disease

| Alzheimer's disease that has material basis in mutation in the gene encoding the amyloid precursor protein on chromosome 21q

| [http://www.disease-ontology.org/?id=DOID:0080348 DOID:0080348]

|

|

|

|-

| Alzheimer's disease 9

| class of disease

| autosomal dominant disease
Alzheimer's disease
early-onset autosomal dominant Alzheimer disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111364 DOID:0111364]

|

|

|

|-

| Ambras type hypertrichosis universalis congenita

| class of disease

| hypertrichosis
hypertrichosis lanuginosa congenita

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111060 DOID:0111060]

|

|

|

|-

| American histoplasmosis

| class of disease

| histoplasmosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1759 DOID:1759]

|

|

|

|-

| Angelucci's syndrome

| class of disease

| allergic conjunctivitis
acute conjunctivitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11203 DOID:11203]

|

|

|

|-

| Arakawa's syndrome I

| class of disease

| syndrome
disorder of folate metabolism and transport
constitutional megaloblastic anemia due to folate metabolism disorder
vitamin metabolic disorder
autosomal recessive disease

| genetic disorder

| [http://www.disease-ontology.org/?id=DOID:0111679 DOID:0111679]

|

|

|

|-

| Arenaviridae infectious disease

| class of disease

| (-)ssRNA virus infectious disease
viral infectious disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3944 DOID:3944]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C02.782.082 C02.782.082]

|

|

|-

| Argyll Robertson pupil

| class of disease

| abnormal pupillary function
disease

| symptom of human disease

| [http://www.disease-ontology.org/?id=DOID:14523 DOID:14523]

|

| Argyll Robertson pupil

| File:Argyll Robertson pupil light reflex vs accommodation reflex.jpg

|-

| Askin's tumor

| class of disease

| Ewing sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050608 DOID:0050608]

|

|

|

|-

| Astrakhan spotted fever

| class of disease

| spotted fever

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050041 DOID:0050041]

|

|

|

|-

| Atlantic cod allergy

| class of disease

| fish allergy

| fish allergy triggered by Gadus morhua

| [http://www.disease-ontology.org/?id=DOID:0060514 DOID:0060514]

|

|

|

|-

| Atlantic salmon allergy

| class of disease

| fish allergy

| fish allergy triggered by Salmo salar

| [http://www.disease-ontology.org/?id=DOID:0060515 DOID:0060515]

|

|

|

|-

| Axenfeld-Rieger syndrome

| class of disease

| autosomal dominant disease
eye disease

| autosomal dominant disease characterized by abnormalities of the front part of the eye, the anterior segment

| [http://www.disease-ontology.org/?id=DOID:14686 DOID:14686]

|

| Axenfeld syndrome

|

|-

| Axenfeld-Rieger syndrome type 2

| class of disease

| Axenfeld-Rieger syndrome
chromosomal deletion syndrome

| Axenfeld-Rieger syndrome that has material basis in deletions in the region 13q14

| [http://www.disease-ontology.org/?id=DOID:0110121 DOID:0110121]

|

|

|

|-

| B cell and dendritic cell deficiency

| class of disease

| combined immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111964 DOID:0111964]

|

|

|

|-

| B cell deficiency

| class of disease

| primary immunodeficiency disease

| primary immunnodeficiency disease that is caused by a lack of infection-fighting antibody producing B cells (immunoglobulins) or B cells that are not functioning properly

| [http://www.disease-ontology.org/?id=DOID:2115 DOID:2115]

|

|

|

|-

| B cell linker protein deficiency

| class of disease

| agammaglobulinemia
autosomal recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060027 DOID:0060027]

|

|

|

|-

| B-cell acute lymphoblastic leukemia

| class of disease

| acute lymphocytic leukemia
lymphoma
B-cell leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080638 DOID:0080638]

|

|

|

|-

| B-cell adult acute lymphocytic leukemia

| class of disease

| adult acute lymphocytic leukemia
B-cell childhood acute lymphoblastic leukemia
lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060592 DOID:0060592]

|

|

|

|-

| B-cell childhood acute lymphoblastic leukemia

| class of disease

| childhood acute lymphocytic leukemia
B-cell acute lymphoblastic leukemia
lymphoma

| childhood acute lymphoblastic leukemia that has material basis in B-cells

| [http://www.disease-ontology.org/?id=DOID:0080146 DOID:0080146]

|

|

|

|-

| B-cell lymphoma

| class of disease

| non-Hodgkin lymphoma
leukocyte disease
immune disorder

| non-Hodgkin lymphoma that has material basis in B cells

| [http://www.disease-ontology.org/?id=DOID:707 DOID:707]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386.480.150 C04.557.386.480.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.569.480.150 C15.604.515.569.480.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.761.480.150 C20.683.515.761.480.150]

| B-cell lymphomas

| File:Lymphoma, B-cell type, small cell, well-differentaited Case 173 (5601360422).jpg

|-

| B-cell prolymphocytic leukemia

| class of disease

| prolymphocytic leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0081041 DOID:0081041]

|

|

|

|-

| B-lymphoblastic leukemia/lymphoma KMT2A rearranged

| class of disease

| precursor B lymphoblastic lymphoma/leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080644 DOID:0080644]

|

|

|

|-

| B-lymphoblastic leukemia/lymphoma with BCR-ABL1

| class of disease

| precursor B lymphoblastic lymphoma/leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080643 DOID:0080643]

|

|

|

|-

| B-lymphoblastic leukemia/lymphoma with ETV6-RUNX1

| class of disease

| precursor B lymphoblastic lymphoma/leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080645 DOID:0080645]

|

|

|

|-

| B-lymphoblastic leukemia/lymphoma with IL3-IGH

| class of disease

| precursor B lymphoblastic lymphoma/leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080648 DOID:0080648]

|

|

|

|-

| B-lymphoblastic leukemia/lymphoma with TCF3-PBX1

| class of disease

| precursor B lymphoblastic lymphoma/leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080649 DOID:0080649]

|

|

|

|-

| B-lymphoblastic leukemia/lymphoma with hyperdiploidy

| class of disease

| precursor B lymphoblastic lymphoma/leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080646 DOID:0080646]

|

|

|

|-

| B-lymphoblastic leukemia/lymphoma with hypodiploidy

| class of disease

| precursor B lymphoblastic lymphoma/leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080647 DOID:0080647]

|

|

|

|-

| B-lymphoblastic leukemia/lymphoma with iAMP21

| class of disease

| precursor B lymphoblastic lymphoma/leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080651 DOID:0080651]

|

|

|

|-

| B-lymphoblastic leukemia/lymphoma, BCR-ABL1–like

| class of disease

| precursor B lymphoblastic lymphoma/leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080650 DOID:0080650]

|

|

|

|-

| BIDS syndrome

| class of disease

| trichothiodystrophy syndromes
autosomal recessive disease
nonphotosensitive trichothiodystrophy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050528 DOID:0050528]

|

|

|

|-

| Balkan hemorrhagic fever

| class of disease

| hemorrhagic fever with renal syndrome

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050522 DOID:0050522]

|

|

|

|-

| Balkan nephropathy

| class of disease

| interstitial nephritis
Alport syndrome

| interstitial nephritis endemic to the regions along the Danube river, in the modern countries of Croatia, Bosnia and Herzegovina, Serbia, Romania and Bulgaria

| [http://www.disease-ontology.org/?id=DOID:3052 DOID:3052]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.777.419.570.643.150 C12.200.777.419.570.643.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.968.419.570.643.150 C12.050.351.968.419.570.643.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.950.419.570.643.150 C12.950.419.570.643.150]

|

|

|-

| Balo concentric sclerosis

| class of disease

| demyelinating disease
neurodegeneration
multiple sclerosis
disease

| demyelinating disease characterized by the fact that the demyelinated tissues form concentric layers

| [http://www.disease-ontology.org/?id=DOID:0060215 DOID:0060215]

|

| Balo concentric sclerosis

|

|-

| Bardet-Biedl syndrome 1

| class of disease

| Bardet-Biedl syndrome

| Bardet-Biedl syndrome that has material basis in homozygous mutation in the BBS1 gene on chromosome 11q13

| [http://www.disease-ontology.org/?id=DOID:0110123 DOID:0110123]

|

|

|

|-

| Barrett's adenocarcinoma

| class of disease

| esophagus adenocarcinoma

| adenocarcinoma arising in Barrett's mucosa

| [http://www.disease-ontology.org/?id=DOID:7941 DOID:7941]

|

|

|

|-

| Barrett's esophagus

| class of disease

| esophageal disease
disease

| esophagus condition

| [http://www.disease-ontology.org/?id=DOID:9206 DOID:9206]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.834.154 C04.834.154]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.117.102 C06.405.117.102]

| Barrett's esophagus

| File:Barretts esophagus.jpg

|-

| Bartholin's duct cyst

| class of disease

| Bartholin's gland disease
disease

| cyst in a blocked Bartholin's gland

| [http://www.disease-ontology.org/?id=DOID:851 DOID:851]

|

| Bartholin's cyst

| File:Barthonlincyst2011.png

|-

| Bartholin's gland adenocarcinoma

| class of disease

| Bartholin's gland carcinoma
adenocarcinoma
vulva adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6316 DOID:6316]

|

|

|

|-

| Bartholin's gland adenoid cystic carcinoma

| class of disease

| Bartholin's gland carcinoma
Bartholin's gland adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4879 DOID:4879]

|

|

|

|-

| Bartholin's gland adenoma

| class of disease

| Bartholin's gland benign neoplasm
benign epithelial neoplasm
benign neoplasms by histologic type
Bartholin's gland disease
adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5382 DOID:5382]

|

|

|

|-

| Bartholin's gland adenomyoma

| class of disease

| Bartholin's gland benign neoplasm
adenomyoma
Bartholin's gland carcinoma
Bartholin's gland disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6518 DOID:6518]

|

|

|

|-

| Bartholin's gland adenosquamous carcinoma

| class of disease

| adenosquamous carcinoma
Bartholin's gland squamous cell carcinoma
Bartholin's gland carcinoma

| Bartholin's gland carcinoma that derives from squamous cells and gland-like cells

| [http://www.disease-ontology.org/?id=DOID:5630 DOID:5630]

|

|

|

|-

| Bartholin's gland benign neoplasm

| class of disease

| vestibular gland benign neoplasm
bartholin gland neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2068 DOID:2068]

|

|

|

|-

| Bartholin's gland cancer

| class of disease

| vulvar cancer
Bartholin's gland disease

| vulva cancer that is located in Bartholin's gland

| [http://www.disease-ontology.org/?id=DOID:60003 DOID:60003]

|

|

|

|-

| Bartholin's gland carcinoma

| class of disease

| vulva carcinoma
Bartholin's gland benign neoplasm
Bartholin's gland cancer
disease

| vulva carcinoma that has material basis in abnormally proliferating cells derives from epithelial cells and is located in Bartholin's gland

| [http://www.disease-ontology.org/?id=DOID:3999 DOID:3999]

|

|

|

|-

| Bartholin's gland disease

| class of disease

| female reproductive system disease

| Disease that is located in Bartholin's gland

| [http://www.disease-ontology.org/?id=DOID:60002 DOID:60002]

|

|

|

|-

| Bartholin's gland small cell carcinoma

| class of disease

| Bartholin's gland carcinoma
female reproductive organ cancer
small cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7140 DOID:7140]

|

|

|

|-

| Bartholin's gland squamous cell carcinoma

| class of disease

| Bartholin's gland carcinoma
squamous cell carcinoma
vulva squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6961 DOID:6961]

|

|

|

|-

| Bartholin's gland transitional cell carcinoma

| class of disease

| Bartholin's gland carcinoma
transitional cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3998 DOID:3998]

|

|

|

|-

| Bartter disease type 1

| class of disease

| Bartter disease

| A Bartter disease that has material basis in homozygous or compound heterozygous mutation in the sodium-potassium-chloride cotransporter-2 gene (SLC12A1) on chromosome 15q21.

| [http://www.disease-ontology.org/?id=DOID:0110142 DOID:0110142]

|

|

|

|-

| Bartter disease type 2

| class of disease

| Bartter disease

| A Bartter disease that has material basis in homozygous or compound heterozygous mutation in the potassium channel ROMK gene (KCNJ1) on chromosome 11q24.

| [http://www.disease-ontology.org/?id=DOID:0110143 DOID:0110143]

|

|

|

|-

| Bartter disease type 4b

| class of disease

| Bartter disease
infantile Bartter syndrome with sensorineural deafness

| Bartter disease that has material basis in simultaneous mutation in both the CLCNKA and CLCNKB genes

| [http://www.disease-ontology.org/?id=DOID:0110146 DOID:0110146]

|

|

|

|-

| Bartter disease type 5

| class of disease

| Bartter disease

| Bartter disease that has material basis in mutation in the MAGED2 gene on chromosome Xp11

| [http://www.disease-ontology.org/?id=DOID:0110147 DOID:0110147]

|

|

|

|-

| Basilicata-Akhtar syndrome

| class of disease

| X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111838 DOID:0111838]

|

|

|

|-

| Beckwith-Wiedemann syndrome

| class of disease

| syndrome
overgrowth syndrome
disease

| syndrome characterized by overgrowth (macrosomia), an increased risk of childhood cancer and congenital malformations

| [http://www.disease-ontology.org/?id=DOID:5572 DOID:5572]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.077.133 C16.131.077.133]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.260.080 C16.131.260.080]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.180.080 C16.320.180.080]

|

|

|-

| Beemer-Langer syndrome

| class of disease

| short rib – polydactyly syndrome
syndrome

| syndrome that results in multiple congenital anomalies, including hydrops fetalis, facial and visceral abnormalities, short ribs, and short limbs without polydactyly

| [http://www.disease-ontology.org/?id=DOID:9249 DOID:9249]

|

|

|

|-

| Behcet's syndrome arthropathy

| class of disease

| arthropathy
Behçet's disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1670 DOID:1670]

|

|

|

|-

| Bell's palsy

| class of disease
symptom or sign

| facial paralysis
palsy
disease

| facial paralysis resulting from dysfunction in the cranial nerve VII (facial nerve)

| [http://www.disease-ontology.org/?id=DOID:12506 DOID:12506]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.256.466.087 C01.925.256.466.087]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.094 C07.465.094]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.299.250 C07.465.299.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.319.250 C10.292.319.250]

| Bell's palsy

| File:Bells palsy diagram.svg

|-

| Bellini duct carcinoma

| class of disease

| renal carcinoma
renal cell carcinoma

| disease

| [http://www.disease-ontology.org/?id=DOID:4464 DOID:4464]

|

| Collecting duct carcinoma

|

|-

| Bernard-Soulier syndrome

| class of disease

| Giant platelet disorder
inherited blood coagulation disease
blood coagulation disease
autosomal recessive disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2217 DOID:2217]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100.100.080 C15.378.100.100.080]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.140.120 C15.378.140.120]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463.080 C15.378.463.080]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.099.080 C16.320.099.080]

|

|

|-

| Blessig's cysts

| class of disease

| peripheral retinal degeneration
retinoschisis and retinal cysts

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12164 DOID:12164]

|

|

|

|-

| Bordetella parapertussis whooping cough

| class of disease

| pertussis

| A pertussis that is a milder disease caused by the bacterium Bordetella parapertussis. The disease has symptom coughing, has symptom sneezing, or has symptom runny nose .

| [http://www.disease-ontology.org/?id=DOID:11750 DOID:11750]

|

|

|

|-

| Borst-Jadassohn intraepidermal carcinoma

| class of disease

| skin carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7039 DOID:7039]

|

|

|

|-

| Bowman's membrane folds or rupture

| class of disease

| corneal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11552 DOID:11552]

|

|

|

|-

| Brainstem glioma

| class of disease

| brain stem cancer
glioma
brain glioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4202 DOID:4202]

|

| Brainstem gliomas

|

|-

| Brown's tendon sheath syndrome

| class of disease

| mechanical strabismus
genetic disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10235 DOID:10235]

|

|

|

|-

| Brown-Vialetto-Van Laere syndrome

| class of disease

| autosomal dominant disease
infantile progressive bulbar palsy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050694 DOID:0050694]

|

|

|

|-

| Brown-Vialetto-Van Laere syndrome 1

| class of disease

| autosomal recessive disease
Brown-Vialetto-Van Laere syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080785 DOID:0080785]

|

|

|

|-

| Brugada syndrome 1

| class of disease

| Brugada syndrome
autosomal dominant disease

| Brugada syndrome that has material basis in heterozygous mutation in the SCN5A gene on chromosome 3p22

| [http://www.disease-ontology.org/?id=DOID:0110218 DOID:0110218]

|

|

|

|-

| Brugada syndrome 7

| class of disease

| Brugada syndrome
autosomal dominant disease

| Brugada syndrome that has material basis in heterozygous mutation in the SCN3B gene on chromosome 11q24

| [http://www.disease-ontology.org/?id=DOID:0110224 DOID:0110224]

|

|

|

|-

| Buruli ulcer disease

| class of disease

| primary bacterial infectious disease
mycobacterium infectious disease
neglected tropical disease
disease

| tropical disease

| [http://www.disease-ontology.org/?id=DOID:0050456 DOID:0050456]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.410.040.552.475.247 C01.150.252.410.040.552.475.247]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.893.295 C17.800.893.295]

| Buruli ulcer

| File:Buruli ulcer left ankle EID.jpg

|-

| Buschke–Ollendorff syndrome

| class of disease

| osteopetrosis
syndrome
autosomal dominant disease

| medical condition

| [http://www.disease-ontology.org/?id=DOID:0111536 DOID:0111536]

|

| Buschke–Ollendorff syndrome

|

|-

| C-P angle neurinoma

| class of disease

| neurilemmoma
cerebellopontine angle tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3199 DOID:3199]

|

|

|

|-

| CADASIL 1

| class of disease

| CADASIL
autosomal dominant disease

| CADASIL characterized by migraine, strokes, and white matter lesions that has material basis in heterozygous mutation in the NOTCH3 gene on chromosome 19p13

| [http://www.disease-ontology.org/?id=DOID:0111035 DOID:0111035]

|

|

|

|-

| CAKUT1

| class of disease

| CAKUT

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080206 DOID:0080206]

|

|

|

|-

| CD3delta deficiency

| class of disease

| severe combined immunodeficiency
T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta
autosomal recessive disease
primary immunodeficiency disease

| A severe combined immunodeficiency that is characterized by the absence of T cells but normal numbers of B cells. CD3D is essential for T cell development.

| [http://www.disease-ontology.org/?id=DOID:0060016 DOID:0060016]

|

|

|

|-

| CD3epsilon deficiency

| class of disease

| severe combined immunodeficiency
autosomal recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060017 DOID:0060017]

|

|

|

|-

| CD40 ligand deficiency

| class of disease

| combined immunodeficiency
X-linked hyper IgM syndrome
X-linked recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060022 DOID:0060022]

|

|

|

|-

| CLOVES syndrome

| class of disease

| overgrowth syndrome
subcutaneous tissue disease
rare genetic vascular tumor
nevus
complex vascular malformation with associated anomalies
genetic skin vascular disorder
rare genetic subcutaneous tissue disorder
syndrome
PIK3CA-related overgrowth spectrum

| CLOVE syndrome is characterized by Congenital Lipomatous Overgrowth, progressive, complex and mixed truncal Vascular malformations, and Epidermal nevi

| [http://www.disease-ontology.org/?id=DOID:0080351 DOID:0080351]

|

|

|

|-

| COACH Syndrome

| class of disease

| syndrome
Joubert syndrome
Joubert syndrome and related disorders
autosomal recessive disease

| a rare autosomal recessive disorder characterised by Cerebellar vermis hypoplasia, Oligophrenia (developmental delay/mental retardation), Ataxia, Coloboma, and Hepatic fibrosis.

| [http://www.disease-ontology.org/?id=DOID:0111589 DOID:0111589]

|

|

|

|-

| CREST syndrome

| class of disease

| syndrome
limited scleroderma
disease

| syndrome characterized by calcinosis, Raynaud's phenomeno, esophageal dysmotility, sclerodactyly and telangiectasia

| [http://www.disease-ontology.org/?id=DOID:0060218 DOID:0060218]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.117.119.500.204 C06.405.117.119.500.204]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.617.812.500 C14.907.617.812.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.823.225 C14.907.823.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.799.801.500 C17.300.799.801.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.784.801.500 C17.800.784.801.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.174.130.204 C18.452.174.130.204]

| CREST syndrome

|

|-

| Caplan's syndrome

| class of disease

| pneumoconiosis
rheumatoid lung disease
disease

| pneumoconiosis that results in humans that also have rheumatoid arthritis

| [http://www.disease-ontology.org/?id=DOID:10326 DOID:10326]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.550.114.154.219 C05.550.114.154.219]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.799.114.219 C05.799.114.219]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.483.581.300 C08.381.483.581.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.520.702.300 C08.381.520.702.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.775.099.219 C17.300.775.099.219]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C24.800.340 C24.800.340]

|

|

|-

| Carrion's disease

| class of disease

| bartonellosis
disease

| infectious disease produced by Bartonella bacilliformis infection

| [http://www.disease-ontology.org/?id=DOID:0050398 DOID:0050398]

|

| Carrion's disease

| File:Verruga peruana.jpg

|-

| Cervicocranial syndrome

| class of disease

| syndrome
neurological disorder

| syndrome that involves occipital head aches, nystagmus on head movement, tinnitus, spasms, blurred vision, corneal hyperaesthesia, and corneal ulcers

| [http://www.disease-ontology.org/?id=DOID:6692 DOID:6692]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.900.596 C05.116.900.596]

|

|

|-

| Chandler syndrome

| class of disease

| corneal dystrophy
iridocorneal endothelial syndrome

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11554 DOID:11554]

|

|

|

|-

| Charcot-Marie-Tooth disease axonal type 2H

| class of disease

| Charcot-Marie-Tooth disease type 2
autosomal recessive axonal hereditary motor and sensory neuropathy
autosomal recessive disease

| Charcot-Marie-Tooth disease type 2 that has material basis in variation in the region 8q13-q23

| [http://www.disease-ontology.org/?id=DOID:0110166 DOID:0110166]

|

|

|

|-

| Charcot-Marie-Tooth disease dominant intermediate A

| class of disease

| Charcot-Marie-Tooth disease intermediate type
autosomal dominant intermediate Charcot-Marie-Tooth disease
autosomal dominant disease

| A Charcot-Marie-Tooth disease intermediate type that has material basis in variation in the region 10q24.1-q25.1.

| [http://www.disease-ontology.org/?id=DOID:0110202 DOID:0110202]

|

|

|

|-

| Charcot-Marie-Tooth disease dominant intermediate G

| class of disease

| Charcot-Marie-Tooth disease intermediate type

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080294 DOID:0080294]

|

|

|

|-

| Charcot-Marie-Tooth disease intermediate type

| class of disease

| Charcot–Marie–Tooth disease

| Charcot-Marie-Tooth disease characterized by motor conduction velocities above and below 38 m/s

| [http://www.disease-ontology.org/?id=DOID:0050543 DOID:0050543]

|

|

|

|-

| Charcot-Marie-Tooth disease type 1

| class of disease

| Charcot–Marie–Tooth disease
autosomal dominant hereditary demyelinating motor and sensory neuropathy

| Charcot-Marie-Tooth disease characterized by demyelination of the peripheral nerve axons

| [http://www.disease-ontology.org/?id=DOID:0050538 DOID:0050538]

|

|

|

|-

| Charcot-Marie-Tooth disease type 1G

| class of disease

| Charcot-Marie-Tooth disease type 1
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111560 DOID:0111560]

|

|

|

|-

| Charcot-Marie-Tooth disease type 2A2B

| class of disease

| Charcot-Marie-Tooth disease type 2
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111557 DOID:0111557]

|

|

|

|-

| Charcot-Marie-Tooth disease type 2DD

| class of disease

| autosomal dominant disease
Charcot-Marie-Tooth disease type 2

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111558 DOID:0111558]

|

|

|

|-

| Charcot-Marie-Tooth disease type 2EE

| class of disease

| Charcot-Marie-Tooth disease type 2
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111559 DOID:0111559]

|

|

|

|-

| Charcot-Marie-Tooth disease type 3

| class of disease

| Charcot–Marie–Tooth disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050540 DOID:0050540]

|

|

|

|-

| Charcot-Marie-Tooth disease type 4

| class of disease

| Charcot–Marie–Tooth disease
autosomal recessive hereditary demyelinating motor and sensory neuropathy

| Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has material basis in autosomal recessive inheritance

| [http://www.disease-ontology.org/?id=DOID:0050541 DOID:0050541]

|

|

|

|-

| Charcot-Marie-Tooth disease type 7

| class of disease

| Charcot–Marie–Tooth disease

| Charcot-Marie-Tooth disease that is characterized by optic atrophy followed by retinitis pigmentosa

| [http://www.disease-ontology.org/?id=DOID:0080069 DOID:0080069]

|

|

|

|-

| Charcot-Marie-tooth disease type 5

| class of disease

| Charcot–Marie–Tooth disease
hereditary spastic paraplegia
autosomal dominant disease

| Charcot-Marie-Tooth disease that is characterized by pyramidal features including extensor plantar responses, mild increase in tone, and preserved or increased reflexes but no spastic gait

| [http://www.disease-ontology.org/?id=DOID:0080067 DOID:0080067]

|

|

|

|-

| Chediak-Higashi syndrome

| class of disease

| autosomal recessive disease
nervous system heredodegenerative disease
eye degenerative disease
syndrome
disease

| rare autosomal recessive disorder related to lysossomal function and the CHS1 gene

| [http://www.disease-ontology.org/?id=DOID:2935 DOID:2935]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.553.774.257 C15.378.553.774.257]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.673.774.257 C20.673.774.257]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.270.040.772 C11.270.040.772]

| Chediak-Higashi syndrome

|

|-

| Clostridioides difficile colitis

| class of disease

| colitis
Clostridium difficile intestinal infectious disease
disease

| colitis characterized by an overgrowth of Clostridioides difficile bacteria

| [http://www.disease-ontology.org/?id=DOID:0060185 DOID:0060185]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.410.222.310 C01.150.252.410.222.310]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.596.800 C06.405.205.596.800]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.363.800 C06.405.469.363.800]

| Pseudomembranous colitis

| File:Clostridium difficile 01.jpg

|-

| Clostridium infectious disease

| class of disease

| bacterial infectious disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3584 DOID:3584]
[http://www.disease-ontology.org/?id=DOID:0050351 DOID:0050351]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.410.222 C01.150.252.410.222]

|

|

|-

| Coats disease

| class of disease

| retinal telangiectasia
congenital vitreoretinal dysplasia
secondary glaucoma due to a proliferation and differentiation anomaly
genetic vascular disease
genetic central nervous system and retinal vascular disease
central nervous system and retinal vascular disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7765 DOID:7765]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.768.748 C11.768.748]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.823.502 C14.907.823.502]

| Coats' disease

| File:Eye of patient with Coats' disease.jpg

|-

| Coffin-Siris syndrome 1

| class of disease

| Coffin-Siris syndrome

| An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of ARID1B on chromosome 6q25.3.

| [http://www.disease-ontology.org/?id=DOID:0070042 DOID:0070042]

|

|

|

|-

| Coffin-Siris syndrome 6

| class of disease

| Coffin-Siris syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080297 DOID:0080297]

|

|

|

|-

| Cogan-Reese syndrome

| class of disease

| eye disease
iridocorneal endothelial syndrome

| eye disease characterized by variable iris atrophy, pigmented and pedunculated nodules located in iris and attachment of the iris to the cornea (peripheral anterior synechiae) and characterized by glaucoma

| [http://www.disease-ontology.org/?id=DOID:0060217 DOID:0060217]

|

|

|

|-

| Conn's syndrome

| class of disease

| hyperaldosteronism
adrenal adenoma
adrenal gland disease
disease

| adrenal adenoma characterized by over production of aldosterone

| [http://www.disease-ontology.org/?id=DOID:12028 DOID:12028]

|

| Primary aldosteronism

| File:Aldosterone-2D-skeletal.svg

|-

| Cornelia de Lange syndrome 1

| class of disease

| Cornelia de Lange syndrome
autosomal dominant disease

| Cornelia de Lange syndrome that has material basis in heterozygous mutation in the NIPBL gene, which encodes a component of the cohesin complex, on chromosome 5p13

| [http://www.disease-ontology.org/?id=DOID:0080505 DOID:0080505]

|

|

|

|-

| Cornelia de Lange syndrome 2

| class of disease

| Cornelia de Lange syndrome
X-linked dominant disease

| Cornelia de Lange syndrome that has material basis in a mutation in the SMC1A gene, which encodes a subunit of the cohesin complex, on chromosome Xp11

| [http://www.disease-ontology.org/?id=DOID:0080506 DOID:0080506]

|

|

|

|-

| Cornelia de Lange syndrome 3

| class of disease

| Cornelia de Lange syndrome
autosomal dominant disease

| A Cornelia de Lange syndrome that has material basis in heterozygous mutation in the SMC3 gene on chromosome 10q25.2.

| [http://www.disease-ontology.org/?id=DOID:0080507 DOID:0080507]

|

|

|

|-

| Cornelia de Lange syndrome 4

| class of disease

| Cornelia de Lange syndrome
autosomal dominant disease

| Cornelia de Lange syndrome that has material basis in heterozygous mutation in the RAD21 gene, which encodes a component of the cohesin complex, on chromosome 8q24

| [http://www.disease-ontology.org/?id=DOID:0080508 DOID:0080508]

|

|

|

|-

| Cornelia de Lange syndrome 5

| class of disease

| Cornelia de Lange syndrome
X-linked dominant disease

| Cornelia de Lange syndrome that has material basis in by mutation in the HDAC8 gene on chromosome Xq13

| [http://www.disease-ontology.org/?id=DOID:0080509 DOID:0080509]

|

|

|

|-

| Cortical blindness

| class of disease

| visual cortex disease
cerebral visual impairment

| human disease

| [http://www.disease-ontology.org/?id=DOID:11831 DOID:11831]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.751.941.162.250 C10.597.751.941.162.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.966.075.250 C11.966.075.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.763.941.162.250 C23.888.592.763.941.162.250]

|

|

|-

| Cowden syndrome 1

| class of disease

| autosomal dominant disease
multiple hamartoma syndrome
syndrome
disease

| inherited disorder causing tumor-like growth and increased cancer risk

| [http://www.disease-ontology.org/?id=DOID:6457 DOID:6457]

|

| Cowden syndrome

|

|-

| Cowper gland carcinoma

| class of disease

| male reproductive organ cancer
Littre gland carcinoma
carcinoma

| male reproductive organ cancer that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the Cowper's gland

| [http://www.disease-ontology.org/?id=DOID:7632 DOID:7632]

|

|

|

|-

| Crohn's colitis

| class of disease

| Crohn's disease
colitis

| inflammatory bowel disease characterized by inflammation located in colon only

| [http://www.disease-ontology.org/?id=DOID:0060192 DOID:0060192]

|

|

|

|-

| D-2-hydroxyglutaric aciduria 1

| class of disease

| D-2-hydroxyglutaric aciduria
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111351 DOID:0111351]

|

|

|

|-

| D-2-hydroxyglutaric aciduria 2

| class of disease

| autosomal dominant disease
D-2-hydroxyglutaric aciduria

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111352 DOID:0111352]

|

|

|

|-

| D-glycerate dehydrogenase deficiency

| class of disease

| primary hyperoxaluria

| disease

| [http://www.disease-ontology.org/?id=DOID:0111671 DOID:0111671]

|

|

|

|-

| D-glyceric aciduria

| class of disease

| inherited metabolic disorder
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111626 DOID:0111626]

|

|

|

|-

| D-mannitol allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger D-mannitol

| [http://www.disease-ontology.org/?id=DOID:0040019 DOID:0040019]

|

|

|

|-

| DIC in newborn

| class of disease

| disseminated intravascular coagulation

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11246 DOID:11246]

|

|

|

|-

| De Barsy syndrome

| class of disease

| inborn disorder of ornithine or proline metabolism
cutis laxa
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070143 DOID:0070143]

|

|

|

|-

| Diamond-Blackfan anemia 1

| class of disease

| Diamond-Blackfan anemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111895 DOID:0111895]

|

|

|

|-

| Diamond-Blackfan anemia 10

| class of disease

| autosomal dominant disease
Diamond-Blackfan anemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111888 DOID:0111888]

|

|

|

|-

| Diamond-Blackfan anemia 11

| class of disease

| autosomal dominant disease
Diamond-Blackfan anemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111892 DOID:0111892]

|

|

|

|-

| Diamond-Blackfan anemia 12

| class of disease

| Diamond-Blackfan anemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111882 DOID:0111882]

|

|

|

|-

| Diamond-Blackfan anemia 13

| class of disease

| Diamond-Blackfan anemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111889 DOID:0111889]

|

|

|

|-

| Diamond-Blackfan anemia 15 with mandibulofacial dysostosis

| class of disease

| Diamond-Blackfan anemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111894 DOID:0111894]

|

|

|

|-

| Diamond-Blackfan anemia 16

| class of disease

| Diamond-Blackfan anemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111893 DOID:0111893]

|

|

|

|-

| Diamond-Blackfan anemia 17

| class of disease

| autosomal dominant disease
Diamond-Blackfan anemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111880 DOID:0111880]

|

|

|

|-

| Diamond-Blackfan anemia 18

| class of disease

| Diamond-Blackfan anemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111896 DOID:0111896]

|

|

|

|-

| Diamond-Blackfan anemia 19

| class of disease

| autosomal dominant disease
Diamond-Blackfan anemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111886 DOID:0111886]

|

|

|

|-

| Diamond-Blackfan anemia 2

| class of disease

| autosomal dominant disease
Diamond-Blackfan anemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111885 DOID:0111885]

|

|

|

|-

| Diamond-Blackfan anemia 20

| class of disease

| autosomal dominant disease
Diamond-Blackfan anemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111891 DOID:0111891]

|

|

|

|-

| Diamond-Blackfan anemia 4

| class of disease

| autosomal dominant disease
Diamond-Blackfan anemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111890 DOID:0111890]

|

|

|

|-

| Diamond-Blackfan anemia 5

| class of disease

| Diamond-Blackfan anemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111883 DOID:0111883]

|

|

|

|-

| Diamond-Blackfan anemia 6

| class of disease

| Diamond-Blackfan anemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111879 DOID:0111879]

|

|

|

|-

| Diamond-Blackfan anemia 7

| class of disease

| autosomal dominant disease
Diamond-Blackfan anemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111878 DOID:0111878]

|

|

|

|-

| Diamond-Blackfan anemia 8

| class of disease

| Diamond-Blackfan anemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111881 DOID:0111881]

|

|

|

|-

| Diamond-Blackfan anemia 9

| class of disease

| Diamond-Blackfan anemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111884 DOID:0111884]

|

|

|

|-

| Diamond-blackfan anemia 3

| class of disease

| Diamond-Blackfan anemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111887 DOID:0111887]

|

|

|

|-

| Dieulafoy lesion

| class of disease

| stomach disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12070 DOID:12070]

|

| Dieulafoy's lesion

|

|-

| Doyne honeycomb retinal dystrophy

| class of disease

| drusen
genetic disease
autosomal dominant disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060745 DOID:0060745]

|

|

|

|-

| Ehlers-Danlos syndrome arthrochalasia type 1

| class of disease

| Ehlers-Danlos syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080727 DOID:0080727]

|

|

|

|-

| Ehlers-Danlos syndrome arthrochalasia type 2

| class of disease

| autosomal dominant disease
Ehlers-Danlos syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080728 DOID:0080728]

|

|

|

|-

| Ehlers-Danlos syndrome cardiac valvular type

| class of disease

| Ehlers-Danlos syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080730 DOID:0080730]

|

|

|

|-

| Ehlers-Danlos syndrome classic type 2

| class of disease

| autosomal dominant disease
Ehlers-Danlos syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080726 DOID:0080726]

|

|

|

|-

| Ehlers-Danlos syndrome classic-like 1

| class of disease

| autosomal recessive disease
Ehlers-Danlos syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080731 DOID:0080731]

|

|

|

|-

| Ehlers-Danlos syndrome classic-like 2

| class of disease

| autosomal recessive disease
Ehlers-Danlos syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080732 DOID:0080732]

|

|

|

|-

| Ehlers-Danlos syndrome dermatosparaxis type

| class of disease

| autosomal recessive disease
Ehlers-Danlos syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080733 DOID:0080733]

|

|

|

|-

| Ehlers-Danlos syndrome kyphoscoliotic type 1

| class of disease

| Ehlers-Danlos syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080734 DOID:0080734]

|

|

|

|-

| Ehlers-Danlos syndrome kyphoscoliotic type 2

| class of disease

| autosomal recessive disease
Ehlers-Danlos syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080735 DOID:0080735]

|

|

|

|-

| Ehlers-Danlos syndrome musculocontractural type 1

| class of disease

| autosomal recessive disease
Ehlers-Danlos syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080736 DOID:0080736]

|

|

|

|-

| Ehlers-Danlos syndrome musculocontractural type 2

| class of disease

| Ehlers-Danlos syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080737 DOID:0080737]

|

|

|

|-

| Ehlers-Danlos syndrome spondylodysplastic type 1

| class of disease

| autosomal recessive disease
Ehlers-Danlos syndrome
Ehlers-Danlos syndrome progeroid type

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080738 DOID:0080738]

|

|

|

|-

| Ehlers-Danlos syndrome spondylodysplastic type 3

| class of disease

| Ehlers-Danlos syndrome
Ehlers-Danlos syndrome progeroid type

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080739 DOID:0080739]

|

|

|

|-

| Ehlers-Danlos syndrome, periodontal type 2 Edspd2

| class of disease

| Ehlers-Danlos syndrome, periodontitis type
Ehlers-Danlos syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080987 DOID:0080987]

|

|

|

|-

| Ehrlich tumor carcinoma

| class of disease

| breast carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5050 DOID:5050]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.200 C04.557.470.200.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.619.169 C04.619.169]

|

|

|-

| Emery-Dreifuss muscular dystrophy 3, autosomal recessive

| class of disease

| Emery-Dreifuss muscular dystrophy
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070248 DOID:0070248]

|

|

|

|-

| Epstein-Barr virus hepatitis

| class of disease

| viral hepatitis

| viral hepatitis that results in inflammation, located in liver, has material basis in Human herpesvirus 4 and has symptom headache, has symptom fatigue, has symptom fever, has symptom abdominal pain, has symptom nausea, and has symptom jaundice

| [http://www.disease-ontology.org/?id=DOID:0050204 DOID:0050204]

|

|

|

|-

| Erdheim-Chester disease

| class of disease

| non-Langerhans-cell histiocytosis
granulomatous autoinflammatory syndrome
histiocytic and dendritic cell cancer
connective tissue neoplasm
immune disorder
disease

| rare disease

| [http://www.disease-ontology.org/?id=DOID:4329 DOID:4329]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.250.410.224 C15.604.250.410.224]

| Erdheim–Chester disease

| File:Maladie de Chester-Erdheim.png

|-

| Evans' syndrome

| class of disease

| primary thrombocytopenia
autoimmune hemolytic anemia
hemolytic anemia
autoimmune thrombocytopenia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8931 DOID:8931]

|

|

|

|-

| FTDALS3

| class of disease

| amyotrophic lateral sclerosis
frontotemporal dementia
behavioral variant of frontotemporal dementia
FTDALS1
amyotrophic lateral sclerosis and frontotemporal dementia

| amyotrophic lateral sclerosis that has material basis in mutation in the SQSTM1 gene on chromosome 5q35

| [http://www.disease-ontology.org/?id=DOID:0110068 DOID:0110068]

|

|

|

|-

| Fanconi anemia complementation group A

| class of disease

| Fanconi anemia
genetic disease
autosomal recessive disease

| Fanconi anemia that has material basis in homozygous or compound heterozygous mutation in the FANCA gene on chromosome 16q24

| [http://www.disease-ontology.org/?id=DOID:0111095 DOID:0111095]

|

|

|

|-

| Fanconi renotubular syndrome 1

| class of disease

| Fanconi syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080757 DOID:0080757]

|

|

|

|-

| Fanconi renotubular syndrome 2

| class of disease

| Fanconi syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080758 DOID:0080758]

|

|

|

|-

| Fanconi renotubular syndrome 3

| class of disease

| Fanconi syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080759 DOID:0080759]

|

|

|

|-

| Fanconi renotubular syndrome 4

| class of disease

| Fanconi syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080760 DOID:0080760]

|

|

|

|-

| Fanconi renotubular syndrome 5

| class of disease

| Fanconi syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080761 DOID:0080761]

|

|

|

|-

| Fanconi-like syndrome

| class of disease

| syndrome
genetic disease

| syndrome characterized by pancytopenia, immune deficiency and cutaneous malignancies

| [http://www.disease-ontology.org/?id=DOID:0090066 DOID:0090066]

|

|

|

|-

| Far Eastern spotted fever

| class of disease

| spotted fever

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050046 DOID:0050046]

|

|

|

|-

| Foster-Kennedy syndrome

| class of disease

| papilledema
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14555 DOID:14555]

|

|

|

|-

| Fox-Fordyce disease

| class of disease

| sweat gland disease
disease

| chronic blockage of the sweat gland ducts with a secondary, non-bacterial inflammatory response to the secretions and cellular debris in the cysts

| [http://www.disease-ontology.org/?id=DOID:1381 DOID:1381]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.946.492.285 C17.800.946.492.285]

|

|

|-

| Fraser syndrome 1

| class of disease

| Fraser syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111405 DOID:0111405]

|

|

|

|-

| Fraser syndrome 2

| class of disease

| Fraser syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111407 DOID:0111407]

|

|

|

|-

| Fraser syndrome 3

| class of disease

| Fraser syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111406 DOID:0111406]

|

|

|

|-

| French Canadian Leigh disease

| class of disease

| Leigh disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111180 DOID:0111180]

|

|

|

|-

| Frey syndrome

| class of disease

| autonomic nervous system disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:11599 DOID:11599]

|

| Frey's syndrome

|

|-

| Friedreich ataxia 1

| class of disease

|

| A Friedreich ataxia that has material basis in homozygous or compound heterozygous mutation in FXN on 9q21.1.

| [http://www.disease-ontology.org/?id=DOID:0111218 DOID:0111218]

|

|

|

|-

| Friedreich ataxia 2

| class of disease

|

| Friedreich ataxia that has material basis in mutation in the 9p23-p11 chromosome region

| [http://www.disease-ontology.org/?id=DOID:0111219 DOID:0111219]

|

|

|

|-

| Froelich syndrome

| class of disease

| hypothalamic disease

| hypothalamic disease that is characterized by endocrine dysfunction of the hypothalamic gland resulting in delayed puberty, small testes, and obesity

| [http://www.disease-ontology.org/?id=DOID:6676 DOID:6676]

|

| Adiposogenital dystrophy

|

|-

| Fuchs' endothelial dystrophy

| class of disease

| corneal endothelial dystrophy
disease

| corneal dystrophy characterized by accumulation of focal outgrowths (guttae) and thickening of Descemet's membrane, leading to corneal edema and loss of vision

| [http://www.disease-ontology.org/?id=DOID:11555 DOID:11555]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.204.236.438 C11.204.236.438]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.270.162.438 C11.270.162.438]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.290.162.410 C16.320.290.162.410]

| Fuchs' dystrophy

|

|-

| Fuchs' heterochromic uveitis

| class of disease

| uveitis
syndrome

| syndrome that is a chronic unilateral (or rarely bilateral) iridocyclitis appearing with the triad of heterochromia, predisposition to cataracts and glaucoma, and keratitic percipitates on the posterior corneal surface

| [http://www.disease-ontology.org/?id=DOID:9375 DOID:9375]

|

| Fuchs heterochromic iridocyclitis

|

|-

| GM1 gangliosidosis type 1

| class of disease

| gangliosidosis GM1

| GM1 gangliosidosis type 1 is the severe infantile form of GM1 gangliosidosis (see this term) with variable neurological and systemic manifestations

| [http://www.disease-ontology.org/?id=DOID:0080502 DOID:0080502]

|

|

|

|-

| GM1 gangliosidosis type 2

| class of disease

| gangliosidosis GM1

| GM1 gangliosidosis that is characterized by slowly progressive generalized neurodegeneration and mild skeletal changes, with onset between 7 months and 3 years of age

| [http://www.disease-ontology.org/?id=DOID:0080501 DOID:0080501]

|

|

|

|-

| GM2 gangliosidosis

| class of disease

| gangliosidosis
nervous system heredodegenerative disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3321 DOID:3321]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.163.100.435.825.300.300 C10.228.140.163.100.435.825.300.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.189.435.825.300.300 C16.320.565.189.435.825.300.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.398.641.803.350.300 C16.320.565.398.641.803.350.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.595.554.825.300.300 C16.320.565.595.554.825.300.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.132.100.435.825.300.300 C18.452.132.100.435.825.300.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.563.641.803.350.300 C18.452.584.563.641.803.350.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.189.435.825.300.300 C18.452.648.189.435.825.300.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.398.641.803.350.300 C18.452.648.398.641.803.350.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.595.554.825.300.300 C18.452.648.595.554.825.300.300]

|

|

|-

| GNE myopathy

| class of disease

| autosomal recessive disease
muscular disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080718 DOID:0080718]

|

|

|

|-

| GRID2-related autosomal dominant spinocerebellar ataxia

| class of disease

| spinocerebellar ataxia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050988 DOID:0050988]

|

|

|

|-

| GRN-related frontotemporal lobar degeneration with Tdp43 inclusions

| class of disease

| frontotemporal lobar degeneration
frontotemporal dementia
primary progressive aphasia
genetic disease
autosomal dominant disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060672 DOID:0060672]

|

|

|

|-

| Galloway-Mowat syndrome 2

| class of disease

| Galloway-Mowat syndrome
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080244 DOID:0080244]

|

|

|

|-

| Galloway-Mowat syndrome 3

| class of disease

| Galloway-Mowat syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080245 DOID:0080245]

|

|

|

|-

| Galloway-Mowat syndrome 4

| class of disease

| Galloway-Mowat syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080246 DOID:0080246]

|

|

|

|-

| Galloway-Mowat syndrome 5

| class of disease

| Galloway-Mowat syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080247 DOID:0080247]

|

|

|

|-

| Gasserian ganglion meningioma

| class of disease

| meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7635 DOID:7635]

|

|

|

|-

| Gaucher's disease perinatal lethal

| class of disease

| Gaucher's disease
genetic disease

| Gaucher's Disease characterized by perinatal lethality and rapid progression of neurological deterioration that has material basis in an autosomal recessive mutation of GBA on chromosome 1q22

| [http://www.disease-ontology.org/?id=DOID:0110960 DOID:0110960]

|

|

|

|-

| Gaucher's disease type I

| class of disease

| Gaucher's disease
genetic disease

| Gaucher's disease characterized by absence of primary central nervous system involvement that has material basis in a mutation of GBA on chromosome 1q22

| [http://www.disease-ontology.org/?id=DOID:0110957 DOID:0110957]

|

|

|

|-

| Gaucher's disease type II

| class of disease

| Gaucher's disease
genetic disease

| Gaucher's disease characterized by rapid neurologic deterioration with cranial nerve and extrapyramidal tract involvement that has material basis in an autosomal recessive mutation of GBA on chromosome 1q22

| [http://www.disease-ontology.org/?id=DOID:0110958 DOID:0110958]

|

|

|

|-

| Gaucher's disease type III

| class of disease

| Gaucher's disease
genetic disease

| Gaucher's disease characterized by later onset and slower progession of neurological deterioration compared to type II that has material basis in an autosomal recessive mutation of GBA on chromosome 1q22

| [http://www.disease-ontology.org/?id=DOID:0110959 DOID:0110959]

|

|

|

|-

| Geleophysic dysplasia 2

| class of disease

| geleophysic dysplasia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111726 DOID:0111726]

|

|

|

|-

| Gerstmann syndrome

| class of disease

| neurological disorder
disease

| nervous system disease that results from damage located in left parietal lobe, has symptom agraphia, has symptom acalculia, has symptom finger agnosia

| [http://www.disease-ontology.org/?id=DOID:4969 DOID:4969]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.606.762.100.300 C10.597.606.762.100.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.604.764.100.300 C23.888.592.604.764.100.300]

|

| File:Gray728.svg

|-

| Gilbert syndrome

| class of disease

| bilirubin metabolic disorder
disease

| metabolic disorder in which the liver processes bilirubin slowly

| [http://www.disease-ontology.org/?id=DOID:2739 DOID:2739]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.300.528 C16.320.565.300.528]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.300.528 C18.452.648.300.528]

|

| File:Bilirubin.svg

|-

| Glanzmann's thrombasthenia

| class of disease

| blood platelet disease
inherited blood coagulation disease
rare hemorrhagic disorder due to a qualitative platelet defect
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:2219 DOID:2219]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100.100.820 C15.378.100.100.820]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.140.810 C15.378.140.810]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463.810 C15.378.463.810]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.099.820 C16.320.099.820]

|

|

|-

| Good syndrome

| class of disease

| agammaglobulinemia
combined immunodeficiency

| agammaglobulinemia that is a condition where there is co-occurrence of deficient cell-mediated immunity and benign thymoma

| [http://www.disease-ontology.org/?id=DOID:0060028 DOID:0060028]

|

|

|

|-

| Graves' disease

| class of disease

| autoimmune disease of endocrine system

| autoimmune disease of endocrine system that involves production of excessive amount of thyroid hormones, located in thyroid gland

| [http://www.disease-ontology.org/?id=DOID:12361 DOID:12361]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.675.349.500 C11.675.349.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.874.283.605 C19.874.283.605]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.874.397.370 C19.874.397.370]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.555 C20.111.555]

|

|

|-

| Griscelli syndrome

| class of disease

| autosomal recessive disease
integumentary system disease

| autosomal recessive disease characterized by silvery gray sheen of the hair and hypopigmentation of the skin

| [http://www.disease-ontology.org/?id=DOID:0060831 DOID:0060831]

|

|

|

|-

| Griscelli syndrome type 2

| class of disease

| Griscelli syndrome

| A Griscelli syndrome characterized by silvery gray sheen of the hair, hypopigmentation of the skin and immunodeficiency with or without neurologic impairment that has material basis in mutation in the RAB27A gene on chromosome 15q21.3.

| [http://www.disease-ontology.org/?id=DOID:0060833 DOID:0060833]

|

|

|

|-

| Griscelli syndrome type 3

| class of disease

| Griscelli syndrome

| Griscelli syndrome characterized by isolated silvery gray sheen of the hair and hypopigmentation of the skin that has material basis in mutation in the MLPH or MYO5A genes

| [http://www.disease-ontology.org/?id=DOID:0060834 DOID:0060834]

|

|

|

|-

| Gulf War syndrome

| class of disease

| syndrome
disease

| illlnesses affecting Gulf War Vets

| [http://www.disease-ontology.org/?id=DOID:4491 DOID:4491]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C24.653 C24.653]

|

| File:Pyridostigmine.svg

|-

| H syndrome

| class of disease

| histiocytosis
autosomal recessive disease
syndrome

| genetic condition

| [http://www.disease-ontology.org/?id=DOID:0111278 DOID:0111278]

|

|

|

|-

| HCL-V

| class of disease

| hairy cell leukemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:713 DOID:713]

|

|

|

|-

| HELLP syndrome

| class of disease

| severe pre-eclampsia
disease

| severe pre-eclampsia characterized by hemolysis, elevated liver enzyme and low platelet count

| [http://www.disease-ontology.org/?id=DOID:13133 DOID:13133]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.395.186 C13.703.395.186]

|

|

|-

| Haemodialysis-associated amyloidosis

| class of disease

| amyloidosis
Dialytrauma
ABeta2M amyloidosis
acquired metabolic disease
kidney disease

| #946;2M) deposits in the musculoskeletal system leading to carpal tunnel syndrome (CTS), chronic arthropathy, cystic bone lesions, destructive osteoarthropathy, and pathologic fractures

| [http://www.disease-ontology.org/?id=DOID:0080928 DOID:0080928]

|

|

|

|-

| Heart failure with preserved ejection fraction

| class of disease

| heart failure
congestive heart failure

| congestive heart failure wherein the amount of blood pumped from the heart's left ventricle with each beat (ejection fraction) is greater than 50%

| [http://www.disease-ontology.org/?id=DOID:9775 DOID:9775]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.434.611 C14.280.434.611]

|

|

|-

| Heimler syndrome 1

| class of disease

| deafness-enamel hypoplasia-nail defects syndrome
peroxisomal biogenesis disorder
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080623 DOID:0080623]

|

|

|

|-

| Heimler syndrome 2

| class of disease

| deafness-enamel hypoplasia-nail defects syndrome
peroxisomal biogenesis disorder
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080624 DOID:0080624]

|

|

|

|-

| Heinz body anemia

| class of disease

| congenital hemolytic anemia
congenital nonspherocytic hemolytic anemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111363 DOID:0111363]

|

|

|

|-

| Henoch-Schoenlein purpura

| class of disease

| hypersensitivity vasculitis
nonthrombocytopenic purpura
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11123 DOID:11123]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.940.777 C14.907.940.777]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100.802.375 C15.378.100.802.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463.515.580 C15.378.463.515.580]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.520.600 C20.543.520.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.414.950.375 C23.550.414.950.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.885.687.375 C23.888.885.687.375]

| Henoch–Schönlein purpura

| File:Henoch-schonlein-purpura.jpg

|-

| Her2-receptor negative breast cancer

| class of disease

| breast cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060080 DOID:0060080]

|

|

|

|-

| Her2-receptor positive breast cancer

| class of disease

| breast cancer
breast carcinoma by gene expression profile
Hormone receptor positive breast tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060079 DOID:0060079]

|

|

|

|-

| Hermansky-Pudlak syndrome 1

| class of disease

| Hermansky-Pudlak syndrome

| A Hermansky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the HPS1 gene on chromosome 10q24.

| [http://www.disease-ontology.org/?id=DOID:0060539 DOID:0060539]

|

|

|

|-

| Hermansky-Pudlak syndrome 2

| class of disease

| Hermansky-Pudlak syndrome

| A Hermansky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the gene encoding the beta-3A subunit of the AP3 complex (AP3B1) on chromosome 5q14.1.

| [http://www.disease-ontology.org/?id=DOID:0060540 DOID:0060540]

|

|

|

|-

| Hermansky-Pudlak syndrome 3

| class of disease

| Hermansky-Pudlak syndrome

| Hermasky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the HPS3 gene on chromosome 3q24

| [http://www.disease-ontology.org/?id=DOID:0060541 DOID:0060541]

|

|

|

|-

| Hermansky-Pudlak syndrome 4

| class of disease

| Hermansky-Pudlak syndrome

| A Hermansky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the HPS4 gene on chromosome 22q12.1.

| [http://www.disease-ontology.org/?id=DOID:0060542 DOID:0060542]

|

|

|

|-

| Hermansky-Pudlak syndrome 5

| class of disease

| Hermansky-Pudlak syndrome

| Hermansky-Pudlak syndrome that has material basis in homozygous mutation in the HPS5 gene on chromosome 11p14

| [http://www.disease-ontology.org/?id=DOID:0060543 DOID:0060543]

|

|

|

|-

| Hermansky-Pudlak syndrome 6

| class of disease

| Hermansky-Pudlak syndrome

| Hermansky-Pudlak syndrome that has material basis in homozygous or compound heterozygous mutation in the HPS6 gene on chromosome 10q24

| [http://www.disease-ontology.org/?id=DOID:0060544 DOID:0060544]

|

|

|

|-

| Hermansky-Pudlak syndrome 7

| class of disease

| Hermansky-Pudlak syndrome

| A Hermansky-Pudlak syndrome that has material basis in homozygous mutation in the DTNBP1 gene on chromosome 6p22.3.

| [http://www.disease-ontology.org/?id=DOID:0060545 DOID:0060545]

|

|

|

|-

| Hermansky-Pudlak syndrome 8

| class of disease

| Hermansky-Pudlak syndrome

| Hermansky-Pudlak syndrome that has material basis in homozygous mutation in the BLOC1S3 gene on chromosome 19q13

| [http://www.disease-ontology.org/?id=DOID:0060546 DOID:0060546]

|

|

|

|-

| Hermansky-Pudlak syndrome 9

| class of disease

| Hermansky-Pudlak syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060547 DOID:0060547]

|

|

|

|-

| Hirata disease

| class of disease

| autoimmune disease of endocrine system
immune disorder
hyperinsulinemic hypoglycemia

| autoimmune disease of endocrine system characterized by hypoglycemia caused by antibodies to insulin

| [http://www.disease-ontology.org/?id=DOID:0040100 DOID:0040100]

|

|

|

|-

| Hodgkin lymphoma

| class of disease
symptom or sign

| lymphoma
disease

| lymphoma that is marked classically by the presence of Reed-Sternberg cells

| [http://www.disease-ontology.org/?id=DOID:8567 DOID:8567]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386.355 C04.557.386.355]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.569.355 C15.604.515.569.355]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.761.355 C20.683.515.761.355]

| Hodgkin's lymphoma

| File:Hodgkin lymphoma (1) mixed cellulary type.jpg

|-

| Hodgkin's granuloma

| class of disease

| Hodgkin lymphoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:8651 DOID:8651]

|

|

|

|-

| Hodgkin's lymphoma, lymphocytic depletion

| class of disease

| Hodgkin lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8628 DOID:8628]

|

|

|

|-

| Hodgkin's lymphoma, lymphocytic-histiocytic predominance

| class of disease

| Hodgkin lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8543 DOID:8543]

|

|

|

|-

| Hodgkin's lymphoma, mixed cellularity

| class of disease

| Hodgkin lymphoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:8654 DOID:8654]

|

|

|

|-

| Hodgkin's lymphoma, nodular sclerosis

| class of disease

| Hodgkin lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8838 DOID:8838]

|

|

|

|-

| Hodgkin's paragranuloma

| class of disease

| Hodgkin lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8642 DOID:8642]

|

|

|

|-

| Horner's syndrome

| class of disease

| autonomic neuropathy
disease

| A disease characterized by miosis (a constricted pupil), partial ptosis (a weak, droopy eyelid), apparent anhydrosis (decreased sweating), with apparent enophthalmos (inset eyeball)

| [http://www.disease-ontology.org/?id=DOID:11486 DOID:11486]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.177.350 C10.177.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.690.362.500 C10.597.690.362.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.710.528.500 C11.710.528.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.708.362.500 C23.888.592.708.362.500]

| Horner's syndrome

| File:Miosis.jpg

|-

| IDH-wildtype anaplastic astrocytoma

| class of disease

| anaplastic astrocytoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080876 DOID:0080876]

|

|

|

|-

| IGSF1 deficiency syndrome

| class of disease

| central congenital hypothyroidism
X-linked recessive disease
syndrome

| X-linked disease characterized by hypothyroidism that is present at birth, delayed testosterone increase in puberty, and testicular enlargement in adulthood that has material basis in mutation of the IGSF1 gene on chromosome Xq26

| [http://www.disease-ontology.org/?id=DOID:0111140 DOID:0111140]

|

|

|

|-

| IgG4-related disease

| class of disease

| autoimmune connective tissue disorder
autoimmune disease

| systemic fibroinflammatory disease, associated with elevated serum IgG4 levels in about 60% of cases

| [http://www.disease-ontology.org/?id=DOID:0080356 DOID:0080356]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.572 C20.111.572]

| IgG4-related disease

| File:Lesions of rectus muscles and nerves.jpg

|-

| Indian plum allergy

| class of disease

| fruit allergy

| fruit allergy triggered by Ziziphus mauritiana plant fruit food product.

| [http://www.disease-ontology.org/?id=DOID:0060507 DOID:0060507]

|

|

|

|-

| Indian prawn allergy

| class of disease

| shrimp allergy
crustacean allergy

| crustacean allergy triggered by Fenneropenaeus indicus

| [http://www.disease-ontology.org/?id=DOID:0060527 DOID:0060527]

|

|

|

|-

| Indian tick typhus

| class of disease

| spotted fever

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050042 DOID:0050042]

|

|

|

|-

| Israeli tick typhus

| class of disease

| spotted fever

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050043 DOID:0050043]

|

|

|

|-

| Jaccoud's syndrome

| class of disease

| autoimmune disease
joint disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13080 DOID:13080]

|

| Jaccoud arthropathy

|

|-

| Japanese spotted fever

| class of disease

| spotted fever

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050050 DOID:0050050]

|

|

|

|-

| Jewett-Marshall bladder cancer

| class of disease

| bladder carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7315 DOID:7315]

|

|

|

|-

| Joubert syndrome 1

| class of disease

| Joubert syndrome

| Joubert syndrome that has material basis in homozygous mutation in the INPP5E gene on chromosome 9q34

| [http://www.disease-ontology.org/?id=DOID:0110980 DOID:0110980]

|

|

|

|-

| Joubert syndrome 10

| class of disease

| Joubert syndrome
Joubert syndrome with orofaciodigital defect
X-linked recessive disease

| A Joubert syndrome that has material basis in X-linked recessive inheritance of mutation in the OFD1 gene on chromosome Xp22.2.

| [http://www.disease-ontology.org/?id=DOID:0110981 DOID:0110981]

|

|

|

|-

| Joubert syndrome 13

| class of disease

| Joubert syndrome

| Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the TCTN1 gene on chromosome 12q24

| [http://www.disease-ontology.org/?id=DOID:0110982 DOID:0110982]

|

|

|

|-

| Joubert syndrome 14

| class of disease

| Joubert syndrome
Joubert syndrome with oculorenal defect
Joubert syndrome with ocular defect

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110983 DOID:0110983]

|

|

|

|-

| Joubert syndrome 15

| class of disease

| Joubert syndrome
Joubert syndrome with ocular defect

| Joubert syndrome characterized by ataxia, hypotonia, delayed psychomotor development, and variable mental retardation that has material basis in homozygous mutation in the CEP41 gene on chromosome 7q32

| [http://www.disease-ontology.org/?id=DOID:0110984 DOID:0110984]

|

|

|

|-

| Joubert syndrome 17

| class of disease

| Joubert syndrome

| Joubert syndrome characterized by episodic hyperpnea, abnormal eye movements, ataxia, and global psychomotor retardation that has material basis in compound heterozygous mutation in the C5ORF42 gene on chromosome 5p13

| [http://www.disease-ontology.org/?id=DOID:0110986 DOID:0110986]

|

|

|

|-

| Joubert syndrome 18

| class of disease

| Joubert syndrome
Joubert syndrome with orofaciodigital defect

| Joubert syndrome that has material basis in homozygous mutation in the TCTN3 gene on chromosome 10q24

| [http://www.disease-ontology.org/?id=DOID:0110987 DOID:0110987]

|

|

|

|-

| Joubert syndrome 20

| class of disease

| Joubert syndrome
Joubert syndrome with ocular defect

| Joubert syndrome that has material basis in compound heterozygous mutation in the TMEM231 gene on chromosome 16q23

| [http://www.disease-ontology.org/?id=DOID:0110989 DOID:0110989]

|

|

|

|-

| Joubert syndrome 21

| class of disease

| Joubert syndrome
Joubert syndrome with Jeune asphyxiating thoracic dystrophy

| Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the CSPP1 gene on chromosome 8q13

| [http://www.disease-ontology.org/?id=DOID:0110990 DOID:0110990]

|

|

|

|-

| Joubert syndrome 22

| class of disease

| Joubert syndrome
Joubert syndrome with orofaciodigital defect

| Joubert syndrome that has material basis in homozygous mutation in the PDE6D gene on chromosome 2q37

| [http://www.disease-ontology.org/?id=DOID:0110991 DOID:0110991]

|

|

|

|-

| Joubert syndrome 23

| class of disease

| Joubert syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110992 DOID:0110992]

|

|

|

|-

| Joubert syndrome 24

| class of disease

| Joubert syndrome

| Joubert syndrome characterized by delayed psychomotor development and molar tooth sign on brain MRI that has material basis in homozygous mutation in the TCTN2 gene on chromosome 12q24

| [http://www.disease-ontology.org/?id=DOID:0110993 DOID:0110993]

|

|

|

|-

| Joubert syndrome 25

| class of disease

| Joubert syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110994 DOID:0110994]

|

|

|

|-

| Joubert syndrome 26

| class of disease

| Joubert syndrome

| Joubert syndrome characterized by global developmental delay and cerebellar hypoplasia that has material basis in homozygous mutation in the KIAA0556 gene on chromosome 16p12

| [http://www.disease-ontology.org/?id=DOID:0110995 DOID:0110995]

|

|

|

|-

| Joubert syndrome 27

| class of disease

| Joubert syndrome

| Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the B9D1 gene on chromosome 17p11

| [http://www.disease-ontology.org/?id=DOID:0110996 DOID:0110996]

|

|

|

|-

| Joubert syndrome 28

| class of disease

| Joubert syndrome
Joubert syndrome with ocular defect

| Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the MKS1 gene on chromosome 17q23

| [http://www.disease-ontology.org/?id=DOID:0110997 DOID:0110997]

|

|

|

|-

| Joubert syndrome 29

| class of disease

| Joubert syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080276 DOID:0080276]

|

|

|

|-

| Joubert syndrome 30

| class of disease

| Joubert syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080275 DOID:0080275]

|

|

|

|-

| Joubert syndrome 31

| class of disease

| Joubert syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080277 DOID:0080277]

|

|

|

|-

| Joubert syndrome 6

| class of disease

| Joubert syndrome

| Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the TMEM67 on chromosome 8q22

| [http://www.disease-ontology.org/?id=DOID:0111001 DOID:0111001]

|

|

|

|-

| Joubert syndrome 7

| class of disease

| Joubert syndrome

| A Joubert syndrome that has material basis in mutation in the RPGRIP1L gene on chromosome 16q12.2.

| [http://www.disease-ontology.org/?id=DOID:0111002 DOID:0111002]

|

|

|

|-

| Joubert syndrome 8

| class of disease

| Joubert syndrome

| A Joubert syndrome that has material basis in mutation in the ARL13B gene on chromosome 3q11.1-q11.2

| [http://www.disease-ontology.org/?id=DOID:0111003 DOID:0111003]

|

|

|

|-

| Kallmann syndrome

| class of disease

| hypogonadotropic hypogonadism
disease

| A form of hypogonadotropic hypogonadism which is also accompanied by a total lack or partial loss in the sense of smell. The condition affects both males and females and causes a failure in puberty and infertility.

| [http://www.disease-ontology.org/?id=DOID:3614 DOID:3614]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.706.316.096.750 C12.706.316.096.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.875.253.096.750 C13.351.875.253.096.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.316.096.750 C16.131.939.316.096.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.467 C16.320.467]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.119.096.750 C19.391.119.096.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.482.600 C19.391.482.600]

| Kallmann syndrome

|

|-

| Kanzaki disease

| class of disease

| Schindler disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112319 DOID:0112319]

|

|

|

|-

| Kartagener syndrome

| class of disease

| primary ciliary dyskinesia
situs inversus
disease

| primary ciliary dyskinesia that is characterized by sinusitis, bronchiectasis and situs inversus with dextrocardia resulting from dysfunction of the cilia during embryologic development

| [http://www.disease-ontology.org/?id=DOID:0050144 DOID:0050144]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.127.384.500 C08.127.384.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.200.531 C08.200.531]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.695.501 C08.695.501]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.150.531 C09.150.531]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.240.400.280.500 C14.240.400.280.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.400.280.500 C14.280.400.280.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.077.245.500.531 C16.131.077.245.500.531]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.240.400.280.500 C16.131.240.400.280.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.740.501 C16.131.740.501]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.810.250.500 C16.131.810.250.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.184.500.531 C16.320.184.500.531]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.480 C16.320.480]

| Kartagener syndrome

| File:Kartagener.svg

|-

| Kawasaki disease

| class of disease

| lymphadenitis
immune disorder
predominantly medium-vessel vasculitis
disease

| human disease in which blood vessels throughout the body become inflamed

| [http://www.disease-ontology.org/?id=DOID:13378 DOID:13378]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.940.560 C14.907.940.560]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.560 C15.604.560]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.862.560 C17.800.862.560]

| Kawasaki disease

| File:Kawasaki Disease.png

|-

| Kelley–Seegmiller syndrome

| class of disease

| hypoxanthine-guanine phosphoribosyltransferase deficiency
hyperuricemia
X-linked recessive disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112127 DOID:0112127]

|

|

|

|-

| Kimura disease

| class of disease

| skin disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7365 DOID:7365]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.815.178 C07.465.815.178]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.553.231.774 C15.378.553.231.774]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.315.459 C15.604.315.459]

|

|

|-

| King Denborough syndrome

| class of disease

| autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080990 DOID:0080990]

|

|

|

|-

| Klatskin's tumor

| class of disease

| intrahepatic cholangiocarcinoma
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4927 DOID:4927]
[http://www.disease-ontology.org/?id=DOID:5246 DOID:5246]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.450.500 C04.557.470.200.025.450.500]

|

|

|-

| Kleefstra syndrome 1

| class of disease

| Kleefstra syndrome
autosomal dominant disease
chromosomal deletion syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060352 DOID:0060352]

|

|

|

|-

| Kleefstra syndrome 2

| class of disease

| autosomal dominant disease
Kleefstra syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080598 DOID:0080598]

|

|

|

|-

| Klippel-Feil syndrome 1

| class of disease

| Klippel-Feil syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080589 DOID:0080589]

|

|

|

|-

| Klippel-Feil syndrome 2

| class of disease

| Klippel-Feil syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080590 DOID:0080590]

|

|

|

|-

| Klippel-Feil syndrome 3, autosomal dominant

| class of disease

| autosomal dominant disease
Klippel-Feil syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080591 DOID:0080591]

|

|

|

|-

| Klüver–Bucy syndrome

| class of disease

| impulse control disorder
disease

| syndrome resulting from bilateral lesions of the medial temporal lobe

| [http://www.disease-ontology.org/?id=DOID:2510 DOID:2510]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.380.326 C10.228.140.380.326]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.615.400.431 F03.615.400.431]

|

|

|-

| Kohler's disease

| class of disease
symptom or sign

| osteochondrosis
foot diseases
disease

| osteochondrosis that results in death and collapse located in navicular bone of foot

| [http://www.disease-ontology.org/?id=DOID:11760 DOID:11760]

|

| Köhler disease

| File:Köhler I.png

|-

| Korean hemorrhagic fever

| class of disease

| hemorrhagic fever with renal syndrome

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050200 DOID:0050200]

|

|

|

|-

| Kuhnt-Junius degeneration

| class of disease

| degeneration of macula and posterior pole

| human disease

| [http://www.disease-ontology.org/?id=DOID:10873 DOID:10873]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.768.585.439.622 C11.768.585.439.622]

|

|

|-

| Kunjin encephalitis

| class of disease

| West Nile encephalitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050174 DOID:0050174]

|

|

|

|-

| Kuru

| class of disease

| transmissible spongiform encephalopathy
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:648 DOID:648]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.228.800.435 C10.228.228.800.435]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.843.625 C10.574.843.625]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.207.800.435 C01.207.800.435]

| Kuru (disease)

| File:Fore child in advanced kuru stage.png

|-

| L-cell glucagon-like peptide producing tumor

| class of disease

| gastrointestinal neuroendocrine benign tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7402 DOID:7402]

|

|

|

|-

| L1 syndrome

| class of disease

| X-linked intellectual disability
hereditary spastic paraplegia
X-linked complex spastic paraplegia
nervous system heredodegenerative disease
X-linked recessive disease

| hereditary spastic paraplegia that is characterized by hydrocephalus, spasticity of the lower limbs, adducted thumbs, aphasia, seizures, agenesis of the corpus callosum and intellectual disability in the mild to moderate range

| [http://www.disease-ontology.org/?id=DOID:0060246 DOID:0060246]
[http://www.disease-ontology.org/?id=DOID:0110762 DOID:0110762]

|

|

|

|-

| LEOPARD syndrome 1

| class of disease

| LEOPARD syndrome

| LEOPARD syndrome that has material basis in heterozygous mutation in the PTPN11 gene on chromosome 12q24

| [http://www.disease-ontology.org/?id=DOID:0080548 DOID:0080548]

|

|

|

|-

| LEOPARD syndrome 2

| class of disease

| LEOPARD syndrome

| LEOPARD syndrome that has material basis in heterozygous mutation in the RAF1 gene on chromosome 3p25

| [http://www.disease-ontology.org/?id=DOID:0080549 DOID:0080549]

|

|

|

|-

| LEOPARD syndrome 3

| class of disease

| LEOPARD syndrome

| LEOPARD syndrome that has material basis in heterozygous mutation in the BRAF gene on chromosome 7q34

| [http://www.disease-ontology.org/?id=DOID:0080550 DOID:0080550]

|

|

|

|-

| Lambert-Eaton myasthenic syndrome

| class of disease

| neuromuscular junction disease
channelopathy
immune-mediated acquired neuromuscular junction disease
paraneoplastic neurologic syndrome
autoimmune disease of musculoskeletal system
autoimmune disease of peripheral nervous system
disease

| an autoimmune, presynaptic disorder of neuromuscular transmission characterized by fluctuating muscle weakness and autonomic dysfunction frequently associated with small-cell lung cancer (SCLC)

| [http://www.disease-ontology.org/?id=DOID:0050214 DOID:0050214]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.614.550.500.225 C04.588.614.550.500.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.730.856.490.225 C04.730.856.490.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.114.656.150 C10.114.656.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.781.588.225 C10.574.781.588.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.758.725.150 C10.668.758.725.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.258.500.150 C20.111.258.500.150]

|

| File:Synapse diag3.png

|-

| Langerhans cell sarcoma

| class of disease

| dendritic cell tumor
leukocyte disease
histiocytic and dendritic cell cancer
sarcoma

| histiocytic and dendritic cell cancer that derives from the lymph nodes, derives from the skin, derives from the liver, derives from the spleen and derives from bones

| [http://www.disease-ontology.org/?id=DOID:7146 DOID:7146]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.227.500 C04.557.227.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.250.390.500 C15.604.250.390.500]

|

|

|-

| Langerhans-cell histiocytosis

| class of disease

| histiocytosis
disease

| disease involving clonal proliferation of Langerhans cells

| [http://www.disease-ontology.org/?id=DOID:2571 DOID:2571]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.483.375 C08.381.483.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.250.400 C15.604.250.400]

| Langerhans cell histiocytosis

| File:Hans-Schuller-Christian.jpg

|-

| Leber congenital amaurosis 1

| class of disease

| Leber congenital amaurosis
genetic disease
autosomal recessive disease

| Leber congenital amaurosis characterized by severe cone-rod dystrophy with photophobia, high hyperopia, and poor but stable vision with no visual improvement and that has material basis in mutation in the GUCY2D gene on chromosome 17p13

| [http://www.disease-ontology.org/?id=DOID:0110078 DOID:0110078]

|

|

|

|-

| Leber hereditary optic neuropathy with demyelinating disease of CNS

| class of disease

| Leber plus disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111756 DOID:0111756]

|

|

|

|-

| Leber optic atrophy and dystonia

| class of disease

| Leber plus disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111755 DOID:0111755]

|

|

|

|-

| Leber plus disease

| class of disease

| Leber hereditary optic neuropathy
syndrome

|

| [http://www.disease-ontology.org/?id=DOID:0111754 DOID:0111754]

|

|

|

|-

| Lenz-Majewski hyperostotic dwarfism

| class of disease

| autosomal dominant disease
syndrome
osteochondrodysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111507 DOID:0111507]

|

|

|

|-

| Lewy body dementia

| class of disease

| synucleinopathy
dementia

| type of dementia

| [http://www.disease-ontology.org/?id=DOID:12217 DOID:12217]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.079.862.400 C10.228.140.079.862.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.380.422 C10.228.140.380.422]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.662.600.200 C10.228.662.600.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.531 C10.574.531]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.615.400.512 F03.615.400.512]

| Lewy body dementia

| File:Lewy Koerperchen.JPG

|-

| Leydig cell tumor

| class of disease

| testicular sex cord-stromal neoplasm
sex cord-gonadal stromal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2696 DOID:2696]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.475.750.847.249 C04.557.475.750.847.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.762.500.249 C04.588.322.762.500.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.945.440.915.500.249 C04.588.945.440.915.500.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.260.937.500.249 C12.294.260.937.500.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.758.409.937.500.249 C12.758.409.937.500.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.762.500.249 C19.344.762.500.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.829.782.500.249 C19.391.829.782.500.249]

|

|

|-

| Li-Fraumeni syndrome 1

| class of disease

| Li-Fraumeni syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111503 DOID:0111503]

|

|

|

|-

| Li-Fraumeni syndrome 2

| class of disease

| Li-Fraumeni syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111504 DOID:0111504]

|

|

|

|-

| Libman–Sacks endocarditis

| class of disease

| marantic endocarditis
autoimmune disease of cardiovascular system
endocarditis
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080740 DOID:0080740]

|

|

|

|-

| Lisch epithelial corneal dystrophy

| class of disease

| epithelial and subepithelial dystrophy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060450 DOID:0060450]

|

|

|

|-

| Littre gland carcinoma

| class of disease

| male reproductive organ cancer
male urethral cancer
carcinoma

| male reproductive organ cancer that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the Littre glands

| [http://www.disease-ontology.org/?id=DOID:6721 DOID:6721]

|

|

|

|-

| Livedoid vasculitis

| class of disease

| vasculitis

| vasculitis with purpuric ulcers

| [http://www.disease-ontology.org/?id=DOID:0040099 DOID:0040099]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.355.830.573 C14.907.355.830.573]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.862.406 C17.800.862.406]

| Livedoid vasculitis

|

|-

| Loeffler endocarditis

| class of disease

| restrictive cardiomyopathy
non-familial restrictive cardiomyopathy
disease

| restrictive cardiomyopathy that affects the endocardium and occurs with white blood cell proliferation, specifically of eosinophils

| [http://www.disease-ontology.org/?id=DOID:396 DOID:396]

|

|

|

|-

| Loeffler syndrome

| class of disease

| eosinophilic pneumonia
Acute eosinophilic pneumonia
allergy
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9503 DOID:9503]

|

|

|

|-

| Loeys-Dietz syndrome 1

| class of disease

| Loeys-Dietz syndrome

| Loeys-Dietz syndrome that has material basis in heterozygous mutation in the TGFBR1 gene on chromosome 9q22

| [http://www.disease-ontology.org/?id=DOID:0070235 DOID:0070235]

|

|

|

|-

| Loeys-Dietz syndrome 2

| class of disease

| Loeys-Dietz syndrome

| Loeys-Dietz syndrome that has material basis in heterozygous mutation in the TGFBR2 gene on chromosome 3p24

| [http://www.disease-ontology.org/?id=DOID:0070234 DOID:0070234]

|

|

|

|-

| Loeys-Dietz syndrome 4

| class of disease

| Loeys-Dietz syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070233 DOID:0070233]

|

|

|

|-

| Lown-Ganong-Levine syndrome

| class of disease

| syndrome
pre-excitation syndrome
genetic cardiac rhythm disease
disease

| syndrome that involves pre-excitation of the ventricles due to an accessory pathway providing an abnormal electrical communication from the atria to the ventricles

| [http://www.disease-ontology.org/?id=DOID:13087 DOID:13087]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.067.780.560 C14.280.067.780.560]

| Lown-Ganong-Levine syndrome

|

|-

| Lynch syndrome

| class of disease

| autosomal dominant disease
hereditary neoplastic syndromes
colorectal cancer
neoplasm
syndrome
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3883 DOID:3883]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.476.411.307.190 C04.588.274.476.411.307.190]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.700.250 C04.700.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.371.411.307.190 C06.301.371.411.307.190]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.249.411.307.190 C06.405.249.411.307.190]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.158.356.190 C06.405.469.158.356.190]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.491.307.190 C06.405.469.491.307.190]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.700.250 C16.320.700.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.284.255 C18.452.284.255]

|

|

|-

| Lynch syndrome 1

| class of disease

| Lynch syndrome

| Lynch syndrome that has material basis in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16

| [http://www.disease-ontology.org/?id=DOID:0070271 DOID:0070271]

|

|

|

|-

| Lytico-bodig disease

| class of disease

| amyotrophic lateral sclerosis
progressive supranuclear palsy
neurodegenerative disease with dementia
neurodegeneration

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111246 DOID:0111246]

|

|

|

|-

| Léri–Weill dyschondrosteosis

| class of disease

| osteochondrodysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060847 DOID:0060847]

|

|

|

|-

| MALT lymphoma

| class of disease

| marginal zone B-cell lymphoma
primary cutaneous marginal zone lymphoma

| non-Hodgkin lymphoma that has material basis in mucosal tissue involved in antibody production

| [http://www.disease-ontology.org/?id=DOID:0050909 DOID:0050909]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386.480.150.570 C04.557.386.480.150.570]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.569.480.150.570 C15.604.515.569.480.150.570]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.761.480.150.570 C20.683.515.761.480.150.570]

|

|

|-

| MHC class I deficiency

| class of disease

| severe combined immunodeficiency
Bare lymphocyte syndrome

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060009 DOID:0060009]

|

|

|

|-

| MODY 1

| class of disease

| maturity-onset diabetes of the young

| medical condition

| [http://www.disease-ontology.org/?id=DOID:0111099 DOID:0111099]

|

|

|

|-

| MYH9-related disorder

| class of disease

| blood platelet disease
Inherited giant platelet disorder

| A blood platelet disease that has material basis in mutations in the MYH9 gene. It is characterized by thrombocytopenia, enlarged platelets, sensorineural hearing loss and presenile cataract.

| [http://www.disease-ontology.org/?id=DOID:0060651 DOID:0060651]

|

|

|

|-

| Maffucci syndrome

| class of disease

| syndrome
Ollier disease
disease

| syndrome characterized by the presence of multiple enchondromas (benign growths of cartilage) associated with multiple cavernous hemangiomas and phleboliths

| [http://www.disease-ontology.org/?id=DOID:0060221 DOID:0060221]

|

|

|

|-

| Mahvash Disease

| class of disease

| endocrine pancreas disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112306 DOID:0112306]

|

|

|

|-

| Martinez Monasterio Pinheiro syndrome

| class of disease

| cleft lip and cleft palate
hair diseases
syndactyly

| form of Blepharo-cheilo-dontic syndrome with with cleft lip and palate, complete absence of deciduous teeth, hypodontia of permanent teeth, hair alterations, hypertelorism, midface hypoplasia, abnormal EEG, syndactyly, and other findings

| [http://www.disease-ontology.org/?id=DOID:9003731 DOID:9003731]

|

|

|

|-

| Masters-Allen syndrome

| class of disease

| female reproductive system disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14133 DOID:14133]

|

|

|

|-

| Mayer-Rokitansky-Kuster-Hauser syndrome

| class of disease

| syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112177 DOID:0112177]

|

|

|

|-

| Mayer-Rokitansky-Kuster-Hauser syndrome type 1

| class of disease

|

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112178 DOID:0112178]

|

|

|

|-

| Meckel syndrome 1

| class of disease

| Meckel syndrome

| Meckel syndrome that has material basis in an autosomal recessive mutation of MKS1 on chromosome 17q22

| [http://www.disease-ontology.org/?id=DOID:0070115 DOID:0070115]

|

|

|

|-

| Meckel syndrome 13

| class of disease

| Meckel syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080253 DOID:0080253]

|

|

|

|-

| Meckel's diverticulitis

| class of disease

| diverticulitis

| diverticulits characterized by the inflammation of a congenital diverticulum, which is a slight bulge of the small intestine present at birth

| [http://www.disease-ontology.org/?id=DOID:8408 DOID:8408]

|

|

|

|-

| Meckel's diverticulum

| class of disease

| genetic disease
small intestine congenital defect
diverticulum
congenital disorder
disease

| congenital disorder of digestive system

| [http://www.disease-ontology.org/?id=DOID:9487 DOID:9487]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.198.859 C06.198.859]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.314.556 C16.131.314.556]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.300.415.750 C23.300.415.750]

| Meckel's diverticulum

| File:Diverticule de Meckel.jpg

|-

| Meckel's diverticulum cancer

| class of disease

| ileum cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10152 DOID:10152]

|

|

|

|-

| Meesmann corneal dystrophy 1

| class of disease

| Meesmann corneal dystrophy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080670 DOID:0080670]

|

|

|

|-

| Meesmann corneal dystrophy 2

| class of disease

| Meesmann corneal dystrophy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080671 DOID:0080671]

|

|

|

|-

| Meier-Gorlin syndrome 1

| class of disease

| Meier-Gorlin syndrome
autosomal recessive disease

| Meier-Gorlin syndrome that has material basis in homozygous or compound heterozygous mutation in the ORC1 gene on chromosome 1p32

| [http://www.disease-ontology.org/?id=DOID:0080512 DOID:0080512]

|

|

|

|-

| Meige syndrome

| class of disease

| cranio-facial dystonia
focal, segmental or multifocal dystonia

| cranio-facial dystonia that is accompanied by blepharospasm

| [http://www.disease-ontology.org/?id=DOID:3982 DOID:3982]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.079.590 C10.228.140.079.590]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.662.300.500 C10.228.662.300.500]

| Meige's syndrome

| File:DeGaper.png

|-

| Merkel cell carcinoma

| class of disease

| skin carcinoma
rare genetic developmental defect during embryogenesis
genetic epidermal disorder
skin tumor or hamartoma
inherited neuroendocrine tumor
genetic nervous system disorder
malignant dermis tumor
dermis disorder
neuroendocrine tumor with other location
nervous system cancer
rare nervous system tumor
disease

| rare and highly aggressive skin cancer

| [http://www.disease-ontology.org/?id=DOID:3965 DOID:3965]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C02.256.721.150 C02.256.721.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C02.928.216 C02.928.216]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.650.240.325 C04.557.465.625.650.240.325]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.370.325 C04.557.470.200.025.370.325]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.650.240.325 C04.557.580.625.650.240.325]

| Merkel cell carcinoma

| File:Merkel cell cancer.jpg

|-

| Middle East respiratory syndrome

| class of disease

| acute viral respiratory tract infection
coronavirus disease
disease

| viral respiratory infection in humans and camels

| [http://www.disease-ontology.org/?id=DOID:0080642 DOID:0080642]

|

| Middle East respiratory syndrome

| File:MERS-CoV electron micrograph3.jpg

|-

| Milker's nodule

| class of disease

| viral infectious disease
paravaccinia virus infection

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8729 DOID:8729]

|

|

|

|-

| Miller Fisher syndrome

| class of disease
symptom or sign

| Guillain–Barré syndrome
regional variant of Guillain-Barre syndrome

| Guillain-Barre syndrome that manifests as a descending paralysis

| [http://www.disease-ontology.org/?id=DOID:12889 DOID:12889]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.114.750.100.500 C10.114.750.100.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.252.500 C10.228.140.252.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.562.350 C10.292.562.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.314.750.450.500 C10.314.750.450.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.350.500 C10.668.829.350.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.800.750.300.500 C10.668.829.800.750.300.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.590.312 C11.590.312]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.258.750.400.500 C20.111.258.750.400.500]

|

|

|-

| Miller–Dieker lissencephaly syndrome

| class of disease
symptom or sign

| syndrome
autosomal dominant
classic lissencephaly
autosomal dominant disease
disease

| A syndrome characterized by classical lissencephaly and distinct facial features. Visible and submicroscopic deletions of 17p13.3, including the LIS1 gene, are found in almost 100% of patients.

| [http://www.disease-ontology.org/?id=DOID:0060469 DOID:0060469]

|

|

|

|-

| Mitis junctional epidermolysis bullosa

| class of disease

| junctional epidermolysis bullosa
genetic disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060738 DOID:0060738]

|

|

|

|-

| Miyoshi muscular dystrophy

| class of disease

| distal muscular dystrophy

| distal muscular dystrophy characterized by autosomal recessive inheritance of distal muscle weakness in the upper and lower limbs that spares the intrinsic muscles of the hands and has onset in young adulthood

| [http://www.disease-ontology.org/?id=DOID:0070198 DOID:0070198]

|

| Miyoshi myopathy

|

|-

| Miyoshi muscular dystrophy 1

| class of disease

| Miyoshi muscular dystrophy
genetic disease
autosomal recessive disease

| Miyoshi muscular dystrophy that has material basis in mutation in the DYSF gene on chromosome 2p13

| [http://www.disease-ontology.org/?id=DOID:0070199 DOID:0070199]

|

|

|

|-

| Miyoshi muscular dystrophy 2

| class of disease

| Miyoshi muscular dystrophy

| Miyoshi muscular dystrophy characterized by asymmetric presentation of muscle weakness and atrophy that has material basis in a locus on chromosome 10

| [http://www.disease-ontology.org/?id=DOID:0070200 DOID:0070200]

|

|

|

|-

| Monckeberg arteriosclerosis

| class of disease

| arteriosclerosis
vascular calcification

| Human's arterial pathology

| [http://www.disease-ontology.org/?id=DOID:5161 DOID:5161]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.174.130.780.500 C18.452.174.130.780.500]

| Monckeberg's arteriosclerosis

|

|-

| Mooren's ulcer

| class of disease

| corneal ulcer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10439 DOID:10439]

|

|

|

|-

| Morgagni cataract

| class of disease

| senile cataract

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13964 DOID:13964]

|

|

|

|-

| Mullegama-Klein-Martinez syndrome

| class of disease

| X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111845 DOID:0111845]

|

|

|

|-

| Mycoplasma pneumonia

| class of disease

| atypical pneumonia
bacterial pneumonia
Mycoplasma pneumoniae infection

| human disease

| [http://www.disease-ontology.org/?id=DOID:13276 DOID:13276]
[http://www.disease-ontology.org/?id=DOID:0050154 DOID:0050154]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.400.610.610.760 C01.150.252.400.610.610.760]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.620.500 C01.150.252.620.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.677.540.500 C08.381.677.540.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.730.610.540.545 C08.730.610.540.545]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.748.610.540.545 C01.748.610.540.545]

|

|

|-

| N,N'-diethylthiourea allergic contact dermatitis

| class of disease

| allergic contact dermatitis

| allergic contact dermatitis that has allergic trigger N,N-diethylthiourea

| [http://www.disease-ontology.org/?id=DOID:0040102 DOID:0040102]

|

|

|

|-

| N,N'-diphenylthiourea allergic contact dermatitis

| class of disease

| allergic contact dermatitis

| allergic contact dermatitis that has allergic trigger N,N-diphenylthiourea

| [http://www.disease-ontology.org/?id=DOID:0040101 DOID:0040101]

|

|

|

|-

| NK cell deficiency

| class of disease

| primary immunodeficiency disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080709 DOID:0080709]

|

|

|

|-

| NUT midline carcinoma

| class of disease

| carcinoma
rare tumor
undifferentiated carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060463 DOID:0060463]

|

| NUT midline carcinoma

|

|-

| Nezelof syndrome

| class of disease

| thymic hypoplasia
primary immunodeficiency disease
autosomal recessive disease
T cell deficiency

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2012 DOID:2012]

|

|

|

|-

| Niemann-Pick disease

| class of disease

| sphingolipidosis
disease

| severe metabolic disorders in which sphingomyelin accumulates in lysosomes in cells

| [http://www.disease-ontology.org/?id=DOID:14504 DOID:14504]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.163.100.435.825.700 C10.228.140.163.100.435.825.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.250.410.625 C15.604.250.410.625]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.189.435.825.700 C16.320.565.189.435.825.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.398.641.803.730 C16.320.565.398.641.803.730]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.595.554.825.700 C16.320.565.595.554.825.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.132.100.435.825.700 C18.452.132.100.435.825.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.687.803.730 C18.452.584.687.803.730]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.189.435.825.700 C18.452.648.189.435.825.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.398.641.803.730 C18.452.648.398.641.803.730]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.595.554.825.700 C18.452.648.595.554.825.700]

| Niemann–Pick disease

| File:Autorecessive-es.svg

|-

| Niemann-Pick disease type A

| class of disease

| Niemann-Pick disease
genetic disease

| A Niemann-Pick disease characterized by onset in infancy and involvement of neurological tissues that has material basis in an autosomal recessive mutation of SMPD1 on chromosome 11p15.4.

| [http://www.disease-ontology.org/?id=DOID:0070111 DOID:0070111]

|

|

|

|-

| Niemann-Pick disease type B

| class of disease

| Niemann-Pick disease
genetic disease

| a Niemann-Pick disease characterized by visceral involvement only and survival into adulthood: material basis in an autosomal recessive mutation of SMPD1 on chromosome 11p15.4

| [http://www.disease-ontology.org/?id=DOID:0070112 DOID:0070112]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.163.100.435.825.700.750 C10.228.140.163.100.435.825.700.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.250.410.625.750 C15.604.250.410.625.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.189.435.825.700.750 C16.320.565.189.435.825.700.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.398.641.803.730.750 C16.320.565.398.641.803.730.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.595.554.825.700.750 C16.320.565.595.554.825.700.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.132.100.435.825.700.750 C18.452.132.100.435.825.700.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.687.803.730.750 C18.452.584.687.803.730.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.189.435.825.700.750 C18.452.648.189.435.825.700.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.398.641.803.730.750 C18.452.648.398.641.803.730.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.595.554.825.700.750 C18.452.648.595.554.825.700.750]

|

|

|-

| Niemann-Pick disease, type C1

| class of disease

| Niemann-Pick disease
Niemann–Pick disease, type C
genetic disease

| Type C Niemann-Pick disease associated with a mutation in the gene NPC1, encoding Niemann-Pick C1 protein

| [http://www.disease-ontology.org/?id=DOID:0070113 DOID:0070113]

|

|

|

|-

| Niemann-Pick disease, type C2

| class of disease

| Niemann-Pick disease
Niemann–Pick disease, type C
genetic disease

| A Niemann-Pick disease that has material basis in an autosomal recessive mutation of NPC2 on chromosome 14q24.3.

| [http://www.disease-ontology.org/?id=DOID:0070114 DOID:0070114]

|

|

|

|-

| Nipah virus encephalitis

| class of disease

| viral encephalitis
Nipah virus infection
viral infectious disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050192 DOID:0050192]

|

|

|

|-

| Noonan syndrome 1

| class of disease

| Noonan syndrome

| A Noonan syndrome disease type 1 that has material basis in the PTPN11 gene on chromosome 12q24.

| [http://www.disease-ontology.org/?id=DOID:0060578 DOID:0060578]
[http://www.disease-ontology.org/?id=DOID:0070101 DOID:0070101]

|

|

|

|-

| Noonan syndrome 2

| class of disease

| Noonan syndrome
autosomal recessive disease

| Noonan syndrome that has material basis in an autosomal recessive mutation

| [http://www.disease-ontology.org/?id=DOID:0060580 DOID:0060580]
[http://www.disease-ontology.org/?id=DOID:0070102 DOID:0070102]

|

|

|

|-

| Noonan syndrome-like disorder with loose anagen hair 1

| class of disease

| Noonan syndrome-like disorder with loose anagen hair

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080692 DOID:0080692]

|

|

|

|-

| Noonan syndrome-like disorder with loose anagen hair 2

| class of disease

| Noonan syndrome-like disorder with loose anagen hair

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080693 DOID:0080693]

|

|

|

|-

| Ollier disease

| class of disease

| syndrome
enchondromatosis
disease

| rare nonhereditary sporadic disorder

| [http://www.disease-ontology.org/?id=DOID:4624 DOID:4624]

|

| Ollier disease

|

|-

| Opitz GBBB syndrome type I

| class of disease

| X-linked recessive disease
Opitz-GBBB syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080697 DOID:0080697]

|

|

|

|-

| Opitz GBBB syndrome type II

| class of disease

| Opitz-GBBB syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080698 DOID:0080698]

|

|

|

|-

| Oropouche fever

| class of disease

| viral infectious disease
Bunyaviridae infectious disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050521 DOID:0050521]

|

|

|

|-

| Orthomyxoviridae infectious disease

| class of disease

| (-)ssRNA virus infectious disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4493 DOID:4493]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.782.620 C01.925.782.620]

| Orthomyxoviridae infections

|

|-

| Osgood-Schlatter's disease

| class of disease

| bone inflammation disease
knee disorder
disease

| osteochondrosis

| [http://www.disease-ontology.org/?id=DOID:7489 DOID:7489]

|

| Osgood–Schlatter disease

| File:Osgood.jpg

|-

| Pacinian tumor

| class of disease

| neurofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2669 DOID:2669]

|

|

|

|-

| Paganini-Miozzo syndrome

| class of disease

| X-linked recessive disease
X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111843 DOID:0111843]

|

|

|

|-

| Pancoast tumor

| class of disease

| lung cancer
pulmonary sulcus neoplasm
disease

| tumor of the pulmonary apex

| [http://www.disease-ontology.org/?id=DOID:8007 DOID:8007]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.894.797.520.734 C04.588.894.797.520.734]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.540.734 C08.381.540.734]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.785.520.734 C08.785.520.734]

| Pancoast tumor

| File:Pancoast Tumor 1.jpg

|-

| Parkinson's disease 21

| class of disease

| autosomal dominant disease
hereditary late onset Parkinson disease

| late onset Parkinson's disease characterized by autosomal dominant inheritance and mean age of onset at 67 years

| [http://www.disease-ontology.org/?id=DOID:0111251 DOID:0111251]

|

|

|

|-

| Parkinson's disease 3

| class of disease

| Parkinson's disease

| late onset Parkinson's disease characterized by mean age of onset of 59 years and that has material basis in mutation in a locus in the 2p13 chromosome region

| [http://www.disease-ontology.org/?id=DOID:0111250 DOID:0111250]

|

|

|

|-

| Parry–Romberg syndrome

| class of disease

| facial nerve disease
brain inflammatory disease
inflammatory and autoimmune disease with epilepsy
genetic peripheral neuropathy
rare genetic epilepsy
disease

| a rare disease characterized by progressive shrinkage and degeneration of the tissues beneath the skin, usually on only one side of the face (hemifacial atrophy) but occasionally extending to other parts of the body

| [http://www.disease-ontology.org/?id=DOID:1757 DOID:1757]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.284 C07.465.284]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.299.375 C07.465.299.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.319.375 C10.292.319.375]

| Parry–Romberg syndrome

| File:Parry Romberg Syndrome 1.jpg

|-

| Partington X-linked mental retardation syndrome

| class of disease

| X-linked intellectual disability
X-linked recessive disease

| syndrome characterized by intellectual disability, focal dystonia of the hands and dysarthria

| [http://www.disease-ontology.org/?id=DOID:14744 DOID:14744]

|

|

|

|-

| Patau syndrome

| class of disease

| chromosomal disease
total autosomal trisomy
trisomy 13
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11665 DOID:11665]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.606.360.835 C10.597.606.360.835]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.240.400.970 C14.240.400.970]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.400.970 C14.280.400.970]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.240.400.965 C16.131.240.400.965]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.180.923 C16.320.180.923]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.260.923 C16.131.260.923]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.077.919 C16.131.077.919]

| Patau syndrome

| File:Chromosome 13.jpeg

|-

| Pearson syndrome

| class of disease

| mitochondrial disease

| mitochondrial metabolism disease

| [http://www.disease-ontology.org/?id=DOID:0060067 DOID:0060067]

|

|

|

|-

| Perrault syndrome 6

| class of disease

| Perrault syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080256 DOID:0080256]

|

|

|

|-

| Peyronie's disease

| class of disease

| penile disease
fibromatosis
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8616 DOID:8616]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.494.508 C12.294.494.508]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.715 C17.300.715]

| Peyronie's disease

| File:Peyronie disease.jpg

|-

| Phlegmonous dacryocystitis

| class of disease

| dacryocystitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12997 DOID:12997]

|

|

|

|-

| Plasmodium ovale malaria

| class of disease

| malaria

| malaria characaterized as a relatively mild form caused by a parasite Plasmodium ovale, which is characterized by tertian chills and febrile paroxysms, and that ends spontaneously

| [http://www.disease-ontology.org/?id=DOID:12919 DOID:12919]

|

|

|

|-

| Pleomorphic xanthoastrocytoma

| class of disease

| astrocytoma
low-grade astrocytoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4852 DOID:4852]

|

| Pleomorphic xanthoastrocytoma

|

|-

| Plummer's disease

| class of disease

| hyperthyroidism
nodular goiter

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11277 DOID:11277]

|

|

|

|-

| Posner-Schlossman Syndrome

| class of disease

| iridocyclitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9378 DOID:9378]

|

|

|

|-

| Potter's syndrome

| class of disease

| sequence
renal agenesis
disease

| congenital disorder of urinary system

| [http://www.disease-ontology.org/?id=DOID:12594 DOID:12594]

|

|

|

|-

| Prieto syndrome

| class of disease

| X-linked intellectual disability
X-linked recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060805 DOID:0060805]

|

|

|

|-

| Prinzmetal's angina

| class of disease

| Vangina pectoris
coronaropathy
coronary artery vasospasm
disease

| cardiac chest pain at rest that occurs in cycles

| [http://www.disease-ontology.org/?id=DOID:0111151 DOID:0111151]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.647.187.150.150 C14.280.647.187.150.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.585.187.150.500 C14.907.585.187.150.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.612.233.500.150.150 C23.888.592.612.233.500.150.150]

|

|

|-

| Pthirus pubis infestation

| class of disease

| ectoparasitism
lice infestation

| disease caused by the pubic louse, Pthirus pubis, a parasitic insect notorious for infesting human pubic hair

| [http://www.disease-ontology.org/?id=DOID:13760 DOID:13760]

|

| Pubic lice

| File:SOA-Pediculosis-pubis.jpg

|-

| Qazi Markouizos syndrome

| class of disease

| syndrome
genetic syndromic intellectual disability

| syndrome that is characterized by hypotonia, congenital fiber type disproportion and dysharmonic skeletal maturation

| [http://www.disease-ontology.org/?id=DOID:0050740 DOID:0050740]

|

|

|

|-

| Quartan fever

| class of disease

| malaria

| malaria caused by a parasite Plasmodium malariae, which is marked by recurrence of paroxysms at 72-hour intervals

| [http://www.disease-ontology.org/?id=DOID:14324 DOID:14324]

|

|

|

|-

| RASopathy

| class of disease

| genetic disease
syndrome

| Family of genetic conditions caused by mutations affecting Ras genes

| [http://www.disease-ontology.org/?id=DOID:0080690 DOID:0080690]

|

|

|

|-

| REM sleep behavior disorder

| class of disease

| sleep disorder

| sleep disorder that involves abnormal behavior including the acting out of violent or dramatic dreams during the sleep phase with rapid eye movement

| [http://www.disease-ontology.org/?id=DOID:9091 DOID:9091]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.886.659.633.700 C10.886.659.633.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.870.664.633.700 F03.870.664.633.700]

|

|

|-

| RNASET2-deficient cystic leukoencephalopathy

| class of disease

| autosomal recessive disease
leukodystrophy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0081007 DOID:0081007]

|

|

|

|-

| Raynaud disease

| class of disease

| peripheral vascular disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10300 DOID:10300]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.617.812 C14.907.617.812]

| Raynaud's disease

|

|-

| Raynaud-Claes syndrome

| class of disease

| X-linked dominant disease
X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112060 DOID:0112060]

|

|

|

|-

| Reye syndrome

| class of disease

| syndrome
encephalopathy
systemic disease
disease

| syndrome characterized by acute brain damage and liver function problems

| [http://www.disease-ontology.org/?id=DOID:14525 DOID:14525]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.241.649 C06.552.241.649]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.163.780 C10.228.140.163.780]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.132.780 C18.452.132.780]

| Reye's syndrome

| File:Reye's syndrome liver-histology.jpg

|-

| Rh disease

| class of disease

| fetal erythroblastosis
blood group incompatibility

| problem with Rh+ fetuses in Rh- mothers

| [http://www.disease-ontology.org/?id=DOID:4175 DOID:4175]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=G09.188.114.750 G09.188.114.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=G12.122.780 G12.122.780]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=G12.186.750 G12.186.750]

|

|

|-

| Richter's syndrome

| class of disease

| chronic lymphocytic leukemia
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1703 DOID:1703]

|

|

|

|-

| Rickettsia parkeri spotted fever

| class of disease

| spotted fever

| A spotted fever that has material basis in Rickettsia parkeri, which is transmitted by Gulf Coast tick (Amblyomma maculatum). The infection has symptom fever, has symptom headache, has symptom eschar, and has symptom rash.

| [http://www.disease-ontology.org/?id=DOID:0050051 DOID:0050051]

|

|

|

|-

| Riedel's fibrosing thyroiditis

| class of disease

| thyroiditis
disease

| thyroid disease

| [http://www.disease-ontology.org/?id=DOID:14351 DOID:14351]

|

|

|

|-

| Riley-Day syndrome

| class of disease

| hereditary sensory and autonomic neuropathy
primary orthostatic hypotension
rare genetic developmental defect during embryogenesis
other dermis disorder
other genetic dermis disorder
nervous system anomaly with eye involvement
autosomal recessive hereditary sensory and autonomic neuropathy
disease

| hereditary sensory and autonomic neuropathy type III (HSAN-III), is a disorder of the autonomic nervous system which affects the development and survival of sensory

| [http://www.disease-ontology.org/?id=DOID:11589 DOID:11589]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.177.575.300 C10.177.575.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.500.310.309 C10.500.310.309]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.500.496.250 C10.574.500.496.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.800.175.250 C10.668.829.800.175.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.666.310.309 C16.131.666.310.309]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.400.415.309 C16.320.400.415.309]

| Familial dysautonomia

| File:Riley day.jpg

|-

| Ritscher-Schinzel syndrome 1

| class of disease

| Ritscher–Schinzel syndrome
genetic disease

| Ritscher-Schinzel syndrome that has material basis in homozygous mutation in the KIAA0196 gene on chromosome 8q24

| [http://www.disease-ontology.org/?id=DOID:0060571 DOID:0060571]

|

|

|

|-

| Ritter's disease

| class of disease

| staphylococcal infection
commensal bacterial infectious disease
skin disease
perinatal infectious disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9063 DOID:9063]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.410.868.951.770 C01.150.252.410.868.951.770]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.819.770.770 C01.150.252.819.770.770]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.800.720.770.770 C01.800.720.770.770]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.838.765.770.770 C17.800.838.765.770.770]

| Staphylococcal scalded skin syndrome

| File:OSC Microbio 21 02 SSSS.jpg

|-

| SAPHO syndrome

| class of disease

| syndrome
autoinflammatory syndrome with skin involvement
pyogenic autoinflammatory syndrome
disease

| variety of inflammatory bone disorders that may be associated with skin changes

| [http://www.disease-ontology.org/?id=DOID:13677 DOID:13677]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.099.708.025 C05.116.099.708.025]

|

| File:Hiperostosis EC.JPG

|-

| SM-AHNMD

| class of disease

| systemic mastocytosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4797 DOID:4797]

|

|

|

|-

| SOST-related sclerosing bone dysplasia

| class of disease

| hyperostosis
genetic disease
autosomal recessive disease

| hyperostosis that has material basis in a mutation in the SOST gene which results in overgrowth of endosteal bone producing dense and wide bones throughout the body especially located in skull

| [http://www.disease-ontology.org/?id=DOID:0080036 DOID:0080036]

|

|

|

|-

| Sabinas brittle hair syndrome

| class of disease

| trichothiodystrophy syndromes
genetic disease
nonphotosensitive trichothiodystrophy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111874 DOID:0111874]

|

|

|

|-

| Sakati-Nyhan syndrome

| class of disease

| acrocephalosyndactylia

| An acrocephalosyndactylia characterized by abnormalities in the bones of the legs, congenital heart defects and craniofacial defects and craniosynostosis. The patients suffer from cyanosis and other respiratory and breathing infections.

| [http://www.disease-ontology.org/?id=DOID:0060359 DOID:0060359]

|

|

|

|-

| Sarcomatoid carcinoma of the lung

| class of disease

| large-cell lung carcinoma
Sarcomatoid carcinoma
lung carcinoma

| medical condition

| [http://www.disease-ontology.org/?id=DOID:0080777 DOID:0080777]

|

| Sarcomatoid carcinoma of lung

|

|-

| Scheuermann's disease

| class of disease

| osteochondrosis
kyphosis
spinal osteochondrosis
osteochondrosis of genetic origin
spinal disease
disease

| osteochondrosis that results in abnormal bone growth and curvature located in thoracic vertebral column

| [http://www.disease-ontology.org/?id=DOID:13300 DOID:13300]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.821.500.500 C05.116.821.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.900.800.500.500 C05.116.900.800.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.900.808.500 C05.116.900.808.500]

| Scheuermann's disease

| File:Scheuermanns diseasebl.jpg

|-

| Schnitzler syndrome

| class of disease

| type IV hypersensitivity
autoimmune urticaria
unexplained periodic fever syndrome
chronic urticaria

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4371 DOID:4371]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.780.640.700 C20.683.780.640.700]

|

|

|-

| Schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma

| class of disease

| nodular ganglioneuroblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7951 DOID:7951]

|

|

|

|-

| Seckel syndrome 1

| class of disease

| Seckel syndrome

| Seckel syndrome that has material basis in homozygous or compound heterozygous mutation in the ATR gene on chromosome 3q23

| [http://www.disease-ontology.org/?id=DOID:0070007 DOID:0070007]

|

|

|

|-

| Sertoli cell tumor

| class of disease

| testicular sex cord-stromal neoplasm
sex cord-gonadal stromal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3577 DOID:3577]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.475.750.847.500 C04.557.475.750.847.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.762.500.500 C04.588.322.762.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.945.440.915.500.500 C04.588.945.440.915.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.260.937.500.500 C12.294.260.937.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.758.409.937.500.500 C12.758.409.937.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.762.500.500 C19.344.762.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.829.782.500.500 C19.391.829.782.500.500]

| Sertoli cell tumor

|

|-

| Sertoli-Leydig cell tumor

| class of disease

| testicular sex cord-stromal neoplasm
sex cord-gonadal stromal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2997 DOID:2997]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.475.750.847 C04.557.475.750.847]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.455.648 C04.588.322.455.648]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.762.500 C04.588.322.762.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.945.440.915.500 C04.588.945.440.915.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.260.937.500 C12.294.260.937.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.758.409.937.500 C12.758.409.937.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.056.630.705.648 C13.351.500.056.630.705.648]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.937.418.685.648 C13.351.937.418.685.648]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.410.648 C19.344.410.648]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.762.500 C19.344.762.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.630.705.648 C19.391.630.705.648]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.829.782.500 C19.391.829.782.500]

|

|

|-

| Sezary's disease

| class of disease

| cutaneous T cell lymphoma
aggressive primary cutaneous T-cell lymphoma
disease

| type of cutaneous lymphoma

| [http://www.disease-ontology.org/?id=DOID:8541 DOID:8541]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386.480.750.800.775 C04.557.386.480.750.800.775]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.569.480.750.800.775 C15.604.515.569.480.750.800.775]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.841 C15.604.515.841]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.761.480.750.800.775 C20.683.515.761.480.750.800.775]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.920 C20.683.515.920]

| Sézary's disease

| File:Sézary's disease.jpg

|-

| Sheehan's syndrome

| class of disease

| puerperal disorders
necrosis of pituitary
Simmonds' cachexia
hypopituitarism
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:9476 DOID:9476]

|

|

|

|-

| Shukla-Vernon syndrome

| class of disease

| X-linked recessive disease
syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111841 DOID:0111841]

|

|

|

|-

| Shwartzman phenomenon

| class of disease

| vasculitis
vascular hemostatic disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3825 DOID:3825]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.454.810 C14.907.454.810]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.940.890 C14.907.940.890]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463.515.810 C15.378.463.515.810]

|

|

|-

| Simpson-Golabi-Behmel syndrome type 2

| class of disease

| X-linked recessive disease
Simpson-Golabi-Behmel syndrome

| X-linked recessive disease that has material basis in mutation in the OFD1 gene on chromosome Xp22 and is characterized by developmental delay, macrocephaly, and respiratory problems

| [http://www.disease-ontology.org/?id=DOID:0080342 DOID:0080342]

|

|

|

|-

| Skene gland carcinoma

| class of disease

| paraurethral gland cancer
carcinoma
vulva adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7284 DOID:7284]

|

|

|

|-

| Smarca4-deficient sarcoma of thorax

| class of disease

| thoracic cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080532 DOID:0080532]

|

|

|

|-

| Sotos syndrome 1

| class of disease

| autosomal dominant disease
Sotos syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112103 DOID:0112103]

|

|

|

|-

| Sotos syndrome 2

| class of disease

| Sotos syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112102 DOID:0112102]

|

|

|

|-

| Spinal cord cancer

| class of disease

| central nervous system cancer
spinal cord disease
spinal cord neoplasm

| central nervous system cancer that is located in the spinal cord

| [http://www.disease-ontology.org/?id=DOID:5612 DOID:5612]

|

|

|

|-

| Spirurida infectious disease

| class of disease

| filariasis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1077 DOID:1077]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.610.335.508.700.750 C01.610.335.508.700.750]

|

|

|-

| Stickler syndrome 1

| class of disease

| Stickler syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080676 DOID:0080676]

|

|

|

|-

| Stickler syndrome type 2

| class of disease

| Stickler syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080675 DOID:0080675]

|

|

|

|-

| Sudeck's syndrome

| class of disease

| complex regional pain syndrome
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1811 DOID:1811]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.177.195.800 C10.177.195.800]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.250.800 C10.668.829.250.800]

|

|

|-

| Sugarman brachydactyly

| class of disease

| brachydactyly

| brachydactyly characterized by a nonarticulating great toe set dorsal and proximal to the typical position

| [http://www.disease-ontology.org/?id=DOID:0110979 DOID:0110979]

|

|

|

|-

| Sweeney-Cox syndrome

| class of disease

| syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080538 DOID:0080538]

|

|

|

|-

| T cell and NK cell immunodeficiency

| class of disease

| primary immunodeficiency disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080710 DOID:0080710]

|

|

|

|-

| T cell deficiency

| class of disease

| primary immunodeficiency disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11200 DOID:11200]
[http://www.disease-ontology.org/?id=DOID:613 DOID:613]

|

|

| File:Healthy Human T Cell.jpg

|-

| T cell, B cell, and NK cell deficiency

| class of disease

| combined immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111965 DOID:0111965]

|

|

|

|-

| T-cell acute lymphoblastic leukemia

| class of disease

| acute T cell leukemia
lymphoma
acute lymphocytic leukemia
viral infectious disease
T-cell leukemia

| Acute lymphoblastic leukemia of T-cell origin. It comprises about 15% of childhood cases and 25% of adult cases. It is more common in males than females. (WHO, 2001)

| [http://www.disease-ontology.org/?id=DOID:5603 DOID:5603]
[http://www.disease-ontology.org/?id=DOID:0050523 DOID:0050523]

|

|

|

|-

| T-cell adult acute lymphocytic leukemia

| class of disease

| adult acute lymphocytic leukemia
T-cell leukemia
T-cell acute lymphoblastic leukemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5602 DOID:5602]

|

|

|

|-

| T-cell childhood acute lymphocytic leukemia

| class of disease

| childhood acute lymphocytic leukemia
T-cell acute lymphoblastic leukemia

| childhood acute lymphoblastic leukemia that has material basis in T-cells

| [http://www.disease-ontology.org/?id=DOID:0080145 DOID:0080145]

|

|

|

|-

| T-cell childhood lymphoblastic lymphoma

| class of disease

| lymphoblastic lymphoma
Precursor T-lymphoblastic lymphoma

| lymphoblastic lymphoma that has material basis in T-cells and that occurs during childhood

| [http://www.disease-ontology.org/?id=DOID:0080148 DOID:0080148]

|

|

|

|-

| T-cell large granular lymphocyte leukemia

| class of disease

| chronic lymphocytic leukemia
acquired neutropenia
T-cell leukemia
disease

| chronic lymphocytic leukemia that exhibits an unexplained, chronic (> 6 months) elevation in large granular lymphocytes (LGLs) in the peripheral blood

| [http://www.disease-ontology.org/?id=DOID:0050751 DOID:0050751]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.428.580.049 C04.557.337.428.580.049]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.560.575.049 C15.604.515.560.575.049]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.528.582.049 C20.683.515.528.582.049]

|

|

|-

| T-cell leukemia

| class of disease

| leukocyte disease
lymphoblastic leukemia
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:715 DOID:715]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.428.580 C04.557.337.428.580]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.560.575 C15.604.515.560.575]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.528.582 C20.683.515.528.582]

|

|

|-

| Taylor's syndrome

| class of disease

| uterine disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9346 DOID:9346]

|

| Pelvic congestion syndrome

|

|-

| Teebi hypertelorism syndrome 2

| class of disease

| Hypertelorism, Teebi type

| human disease

| [http://www.disease-ontology.org/?id=DOID:0081074 DOID:0081074]

|

|

|

|-

| Timothy grass allergy

| class of disease

| pollen allergy

| pollen allergy triggered by Phleum pratense pollen

| [http://www.disease-ontology.org/?id=DOID:0060498 DOID:0060498]

|

|

|

|-

| Tn Polyagglutination syndrome

| class of disease

| genetic disease
hematopoietic system disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080520 DOID:0080520]

|

|

|

|-

| Treacher Collins syndrome 1

| class of disease

| Treacher Collins syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080789 DOID:0080789]

|

|

|

|-

| Treacher Collins syndrome 2

| class of disease

| Treacher Collins syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080790 DOID:0080790]

|

|

|

|-

| Treacher Collins syndrome 3

| class of disease

| Treacher Collins syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080791 DOID:0080791]

|

|

|

|-

| Treacher Collins syndrome 4

| class of disease

| Treacher Collins syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080792 DOID:0080792]

|

|

|

|-

| Trichohepatoenteric syndrome 2

| class of disease

| tricho-hepato-enteric syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111416 DOID:0111416]

|

|

|

|-

| Turner syndrome

| class of disease

| gonadal dysgenesis
X chromosome number anomaly with female phenotype
disease

| chromosomal disorder in which a female is partially or completely missing an X chromosome

| [http://www.disease-ontology.org/?id=DOID:3491 DOID:3491]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.875.253.309.872 C12.050.351.875.253.309.872]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.875.253.795.750 C12.050.351.875.253.795.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.706.316.309.872 C12.200.706.316.309.872]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.706.316.795.750 C12.200.706.316.795.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.240.400.980 C14.240.400.980]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.400.980 C14.280.400.980]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.240.400.970 C16.131.240.400.970]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.260.830.835.750 C16.131.260.830.835.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.316.309.872 C16.131.939.316.309.872]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.316.795.750 C16.131.939.316.795.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.180.830.835.750 C16.320.180.830.835.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.119.309.872 C19.391.119.309.872]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.119.795.750 C19.391.119.795.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.800.316.309.872 C12.800.316.309.872]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.800.316.795.750 C12.800.316.795.750]

| Turner syndrome

| File:45,X.jpg

|-

| Uruguay faciocardiomusculoskeletal syndrome

| class of disease

| genetic disease
syndrome
cardiomyopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112148 DOID:0112148]

|

|

|

|-

| Usher syndrome type 1

| class of disease

| Usher syndrome

| Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa

| [http://www.disease-ontology.org/?id=DOID:0110826 DOID:0110826]

|

|

|

|-

| Usher syndrome type 1E

| class of disease

| Usher syndrome type 1

| Usher syndrome type 1 that has material basis in variation in the chromosome region 21q21

| [http://www.disease-ontology.org/?id=DOID:0110833 DOID:0110833]

|

|

|

|-

| Usher syndrome type 1H

| class of disease

| Usher syndrome type 1

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110835 DOID:0110835]

|

|

|

|-

| Usher syndrome type 1K

| class of disease

| Usher syndrome type 1

| An Usher syndrome type 1 that has material basis in variation in the chromosome region 10p11.21-q21.1.

| [http://www.disease-ontology.org/?id=DOID:0110837 DOID:0110837]

|

|

|

|-

| Usher syndrome type 2

| class of disease

| Usher syndrome

| Usher syndrome characterized by mild to severe congenital hearing impairment, normal vestibular function and later development of retinitis pigmentosa

| [http://www.disease-ontology.org/?id=DOID:0110827 DOID:0110827]

|

|

|

|-

| Usher syndrome type 3

| class of disease

| Usher syndrome

| Usher syndrome characterized by progressive hearing loss typically beginning in late childhood, variable vestibular dysfunction and onset of retinitis pigmentosa by the second decade of life

| [http://www.disease-ontology.org/?id=DOID:0110828 DOID:0110828]

|

|

|

|-

| VIPoma

| class of disease

| neuroendocrine tumor

| rare endocrine tumor that overproduces vasoactive intestinal peptide

| [http://www.disease-ontology.org/?id=DOID:5574 DOID:5574]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.650.240.847 C04.557.465.625.650.240.847]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.370.847 C04.557.470.200.025.370.847]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.761.500.750 C04.588.274.761.500.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.475.500.750 C04.588.322.475.500.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.761.500.750 C06.301.761.500.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.689.667.500.750 C06.689.667.500.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.421.500.750 C19.344.421.500.750]

|

|

|-

| Van Esch-O'Driscoll syndrome

| class of disease

| X-linked recessive disease
X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111840 DOID:0111840]

|

|

|

|-

| Van Maldergem syndrome 1

| class of disease

| Van Maldergem syndrome

| Van Maldergem syndrome that has material basis in homozygous mutation in the DCHS1 gene on chromosome 11p15

| [http://www.disease-ontology.org/?id=DOID:0080585 DOID:0080585]

|

|

|

|-

| Van Maldergem syndrome 2

| class of disease

| Van Maldergem syndrome

| Van Malergem syndrome that has material basis in homozygous or compound heterozygous mutation in the FAT4 gene on chromosome 4q28

| [http://www.disease-ontology.org/?id=DOID:0080586 DOID:0080586]

|

|

|

|-

| Verruciform xanthoma

| class of disease

| xanthomatosis
skin disease
xanthoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5769 DOID:5769]

|

|

|

|-

| Volkmann's contracture

| class of disease

| connective tissue disease
disease

| permanent flexion contracture of the hand at the wrist, resulting in a claw-like deformity of the hand and fingers

| [http://www.disease-ontology.org/?id=DOID:5587 DOID:5587]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.550.323.734 C05.550.323.734]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.180.531 C05.651.180.531]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.197.734 C05.651.197.734]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.303.531 C14.907.303.531]

| Volkmann's contracture

| File:The practice of surgery (1910) (14756898256).jpg

|-

| WNT4 deficiency

| class of disease

| partial bilateral aplasia of the mullerian ducts
sex differentiation disease
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111526 DOID:0111526]

|

|

|

|-

| Waardenburg syndrome type 1

| class of disease

| Waardenburg's syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110948 DOID:0110948]

|

|

|

|-

| Waardenburg syndrome type 2B

| class of disease

| Waardenburg's syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110947 DOID:0110947]

|

|

|

|-

| Waardenburg syndrome type 2C

| class of disease

| Waardenburg's syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110951 DOID:0110951]

|

|

|

|-

| Waldenström macroglobulinemia

| class of disease

| B-cell lymphoma
lymphoplasmacytic lymphoma
disease

| Type of blood cancer

| [http://www.disease-ontology.org/?id=DOID:0060901 DOID:0060901]
[http://www.disease-ontology.org/?id=DOID:0050747 DOID:0050747]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.595.925 C04.557.595.925]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.454.960 C14.907.454.960]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.147.780.925 C15.378.147.780.925]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463.515.960 C15.378.463.515.960]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.925 C15.604.515.925]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.780.925 C20.683.780.925]

|

|

|-

| Warburg micro syndrome 1

| class of disease

| Warburg micro syndrome

| Warburg micro syndrome that has material basis in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP1 gene on chromosome 2q21

| [http://www.disease-ontology.org/?id=DOID:0110716 DOID:0110716]

|

|

|

|-

| Waterhouse-Friderichsen syndrome

| class of disease

| adrenal crisis
adrenal gland disease
disease

| adrenal gland disease that is characterized by failure of the adrenal gland due to bleeding into the gland

| [http://www.disease-ontology.org/?id=DOID:9931 DOID:9931]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.223.500.750.500 C01.150.252.223.500.750.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.400.625.549.449.800 C01.150.252.400.625.549.449.800]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.228.180.500.750.500 C10.228.228.180.500.750.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.586.625.280.505.904 C10.586.625.280.505.904]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100.802.843 C15.378.100.802.843]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463.950 C15.378.463.950]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.053.500.740 C19.053.500.740]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.414.950.843 C23.550.414.950.843]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.885.687.843 C23.888.885.687.843]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.207.180.500.750.500 C01.207.180.500.750.500]

| Waterhouse–Friderichsen syndrome

| File:Waterhouse-Friderichsen. IMG 2912.jpg

|-

| Weissenbacher-Zweymuller syndrome

| class of disease

| Pierre Robin syndrome
osteochondrodysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:4258 DOID:4258]

|

|

|

|-

| Wernicke encephalopathy

| class of disease

| encephalopathy
long-term effects of alcohol consumption
thiamine deficiency
disease

| presence of neurological symptoms caused by biochemical lesions of the central nervous system after exhaustion of B-vitamin reserves,

| [http://www.disease-ontology.org/?id=DOID:2384 DOID:2384]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.163.960 C10.228.140.163.960]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.132.960 C18.452.132.960]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.654.521.500.133.699.827.822 C18.654.521.500.133.699.827.822]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.775.100.625 C25.775.100.625]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.900.100.875 F03.900.100.875]

|

|

|-

| Whitewater Arroyo hemorrhagic fever

| class of disease

| viral infectious disease
viral hemorrhagic fever

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050199 DOID:0050199]

|

|

|

|-

| Wolf-Hirschhorn syndrome

| class of disease

| chromosomal deletion syndrome
partial deletion of the short arm of chromosome 4
disease

| chromosome abnormality with a distinct craniofacial phenotype and intellectual disability

| [http://www.disease-ontology.org/?id=DOID:0050460 DOID:0050460]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.077.944 C16.131.077.944]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.260.985 C16.131.260.985]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.180.985 C16.320.180.985]

| Wolf–Hirschhorn syndrome

| File:Mia - whs.jpg

|-

| Wolffian adnexal neoplasm

| class of disease

| uterine ligament cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7514 DOID:7514]

|

|

|

|-

| Wolffian duct adenocarcinoma

| class of disease

| cervical adenocarcinoma
mesonephric tumor
clear cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5368 DOID:5368]

|

|

|

|-

| Wolffian duct adenoma

| class of disease

| reproductive organ benign neoplasm
benign neoplasms by histologic type
benign mesonephroma
adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2616 DOID:2616]

|

|

|

|-

| Wolfram syndrome 1

| class of disease

| Wolfram syndrome
autosomal recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0110629 DOID:0110629]

|

|

|

|-

| Wolfram syndrome 2

| class of disease

| Wolfram syndrome
autosomal recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0110630 DOID:0110630]

|

|

|

|-

| Wolfram syndrome, mitochondrial form

| class of disease

| Wolfram syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080583 DOID:0080583]

|

|

|

|-

| Wolman disease

| class of disease

| lysosomal and lipase deficiency

| autosomal recessive inborn error of metabolism that results in the body not producing enough active lysosomal acid lipase (LAL) enzyme

| [http://www.disease-ontology.org/?id=DOID:14497 DOID:14497]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.398.641.201.500 C16.320.565.398.641.201.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.595.201.500 C16.320.565.595.201.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.614.947 C16.614.947]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.563.641.201.500 C18.452.584.563.641.201.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.398.641.201.500 C18.452.648.398.641.201.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.595.201.500 C18.452.648.595.201.500]

| Lysosomal acid lipase deficiency

|

|-

| X-Linked immunodeficiency 74

| class of disease

| X-linked recessive disease
T cell deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112063 DOID:0112063]

|

|

|

|-

| X-linked Emery-Dreifuss muscular dystrophy 1

| class of disease

| Emery-Dreifuss muscular dystrophy
X-linked recessive disease

| Emery-Dreifuss muscular dystrophy that has material basis in an X-linked recessive mutation of EMD on chromosome Xq28

| [http://www.disease-ontology.org/?id=DOID:0070246 DOID:0070246]

|

|

|

|-

| X-linked Emery-Dreifuss muscular dystrophy 6

| class of disease

| Emery-Dreifuss muscular dystrophy
X-linked recessive disease

| An Emery-Dreifuss muscular dystrophy that has material basis in an X-linked recessive mutation of FHL1 on chromosome Xq26.3.

| [http://www.disease-ontology.org/?id=DOID:0070251 DOID:0070251]

|

|

|

|-

| X-linked agammaglobulinemia type 2

| class of disease

| Bruton-type agammaglobulinemia
autosomal recessive disease
B cell deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111999 DOID:0111999]

|

|

|

|-

| X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2

| class of disease

| amelogenesis imperfecta

| amelogenesis imperfecta associated with mutation in a gene in the Xq22-q28 region

| [http://www.disease-ontology.org/?id=DOID:0110059 DOID:0110059]

|

|

|

|-

| X-linked cardiac valvular dysplasia

| class of disease

| X-linked disease
heart valve disease
Heart valve dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111765 DOID:0111765]

|

|

|

|-

| X-linked chondrodysplasia punctata

| class of disease

| chondrodysplasia punctata
X-linked recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060292 DOID:0060292]

|

|

|

|-

| X-linked chondrodysplasia punctata 2

| class of disease

| X-linked dominant disease
chondrodysplasia punctata

| chondrodysplasia puncata that has material basis in mutation in the gene encoding delta(8)-delta(7) sterol isomerase emopamil-binding protein on chromosome Xp11

| [http://www.disease-ontology.org/?id=DOID:0080352 DOID:0080352]

|

|

|

|-

| X-linked chronic granulomatous disease

| class of disease

| X-linked recessive disease
chronic granulomatous disease

| A chronic granulomatous disease characterized by X-linked inheritance that has material basis in mutation in the CYBB gene on chromosome Xp21.1-p11.4.

| [http://www.disease-ontology.org/?id=DOID:0070195 DOID:0070195]

|

|

|

|-

| X-linked chronic idiopathic intestinal pseudo-obstruction

| class of disease

| X-linked recessive disease
neuronal intestinal dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080681 DOID:0080681]

|

|

|

|-

| X-linked cone-rod dystrophy 2

| class of disease

| cone-rod dystrophy

| cone-rod dystrophy that has material basis in variation in the chromosome region Xq27

| [http://www.disease-ontology.org/?id=DOID:0111006 DOID:0111006]

|

|

|

|-

| X-linked congenital hemolytic anemia

| class of disease

| congenital hemolytic anemia
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111846 DOID:0111846]

|

|

|

|-

| X-linked congenital myopathy with fiber-type disproportion

| class of disease

| congenital fiber-type disproportion

| A congenital fiber-type disproportion characterized by bilateral ptosis, facial weakness, impaired suckling, generalized hypotonia, and respiratory insufficiency that has material basis in mutation in the chromosome region Xq13.1-q22.1.

| [http://www.disease-ontology.org/?id=DOID:0111226 DOID:0111226]

|

|

|

|-

| X-linked deafness 1

| class of disease

| X-linked nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111739 DOID:0111739]

|

|

|

|-

| X-linked deafness 2

| class of disease

| X-linked nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111737 DOID:0111737]

|

|

|

|-

| X-linked deafness 3

| class of disease

| X-linked nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111736 DOID:0111736]

|

|

|

|-

| X-linked deafness 7

| class of disease

| X-linked nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111738 DOID:0111738]

|

|

|

|-

| X-linked disease

| class of disease

| monogenic disease

| monogenic disease that has material basis in mutations in genes on the X chromosome

| [http://www.disease-ontology.org/?id=DOID:0050735 DOID:0050735]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.322 C16.320.322]

|

|

|-

| X-linked dyskeratosis congenita

| class of disease

| dyskeratosis congenita
X-linked recessive disease

| dyskeratosis congenita that has material basis in an X-linked recessive mutation of DKC1 on chromosome Xq28

| [http://www.disease-ontology.org/?id=DOID:0070025 DOID:0070025]

|

|

|

|-

| X-linked endothelial corneal dystrophy

| class of disease

| corneal endothelial dystrophy
posterior corneal dystrophy
X-linked dominant disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060446 DOID:0060446]

|

|

|

|-

| X-linked exudative vitreoretinopathy 2

| class of disease

| X-linked disease
exudative vitreoretinopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111413 DOID:0111413]

|

|

|

|-

| X-linked hyper IgM syndrome

| class of disease

| hyperimmunoglobulin syndrome
hyper IgM syndrome
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:6620 DOID:6620]

|

|

|

|-

| X-linked intellectual developmental disorder 108

| class of disease

| X-linked recessive disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111844 DOID:0111844]

|

|

|

|-

| X-linked keratosis follicularis spinulosa decalvans

| class of disease

| keratosis follicularis spinulosa decalvans
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080754 DOID:0080754]

|

|

|

|-

| X-linked lymphoproliferative syndrome 2

| class of disease

| lymphoproliferative disorders
X-linked lymphoproliferative disease
X-linked recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060706 DOID:0060706]

|

|

|

|-

| X-linked mental retardation 106

| class of disease

| non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080240 DOID:0080240]

|

|

|

|-

| X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques

| class of disease

| Olmsted syndrome
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112012 DOID:0112012]

|

|

|

|-

| X-linked nephrolithiasis type I

| class of disease

| renal tubular transport disease
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111798 DOID:0111798]

|

|

|

|-

| X-linked recessive hypoparathyroidism

| class of disease

| hypoparathyroidism, familial isolated
hypoparathyroidism
X-linked disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111388 DOID:0111388]

|

|

|

|-

| X-linked retinitis pigmentosa and sinorespiratory infections

| class of disease

| syndrome
X-linked disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112124 DOID:0112124]

|

|

|

|-

| X-linked severe congenital neutropenia

| class of disease

| X-linked recessive disease
severe congenital neutropenia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112128 DOID:0112128]

|

|

|

|-

| X-linked sideroblastic anemia

| class of disease

| Hereditary sideroblastic anemia
X-linked recessive disease
sideroblastic anaemia P

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060063 DOID:0060063]

|

|

|

|-

| X-linked spermatogenic failure 1

| class of disease

| Sertoli cell-only syndrome

| Sertoli cell-only syndrome characterized by X-linked inheritance

| [http://www.disease-ontology.org/?id=DOID:0070189 DOID:0070189]

|

|

|

|-

| X-linked spermatogenic failure 2

| class of disease

| azoospermia
X-linked recessive disease

| azoospermia characterized by meiotic arrest of spermatocytes and mixed testicular atrophy that has material basis in X-linked inheritance of mutation in the TEX11 gene on chromosome Xq13

| [http://www.disease-ontology.org/?id=DOID:0070185 DOID:0070185]

|

|

|

|-

| X-linked spinal muscular atrophy 2

| class of disease

| X-linked recessive disease
spinal muscular atrophy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111827 DOID:0111827]

|

|

|

|-

| X-linked spinocerebellar ataxia 1

| class of disease

| X-linked recessive disease
X-linked cerebellar ataxia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111829 DOID:0111829]

|

|

|

|-

| X-linked spinocerebellar ataxia 2

| class of disease

| X-linked cerebellar ataxia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111830 DOID:0111830]

|

|

|

|-

| X-linked spinocerebellar ataxia 3

| class of disease

| X-linked cerebellar ataxia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111831 DOID:0111831]

|

|

|

|-

| X-linked spinocerebellar ataxia 5

| class of disease

| X-linked cerebellar ataxia
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111833 DOID:0111833]

|

|

|

|-

| XX male syndrome

| class of disease
syndrome
anatomical abnormality

| disorder of sex development
X chromosome number anomaly with male phenotype
gonadal dysgenesis
disease

| rare congenital condition where an individual with a female genotype has phenotypically male characteristics that can vary between cases

| [http://www.disease-ontology.org/?id=DOID:0111760 DOID:0111760]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.875.253.064.124 C12.050.351.875.253.064.124]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.706.316.064.124 C12.200.706.316.064.124]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.800.316.064.124 C12.800.316.064.124]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.316.064.124 C16.131.939.316.064.124]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.119.064.124 C19.391.119.064.124]

|

|

|-

| Y-linked deafness

| class of disease

| nonsyndromic deafness
Y-linked disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111757 DOID:0111757]

|

|

|

|-

| Y-linked deafness 2

| class of disease

| Y-linked deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111758 DOID:0111758]

|

|

|

|-

| Y-linked disease

| class of disease

| monogenic disease
Y linkage

| monogenic disease that has material basis in muations on the Y chromosome

| [http://www.disease-ontology.org/?id=DOID:0050738 DOID:0050738]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.338 C16.320.338]

|

|

|-

| Y-linked spermatogenic failure 1

| class of disease

| Sertoli cell-only syndrome
Y-linked disease

| Sertoli cell-only syndrome that has material basis in deletions in the Yq11 chromosomal region

| [http://www.disease-ontology.org/?id=DOID:0070186 DOID:0070186]

|

|

|

|-

| Y-linked spermatogenic failure 2

| class of disease

| male infertility
Y-linked disease
spermatogenic failure

| A male infertility characterized by nonobstroctive azoospermia or oligozoospermia that has material basis in interstitial deletions on the Yq11.221 chromosomal region.

| [http://www.disease-ontology.org/?id=DOID:0070187 DOID:0070187]

|

|

|

|-

| Zenker's paralysis

| class of disease

| peripheral neuropathy
common peroneal nerve lesion

| medical condition

| [http://www.disease-ontology.org/?id=DOID:6925 DOID:6925]

|

|

|

|-

| Zollinger–Ellison syndrome

| class of disease

| syndrome
disease

| disease of the digestive tract in which tumors lead to excess acid and peptic ulcers

| [http://www.disease-ontology.org/?id=DOID:0050782 DOID:0050782]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.730.713.988 C04.730.713.988]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.371.883 C06.301.371.883]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.249.883 C06.405.249.883]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.275.800.924 C06.405.469.275.800.924]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.965 C06.405.469.965]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.586.924 C06.405.748.586.924]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.947 C06.405.748.947]

| Zollinger–Ellison syndrome

| File:ZES endo.jpg

|-

| abacavir allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger abacavir

| [http://www.disease-ontology.org/?id=DOID:0040007 DOID:0040007]

|

|

|

|-

| abdominal aortic aneurysm

| class of disease

| aortic aneurysm
disease

| aortic aneurysm that is located in the abdominal aorta

| [http://www.disease-ontology.org/?id=DOID:7693 DOID:7693]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.055.239.075 C14.907.055.239.075]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.109.139.075 C14.907.109.139.075]

| Abdominal aortic aneurysm

| File:AneurysmAortaWithArrows.jpg

|-

| abdominal obesity-metabolic syndrome

| class of disease

| autosomal dominant disease
syndrome

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060611 DOID:0060611]

|

|

|

|-

| abdominal obesity-metabolic syndrome 3

| class of disease

| abdominal obesity-metabolic syndrome

| abdominal obesity-metabolic syndrome that has material basis in heterozygous mutation in the DYRK1B gene on chromosome 19q13

| [http://www.disease-ontology.org/?id=DOID:0060612 DOID:0060612]

|

|

|

|-

| abdominal tuberculosis

| class of disease

| extrapulmonary tuberculosis

| extrapulmonary tuberculosis that is located in gastrointestinal tract, located in peritoneum, located in omentum, located in mesentery, located in liver, located in spleen or located in pancreas

| [http://www.disease-ontology.org/?id=DOID:0050599 DOID:0050599]

|

| Abdominal tuberculosis

|

|-

| abducens nerve neoplasm

| class of disease

| cranial nerve neoplasm
abducens nerve palsy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14125 DOID:14125]

|

|

|

|-

| abducens nerve palsy

| class of disease

| cranial nerve palsy
paralytic squint

| non-neoplastic or neoplastic disorder affecting the abducens nerve (sixth cranial nerve)

| [http://www.disease-ontology.org/?id=DOID:10865 DOID:10865]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.150 C10.292.150]

| Sixth nerve palsy

|

|-

| abnormal pupillary function

| class of disease

| pupil disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11518 DOID:11518]

|

|

|

|-

| abnormal retinal correspondence

| class of disease

| binocular vision disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12668 DOID:12668]

|

|

|

|-

| abnormal threshold of rods

| class of disease

| night blindness

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11874 DOID:11874]

|

|

|

|-

| abnormality of glucagon secretion

| class of disease

| endocrine pancreas disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14427 DOID:14427]

|

|

|

|-

| acalculous cholecystitis

| class of disease

| cholecystitis
cystitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2828 DOID:2828]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.564.263.249 C06.130.564.263.249]

|

|

|-

| acanthocephaliasis

| class of disease

| parasitic helminthiasis infectious disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050254 DOID:0050254]

|

|

|

|-

| acantholytic acanthoma

| class of disease

| acanthoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4324 DOID:4324]

|

|

|

|-

| acantholytic squamous cell skin carcinoma

| class of disease

| cutaneous squamous-cell carcinoma
keratinizing squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7643 DOID:7643]

|

|

|

|-

| acantholytic variant squamous cell breast carcinoma

| class of disease

| breast squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7459 DOID:7459]

|

|

|

|-

| acanthoma

| class of disease

| squamous cell neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:174 DOID:174]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.700.040 C04.557.470.700.040]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.805.040 C04.588.805.040]

|

|

|-

| acanthosis nigricans

| class of disease

| pigmentation disorder
disease

| A skin condition characterised by dark, velvety patches in body folds and creases.

| [http://www.disease-ontology.org/?id=DOID:3138 DOID:3138]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.621.430.530.100 C17.800.621.430.530.100]

| Acanthosis nigricans

| File:Acanthosis-nigricans4.jpg

|-

| accessory nerve disease

| class of disease

| glossopharyngeal nerve disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:339 DOID:339]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.175 C10.292.175]

| Nervus accessorius

|

|-

| accommodative esotropia

| class of disease

| esotropia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9839 DOID:9839]

|

|

|

|-

| accommodative spasm

| class of disease

| eye accommodation disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11637 DOID:11637]

|

|

|

|-

| achalasia

| class of disease

| esophageal disease
disease

| esophageal disease characterized by an inability of the esophagus to move food toward the stomach resulting from the lower esophogeal sphincter not fully relaxing during swallowing

| [http://www.disease-ontology.org/?id=DOID:9164 DOID:9164]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.117.119.500.432 C06.405.117.119.500.432]

| Achalasia

|

|-

| achilles bursitis

| class of disease

| bursitis
foot diseases
Achilles tendinitis

| bursitis (inflammation of synovial sac) of bursa situated above the insertion of tendon to calcaneus

| [http://www.disease-ontology.org/?id=DOID:12857 DOID:12857]

|

|

|

|-

| achondrogenesis type IA

| class of disease

| achondrogenesis

| achondrogenesis that results in abnormal ossification of the located in vertebral column or located in spine

| [http://www.disease-ontology.org/?id=DOID:0080054 DOID:0080054]

|

|

|

|-

| achondrogenesis type IB

| class of disease

| achondrogenesis
autosomal recessive disease

| achondrogenesis that has material basis in mutation in the SLC26A2 gene which results in umbilical or inguinal hernia and a prominent rounded abdomen

| [http://www.disease-ontology.org/?id=DOID:0080055 DOID:0080055]

|

|

|

|-

| achondrogenesis type II

| class of disease

| achondrogenesis
autosomal dominant disease
spinal disease

| achondrogenesis that has material basis in mutations in the COL2A1 gene which results in underdeveloped lungs, hydrops fetalis, a prominent forehead and abnormal ossification of the located in vertebral column or located in pelvis

| [http://www.disease-ontology.org/?id=DOID:0080056 DOID:0080056]

|

|

|

|-

| achromatopsia 2

| class of disease

| achromatopsia
autosomal recessive disease

| An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11.

| [http://www.disease-ontology.org/?id=DOID:0110007 DOID:0110007]

|

|

|

|-

| achromatopsia 3

| class of disease

| achromatopsia
autosomal recessive disease

| An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the CNGB3 gene on chromosome 8q2.

| [http://www.disease-ontology.org/?id=DOID:0110008 DOID:0110008]

|

|

|

|-

| achromatopsia 4

| class of disease

| achromatopsia

| achromatopsia that has material basis in homozygous or compound heterozygous mutation in the GNAT2 gene (139340) on chromosome 1p13

| [http://www.disease-ontology.org/?id=DOID:0110010 DOID:0110010]

|

|

|

|-

| achromatopsia 7

| class of disease

| achromatopsia
autosomal recessive disease

| An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the ATF6 gene on chromosome 1q23.

| [http://www.disease-ontology.org/?id=DOID:0110009 DOID:0110009]

|

|

|

|-

| acid anhydride respiratory allergy

| class of disease

| respiratory allergy

| respiratory allergy that has allergic trigger acid anhydride

| [http://www.disease-ontology.org/?id=DOID:0040081 DOID:0040081]

|

|

|

|-

| acinar cell carcinoma

| class of disease

| carcinoma

| carcinoma that has material basis in abnormally proliferating cells, derives from spindle cells and/or derives from giant cells

| [http://www.disease-ontology.org/?id=DOID:3025 DOID:3025]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.215 C04.557.470.200.025.215]

|

|

|-

| acinar cell cystadenocarcinoma

| class of disease

| pancreatic cystadenocarcinoma
cystadenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7729 DOID:7729]

|

|

|

|-

| acinic cell breast carcinoma

| class of disease

| breast adenocarcinoma
invasive ductal carcinoma
acinar cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5743 DOID:5743]

|

|

|

|-

| acquired angioedema

| class of disease

| angioedema

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080941 DOID:0080941]

|

|

|

|-

| acquired color blindness

| class of disease

| color blindness

| human disease

| [http://www.disease-ontology.org/?id=DOID:13912 DOID:13912]

|

|

|

|-

| acquired gastric outlet stenosis

| class of disease

| pyloric stenosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14099 DOID:14099]

|

|

|

|-

| acquired generalized lipodystrophy

| class of disease

| lipodystrophy
complete generalized lipodystrophy
rare skin disease
insulin resistance
acquired lipodystrophy

| complete generalized lipodystrophy that is charcterized by generalized disappearance of fat occurring during childhood and adolescence where normal body fat is present at birth

| [http://www.disease-ontology.org/?id=DOID:0080300 DOID:0080300]

|

|

|

|-

| acquired hemangioma

| class of disease

| hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:492 DOID:492]

|

|

|

|-

| acquired hyperkeratosis

| class of disease

| keratosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13072 DOID:13072]

|

|

|

|-

| acquired metabolic disease

| class of disease

| metabolic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060158 DOID:0060158]

|

|

|

|-

| acquired night blindness

| class of disease

| nutritional deficiency disease
night blindness

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11491 DOID:11491]

|

|

|

|-

| acquired polycythemia

| class of disease

| polycythemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2834 DOID:2834]

|

|

|

|-

| acquired tear duct stenosis

| class of disease

| lacrimal apparatus disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13655 DOID:13655]

|

|

|

|-

| acquired thrombocytopenia

| class of disease

| thrombocytopenia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11126 DOID:11126]

|

|

|

|-

| acquired von Willebrand syndrome

| class of disease

| blood coagulation disease
von Willebrand's disease
rare hemorrhagic disorder due to an acquired coagulation factor defect

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111146 DOID:0111146]

|

|

|

|-

| acral lentiginous melanoma

| class of disease

| skin melanoma
disease

| kind of lentiginous skin melanoma

| [http://www.disease-ontology.org/?id=DOID:6367 DOID:6367]

|

|

| File:Skin Tumors-010.jpg

|-

| acrocephalosyndactylia

| class of disease

| synostosis
craniosynostosis
syndactyly
disease

| group of diseases

| [http://www.disease-ontology.org/?id=DOID:12960 DOID:12960]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.099.370.894.232.015 C05.116.099.370.894.232.015]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.099.370.894.819.100 C05.116.099.370.894.819.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.660.207.240.100 C05.660.207.240.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.660.585.800.100 C05.660.585.800.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.660.906.364.100 C05.660.906.364.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.660.906.819.100 C05.660.906.819.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.621.207.240.100 C16.131.621.207.240.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.621.585.800.100 C16.131.621.585.800.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.621.906.364.100 C16.131.621.906.364.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.621.906.819.100 C16.131.621.906.819.100]

| Acrocephalosyndactyly

|

|-

| acrodermatitis

| class of disease

| dermatitis
Foot Dermatoses

| dermatitis that selectively affects the hands and feet

| [http://www.disease-ontology.org/?id=DOID:2722 DOID:2722]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.831.066 C16.131.831.066]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.174.100 C17.800.174.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.804.066 C17.800.804.066]

| Acrodermatitis

|

|-

| acrodermatitis chronica atrophicans

| class of disease

| acrodermatitis
Lyme disease

| An acrodermatitis characterized by a chronically progressive course, leading to widespread atrophy of the skin. It is a clinical manifestation of Lyme borreliosis.

| [http://www.disease-ontology.org/?id=DOID:0060344 DOID:0060344]

|

|

|

|-

| acrofacial dysostosis

| class of disease

| dysostosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060379 DOID:0060379]

|

|

|

|-

| acropustulosis

| class of disease

| dermatitis
acrodermatitis
pustulosis
genodermatosis
other epidermal disorder
genetic epidermal disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4398 DOID:4398]

|

| Acropustulosis

|

|-

| acrorenal syndrome

| class of disease

| syndrome
autosomal recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060347 DOID:0060347]

|

|

|

|-

| actinic keratosis

| class of disease

| pre-malignant neoplasm
dermatoheliosis
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:8866 DOID:8866]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.834.450 C04.834.450]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.428.570 C17.800.428.570]

| Actinic keratosis

| File:Actinic keratosis on the lip.JPEG

|-

| activated PI3K delta syndrome

| class of disease

| agammaglobulinemia
combined immunodeficiency
autosomal dominant disease

| medical condition

| [http://www.disease-ontology.org/?id=DOID:0111936 DOID:0111936]

|

|

| File:Autosomal dominant - en.svg

|-

| active cochlear Meniere's disease

| class of disease

| Meniere's disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13492 DOID:13492]

|

|

|

|-

| active cochleovestibular Meniere's disease

| class of disease

| Meniere's disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13490 DOID:13490]

|

|

|

|-

| active peptic ulcer disease

| class of disease

| peptic ulcer disease
stomach bleeding

| Human disease

| [http://www.disease-ontology.org/?id=DOID:749 DOID:749]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.227.700 C06.405.227.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.414.788.700 C23.550.414.788.700]

|

|

|-

| active vestibular Meniere's disease

| class of disease

| Meniere's disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13491 DOID:13491]

|

|

|

|-

| acute T cell leukemia

| class of disease

| T-cell leukemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5603 DOID:5603]

|

|

|

|-

| acute allergic serous otitis media

| class of disease

| acute serous otitis media
allergy

| acute serous otitis media caused by an allergen

| [http://www.disease-ontology.org/?id=DOID:11558 DOID:11558]

|

|

|

|-

| acute apical periodontitis

| class of disease

| periapical periodontitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11693 DOID:11693]

|

|

|

|-

| acute asthma

| class of disease

| asthma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080810 DOID:0080810]

|

|

|

|-

| acute basophilic leukemia

| class of disease

| acute myeloid leukemia
bilineal acute myeloid leukemia

| rare acute myeloid leukemia in which the immature cells differentiate towards basophils

| [http://www.disease-ontology.org/?id=DOID:0080795 DOID:0080795]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.539.275.125 C04.557.337.539.275.125]

|

|

|-

| acute biphenotypic leukaemia

| class of disease

| mixed phenotype acute leukemia
acute lymphocytic leukemia
acute leukemia
lymphoma
disease

| uncommon type of leukemia which arises in multipotent progenitor cells which have the ability differentiating into both myeloid and lymphoid lineages

| [http://www.disease-ontology.org/?id=DOID:9953 DOID:9953]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.428.100 C04.557.337.428.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.560.100 C15.604.515.560.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.528.100 C20.683.515.528.100]

|

|

|-

| acute canaliculitis

| class of disease

| acute inflammation of lacrimal passage
canaliculitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6969 DOID:6969]

|

|

|

|-

| acute cervicitis

| class of disease

| cervicitis
acute disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:10616 DOID:10616]

|

|

|

|-

| acute chest syndrome

| class of disease

| lung disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1584 DOID:1584]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.074 C08.381.074]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.618.009 C08.618.009]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.141.150.150.219 C15.378.071.141.150.150.219]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.420.155.219 C15.378.420.155.219]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.070.150.219 C16.320.070.150.219]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.365.155.219 C16.320.365.155.219]

|

|

|-

| acute cholangitis

| class of disease

| ascending cholangitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14271 DOID:14271]

|

|

|

|-

| acute closed-angle glaucoma

| class of disease

| primary angle-closure glaucoma

| glaucoma

| [http://www.disease-ontology.org/?id=DOID:13862 DOID:13862]

|

|

| File:Acute Angle Closure-glaucoma.jpg

|-

| acute conjunctivitis

| class of disease

| conjunctivitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11184 DOID:11184]

|

|

|

|-

| acute contagious conjunctivitis

| class of disease

| acute conjunctivitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11213 DOID:11213]

|

|

|

|-

| acute cor pulmonale

| class of disease

| acute pulmonary heart disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8517 DOID:8517]

|

|

|

|-

| acute dacryoadenitis

| class of disease

| dacryoadenitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:952 DOID:952]

|

|

|

|-

| acute dacryocystitis

| class of disease

| dacryocystitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12996 DOID:12996]

|

|

|

|-

| acute diarrhea

| class of disease
symptom or sign

| diarrhea

| diarrhea that is of rapid onset and course characterized by frequent loose or liquid bowel movements. Acute diarrhea is a common cause of death in developing countries and the second most common cause of infant deaths worldwide

| [http://www.disease-ontology.org/?id=DOID:0050140 DOID:0050140]

|

|

|

|-

| acute diffuse nephritis

| class of disease

| diffuse glomerulonephritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14066 DOID:14066]

|

|

|

|-

| acute disseminated encephalomyelitis

| class of disease

| encephalomyelitis

| encephalomyelitis characterized by inflammation located in brain and located in spinal cord that damages myelin

| [http://www.disease-ontology.org/?id=DOID:639 DOID:639]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.114.375.225 C10.114.375.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.695.562.225 C10.228.140.695.562.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.314.350.225 C10.314.350.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.258.250.350 C20.111.258.250.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.291.500.829.188 C23.550.291.500.829.188]

|

|

|-

| acute endometritis

| class of disease

| endometritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7528 DOID:7528]

|

|

|

|-

| acute erythroid leukemia

| class of disease

| acute myeloid leukemia

| rare form of acute myeloid leukemia (less than 5% of AML cases) where the myeloproliferation is of erythroblastic precursors.

| [http://www.disease-ontology.org/?id=DOID:0080780 DOID:0080780]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.539.275.325 C04.557.337.539.275.325]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.190.636.276 C15.378.190.636.276]

| Acute erythroid leukemia

|

|-

| acute ethmoiditis

| class of disease

| ethmoid sinusitis
acute disease

| ethmoid sinusitis which lasts for less than 4 weeks

| [http://www.disease-ontology.org/?id=DOID:9506 DOID:9506]

|

|

|

|-

| acute eustachian salpingitis

| class of disease

| otosalpingitis

| otosalpingitis with a sudden onset and a short course

| [http://www.disease-ontology.org/?id=DOID:10550 DOID:10550]

|

|

|

|-

| acute female pelvic peritonitis

| class of disease

| peritonitis
pelvic inflammatory diseases

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9978 DOID:9978]

|

|

|

|-

| acute frontal sinusitis

| class of disease

| frontal sinusitis
acute disease

| frontal sinusitis which lasts for less than 4 weeks

| [http://www.disease-ontology.org/?id=DOID:14225 DOID:14225]

|

|

|

|-

| acute gonococcal cervicitis

| class of disease

| acute cervicitis
gonococcal infectious diseases

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10615 DOID:10615]

|

|

|

|-

| acute gonococcal cystitis

| class of disease

| urinary tract infection
gonococcal infectious diseases

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13690 DOID:13690]

|

|

|

|-

| acute gonococcal endometritis

| class of disease

| acute endometritis
gonococcal infectious diseases

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7527 DOID:7527]

|

|

|

|-

| acute gonococcal epididymo-orchitis

| class of disease

| epididymo-orchitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10802 DOID:10802]

|

|

|

|-

| acute gonococcal prostatitis

| class of disease

| prostatitis
gonococcal infectious diseases

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13943 DOID:13943]

|

|

|

|-

| acute gonococcal salpingitis

| class of disease

| acute salpingitis
gonococcal infectious diseases

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13942 DOID:13942]

|

|

|

|-

| acute hemorrhagic leukoencephalitis

| class of disease

| acute disseminated encephalomyelitis
acute hemorrhagic encephalitis
acute necrotizing encephalitis

| very rare form of acute disseminated encephalomyelitis, characterized by a brief but intense attack of inflammation and necrotizing vasculitis of venules and hemorrhage, and edema

| [http://www.disease-ontology.org/?id=DOID:10992 DOID:10992]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.114.375.225.500 C10.114.375.225.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.114.375.362 C10.114.375.362]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.695.562.225.500 C10.228.140.695.562.225.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.695.562.375 C10.228.140.695.562.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.314.350.225.500 C10.314.350.225.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.314.350.375 C10.314.350.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.258.250.350.500 C20.111.258.250.350.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.258.250.425 C20.111.258.250.425]

|

|

|-

| acute hemorrhagic pancreatitis

| class of disease

| acute pancreatitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080999 DOID:0080999]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.689.750.325 C06.689.750.325]

|

|

|-

| acute hydrops keratoconus

| class of disease

| keratoconus
eye disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10125 DOID:10125]

|

| Corneal hydrops

|

|-

| acute infantile liver failure-multisystemic involvement syndrome

| class of disease

| liver failure, infantile
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080717 DOID:0080717]

|

|

|

|-

| acute infection of pinna

| class of disease

| otitis externa

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10520 DOID:10520]

|

|

|

|-

| acute inflammation of lacrimal passage

| class of disease

| lacrimal apparatus disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6970 DOID:6970]

|

|

|

|-

| acute kidney tubular necrosis

| class of disease

| acute kidney injury
disease

| medical condition involving the death of tubular epithelial cells that form the renal tubules of the kidneys

| [http://www.disease-ontology.org/?id=DOID:12556 DOID:12556]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.968.419.780.050.500 C12.050.351.968.419.780.050.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.777.419.780.050.500 C12.200.777.419.780.050.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.950.419.780.050.500 C12.950.419.780.050.500]

|

|

|-

| acute laryngitis

| class of disease

| laryngitis

| respiratory disease

| [http://www.disease-ontology.org/?id=DOID:9396 DOID:9396]

|

|

|

|-

| acute laryngopharyngitis

| class of disease

| upper respiratory tract disease
laryngopharyngitis

| respiratory disease

| [http://www.disease-ontology.org/?id=DOID:11195 DOID:11195]

|

|

|

|-

| acute leukemia

| class of disease

| leukemia
lymphoblastic leukemia
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:12603 DOID:12603]

|

| Acute leukemias

|

|-

| acute lymphocytic leukemia

| class of disease

| acute leukemia
lymphoblastic leukemia
disease

| leukemia that is characterized by over production of lymphoblasts.

| [http://www.disease-ontology.org/?id=DOID:9952 DOID:9952]

|

| Acute lymphoblastic leukemia

| File:Acute leukemia-ALL.jpg

|-

| acute maxillary sinusitis

| class of disease

| maxillary sinusitis
acute disease

| maxillary sinusitis which lasts for less than 4 weeks

| [http://www.disease-ontology.org/?id=DOID:2050 DOID:2050]

|

|

|

|-

| acute megakaryoblastic leukemia

| class of disease

| acute myeloid leukemia
leukemia
bilineal acute myeloid leukemia

| leukemia that derives from blood-forming tissue in which megakaryocytes proliferate in the bone marrow and circulate in the blood in large numbers

| [http://www.disease-ontology.org/?id=DOID:8761 DOID:8761]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.539.275.450 C04.557.337.539.275.450]

|

|

|-

| acute monocytic leukemia

| class of disease

| monocytic leukemia
acute myeloid leukemia
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8864 DOID:8864]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.539.275.484 C04.557.337.539.275.484]

| Acute monocytic leukemia

|

|-

| acute myeloid leukemia

| class of disease

| acute leukemia
myeloid leukemia
disease

| myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells

| [http://www.disease-ontology.org/?id=DOID:9119 DOID:9119]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.539.275 C04.557.337.539.275]

| Acute myeloid leukemia

| File:Auer rods.PNG

|-

| acute myeloid leukemia with BCR-ABL1

| class of disease

| acute myeloid leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080976 DOID:0080976]

|

|

|

|-

| acute myocardial infarction

| class of disease

| myocardial infarction
acute coronary syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:9408 DOID:9408]

|

|

|

|-

| acute myocarditis

| class of disease

| myocarditis

| human disease

| [http://www.disease-ontology.org/?id=DOID:3951 DOID:3951]

|

|

|

|-

| acute necrotizing encephalitis

| class of disease

| encephalitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5222 DOID:5222]

|

|

|

|-

| acute orbital inflammation

| class of disease

| orbital disease
inflammation

| human disease

| [http://www.disease-ontology.org/?id=DOID:11230 DOID:11230]

|

|

|

|-

| acute pancreatitis

| class of disease

| pancreatitis
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2913 DOID:2913]

|

| Acute pancreatitis

| File:3D Medical Animation Acute Pancreatitis.jpg

|-

| acute pericementitis

| class of disease

| periodontitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10423 DOID:10423]

|

|

|

|-

| acute perichondritis of pinna

| class of disease

| perichondritis of auricle

| human disease

| [http://www.disease-ontology.org/?id=DOID:221 DOID:221]

|

|

|

|-

| acute poststreptococcal glomerulonephritis

| class of disease

| glomerulonephritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14064 DOID:14064]

|

|

|

|-

| acute proliferative glomerulonephritis

| class of disease

| glomerulonephritis
proliferative glomerulonephritis
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13138 DOID:13138]

|

| Acute proliferative glomerulonephritis

|

|-

| acute promyelocytic leukemia

| class of disease
symptom or sign

| acute myeloid leukemia
bilineal acute myeloid leukemia
disease

| acute myeloid leukemia characterized by accumulation of promyelocytes in the bone marrow and by a translocation between chromosomes 15 and 17

| [http://www.disease-ontology.org/?id=DOID:0060318 DOID:0060318]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.539.275.700 C04.557.337.539.275.700]

| Acute promyelocytic leukemia

| File:Жедел промиелоцитарлы лейкоз (миелограмма).jpg

|-

| acute pulmonary heart disease

| class of disease

| cor pulmonale

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8514 DOID:8514]

|

|

|

|-

| acute retinal necrosis syndrome

| class of disease

| retinitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3611 DOID:3611]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.768.773.674 C11.768.773.674]

|

|

|-

| acute retrobulbar neuritis

| class of disease

| optic neuritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14155 DOID:14155]

|

|

|

|-

| acute salpingitis

| class of disease

| salpingitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10973 DOID:10973]

|

|

|

|-

| acute salpingo-oophoritis

| class of disease

| salpingo-oophoritis
acute salpingitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10971 DOID:10971]

|

|

|

|-

| acute serous otitis media

| class of disease

| acute transudative otitis media
serous glue ear

| acute transudative otitis media with thin, watery and sterile effusion

| [http://www.disease-ontology.org/?id=DOID:11557 DOID:11557]

|

|

|

|-

| acute sphenoidal sinusitis

| class of disease

| sphenoid sinusitis
acute disease

| sphenoid sinusitis which lasts for less than 4 weeks

| [http://www.disease-ontology.org/?id=DOID:13046 DOID:13046]

|

|

|

|-

| acute stress disorder

| class of disease

| anxiety disorder
stress-related disorders
disease

| psychological response to a terrifying, traumatic, or surprising experience

| [http://www.disease-ontology.org/?id=DOID:6088 DOID:6088]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.950.750.550 F03.950.750.550]

|

|

|-

| acute thyroiditis

| class of disease

| thyroiditis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14353 DOID:14353]

|

|

|

|-

| acute tympanitis

| class of disease

| tympanic membrane disease
myringitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13790 DOID:13790]

|

|

|

|-

| acute vascular insufficiency of intestine

| class of disease

| intestinal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8590 DOID:8590]

|

|

|

|-

| adamantinoid basal cell epithelioma

| class of disease

| basal-cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4290 DOID:4290]

|

|

|

|-

| adamantinoma

| class of disease

| bone cancer
disease

| bone cancer that is located in almost exclusively in the long bones

| [http://www.disease-ontology.org/?id=DOID:2776 DOID:2776]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.149.030 C04.588.149.030]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.231.030 C05.116.231.030]

| Adamantinoma

|

|-

| adamantinous craniopharyngioma

| class of disease

| craniopharyngioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3846 DOID:3846]

|

|

|

|-

| adenocarcinoma

| class of disease

| carcinoma
disease

| carcinoma that has material basis in abnormally proliferating cells, derives from epithelial cells, which originate in glandular tissue

| [http://www.disease-ontology.org/?id=DOID:299 DOID:299]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025 C04.557.470.200.025]

| Adenocarcinomas

| File:Adenocarcinoma of the Sigmoid Colon (longitudinal section, closeup).jpg

|-

| adenocarcinoma in situ

| class of disease

| in situ carcinoma
adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4943 DOID:4943]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.014 C04.557.470.200.025.014]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.240.124 C04.557.470.200.240.124]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.149.249 C23.149.249]

|

|

|-

| adenocarcinoma of the lung

| class of disease

| lung cancer
adenocarcinoma

| non-small cell lung carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:3910 DOID:3910]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.022 C04.557.470.200.025.022]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.894.797.520.055 C04.588.894.797.520.055]

|

|

|-

| adenofibroma

| class of disease

| benign neoplasms by histologic type
fibroma

| cell type benign neoplasm that is composed of glandular and fibrous tissues, with a relatively large proportion of glands

| [http://www.disease-ontology.org/?id=DOID:2683 DOID:2683]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.590.595.050 C04.557.450.565.590.595.050]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.625.050 C04.557.470.625.050]

|

|

|-

| adenoid basal cell carcinoma

| class of disease

| basal-cell carcinoma
tonsil cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4294 DOID:4294]

|

|

|

|-

| adenoid cystic carcinoma

| class of disease

| cancer
cylindroma
carcinoma
tonsil cancer

| type of cancer

| [http://www.disease-ontology.org/?id=DOID:0080202 DOID:0080202]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.220 C04.557.470.200.025.220]

| Adenoid cystic carcinoma

| File:Adenoid cystic carcinoma - intermed mag.jpg

|-

| adenoid hypertrophy

| class of disease

| upper respiratory tract disease

| upper respiratory tract disease characterized by the unusual growth of the adenoid tonsil; has symptom snoring, has symptom hyponasality, has symptom otitis media with effusion, has symptom mouth breathing

| [http://www.disease-ontology.org/?id=DOID:0060311 DOID:0060311]

|

| Adenoid hypertrophy

| File:Adenoid hypertrophy.jpg

|-

| adenoiditis

| class of disease

| upper respiratory tract disease
nasopharyngitis

| inflammation of the adenoid tissue

| [http://www.disease-ontology.org/?id=DOID:0050145 DOID:0050145]

|

|

|

|-

| adenoma

| class of disease

| benign neoplasms by histologic type
disease

| cell type benign neoplasm that is composed of epithelial tissue in which tumor cells form glands or glandlike structures

| [http://www.disease-ontology.org/?id=DOID:657 DOID:657]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.035 C04.557.470.035]

| Adenomas

| File:Colon adenoma (1).jpg

|-

| adenomatoid tumor

| class of disease

| benign neoplasm
benign mesothelioma

| type of tumor

| [http://www.disease-ontology.org/?id=DOID:746 DOID:746]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.035.200 C04.557.470.035.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.660.200 C04.557.470.660.200]

| Adenomatoid tumors

|

|-

| adenomyoma

| class of disease

| carcinosarcoma
carcinoma

| carcinosarcoma that has material basis in gland and muscle components

| [http://www.disease-ontology.org/?id=DOID:2609 DOID:2609]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.435.110 C04.557.435.110]

| Adenomyomas

|

|-

| adenomyoma of uterine corpus

| class of disease

| adenomyoma
uterine corpus cancer
carcinosarcoma of the corpus uteri
uterine benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4994 DOID:4994]

|

|

|

|-

| adenomyosis

| class of disease

| endometriosis
uterine disease
disease

| extension of endometrial tissue into the myometrium

| [http://www.disease-ontology.org/?id=DOID:288 DOID:288]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.852.113 C13.351.500.852.113]

| Adenomyosis of the uterus

|

|-

| adenosarcoma

| class of disease

| carcinosarcoma

| carcinosarcoma that derives from simultaneously or consecutively in mesodermal tissue and glandular epithelium

| [http://www.disease-ontology.org/?id=DOID:1974 DOID:1974]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.435.135 C04.557.435.135]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.135 C04.557.450.795.135]

|

|

|-

| adenosquamous bile duct carcinoma

| class of disease

| squamous cell carcinoma
bile duct cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:5624 DOID:5624]

|

|

|

|-

| adenosquamous breast carcinoma

| class of disease

| breast squamous cell carcinoma
adenosquamous carcinoma
breast cancer
squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5623 DOID:5623]

|

|

|

|-

| adenosquamous carcinoma

| class of disease

| squamous cell carcinoma
disease

| squamous cell carcinoma that contains squamous cells and gland-like cells

| [http://www.disease-ontology.org/?id=DOID:4830 DOID:4830]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.435.250 C04.557.435.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.150 C04.557.470.200.150]

| Adenosquamous carcinoma

|

|-

| adenosquamous cell lung carcinoma

| class of disease

| adenosquamous carcinoma
squamous cell carcinoma of the lung
squamous cell carcinoma
lung cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4829 DOID:4829]

|

|

|

|-

| adenosquamous gallbladder carcinoma

| class of disease

| gallbladder squamous cell carcinoma
adenosquamous carcinoma
squamous cell carcinoma
gallbladder cancer
gallbladder carcinoma

| gallbladder carcinoma that derives from squamous cells and gland-like cells

| [http://www.disease-ontology.org/?id=DOID:5627 DOID:5627]

|

|

|

|-

| adenosquamous pancreas carcinoma

| class of disease

| adenosquamous carcinoma
squamous cell carcinoma of pancreas
squamous cell carcinoma
pancreatic cancer

| pancreatic ductal carcinoma that derives from squamous cells and gland-like cells

| [http://www.disease-ontology.org/?id=DOID:5637 DOID:5637]

|

|

|

|-

| adenosquamous prostate carcinoma

| class of disease

| adenosquamous carcinoma
squamous cell carcinoma
prostate cancer

| prostate carcinoma that derives from squamous cells and gland-like cells

| [http://www.disease-ontology.org/?id=DOID:5634 DOID:5634]

|

|

|

|-

| adenoviral keratoconjunctivitis

| class of disease

| viral conjunctivitis
keratoconjunctivitis
adenovirus infection

| common and highly contagious viral infection of the eye

| [http://www.disease-ontology.org/?id=DOID:13014 DOID:13014]

|

| Adenoviral keratoconjunctivitis

|

|-

| adhesions of uterus

| class of disease

| gynatresia
uterine disease
disease

| adhesions or fibrosis of endometrium of uterus

| [http://www.disease-ontology.org/?id=DOID:13812 DOID:13812]

|

| Asherman's syndrome

|

|-

| adhesive otitis media

| class of disease

| ear disease
otitis media
adhesive middle ear disease

| An auditory system disease that is characterized by a thin retracted ear drum becomes sucked into the middle-ear space and stuck (i.e., adherent) to the ossicles and other bones of the middle ear.

| [http://www.disease-ontology.org/?id=DOID:11235 DOID:11235]

|

|

|

|-

| adiposis dolorosa

| class of disease

| lipomatosis
subcutaneous tissue disease

| rare condition characterized by generalized obesity and fatty tumors in the adipose tissue.

| [http://www.disease-ontology.org/?id=DOID:3928 DOID:3928]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.463.249 C17.800.463.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.718.500 C18.452.584.718.500]

| Adiposis dolorosa

| File:Nervous and mental diseases (1919) (14781727145).jpg

|-

| adjustment disorder

| class of disease

| mental disorder
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:507 DOID:507]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.950.500 F03.950.500]

| Adjustment disorder

|

|-

| adolescence-adult electroclinical syndrome

| class of disease

| electroclinical syndrome
absence seizure

| electroclinical syndrome with onset in adolescence and adulthood

| [http://www.disease-ontology.org/?id=DOID:0050705 DOID:0050705]

|

|

|

|-

| adrenal adenoma

| class of disease

| endocrine organ benign neoplasm
adrenal gland disease
benign epithelial neoplasm
benign neoplasm of adrenal gland
adenoma
disease

| endocrine organ benign neoplasm, a benign tumor of the glandular type (adenoma) in the adrenal gland

| [http://www.disease-ontology.org/?id=DOID:656 DOID:656]

|

|

|

|-

| adrenal carcinoma

| class of disease

| adrenal gland cancer
carcinoma

| adrenal cancer that is located in the cortex (steroid hormone-producing tissue) of the adrenal gland and that has material basis in abnormally proliferating cells derives from epithelial cells

| [http://www.disease-ontology.org/?id=DOID:3950 DOID:3950]

|

|

|

|-

| adrenal cortex cancer

| class of disease

| adrenal gland cancer
adrenal cortex neoplasm
adrenal cortex disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:660 DOID:660]

|

| Cancers of adrenal glands

|

|-

| adrenal cortex disease

| class of disease

| adrenal gland disease

| disease involving the adrenal cortex

| [http://www.disease-ontology.org/?id=DOID:3952 DOID:3952]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.053.098 C19.053.098]

|

|

|-

| adrenal cortical adenocarcinoma

| class of disease

| adrenocortical carcinoma
adenocarcinoma

| adrenalcortical carcinoma that originating in the cortex of the adrenal gland and derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:3959 DOID:3959]

|

|

|

|-

| adrenal cortical hypofunction

| class of disease

| adrenal cortex disease
primary adrenal insufficiency

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10493 DOID:10493]

|

|

|

|-

| adrenal gland cancer

| class of disease

| endocrine gland cancer
adrenal gland neoplasm
adrenal gland disease

| endocrine gland cancer located in the adrenal glands which are located above the kidneys

| [http://www.disease-ontology.org/?id=DOID:3953 DOID:3953]

|

|

|

|-

| adrenal gland disease

| class of disease

| endocrine system disease

| endocrine disease

| [http://www.disease-ontology.org/?id=DOID:9553 DOID:9553]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.053 C19.053]

| Diseases and disorders of adrenal glands/hormones

|

|-

| adrenal gland ganglioneuroblastoma

| class of disease

| adrenal gland cancer
adrenal neuroblastoma
peripheral nervous system ganglioneuroblastoma
malignant peripheral nerve neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8140 DOID:8140]

|

|

|

|-

| adrenal gland hyperfunction

| class of disease

| adrenal cortex disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3947 DOID:3947]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.053.800 C19.053.800]

|

|

|-

| adrenal gland pheochromocytoma

| class of disease

| phaeochromocytoma
malignant pheochromocytoma

| adrenal medulla cancer that is characterized by overproduction of adrenaline

| [http://www.disease-ontology.org/?id=DOID:0050892 DOID:0050892]

|

|

|

|-

| adrenal medulla cancer

| class of disease

| adrenal gland cancer
adrenal medulla neoplasm

| adrenal gland cancer that is located in the adrenal medulla

| [http://www.disease-ontology.org/?id=DOID:5719 DOID:5719]

|

|

|

|-

| adrenal medulla carcinoma

| class of disease

| adrenal medulla cancer
carcinoma

| adrenal medulla cancer that has material basis in abnormally proliferating cells derives from epithelial cells

| [http://www.disease-ontology.org/?id=DOID:7379 DOID:7379]

|

|

|

|-

| adrenal neuroblastoma

| class of disease

| adrenal gland cancer
nervous system cancer
adrenal medulla cancer
endocrine gland cancer
neuroblastoma

| adrenal gland cancer that derives from immature neuroblastic cells

| [http://www.disease-ontology.org/?id=DOID:5718 DOID:5718]

|

| Neuroblastoma of the adrenal glands

|

|-

| adrenal rest tumor

| class of disease

| endocrine organ benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1786 DOID:1786]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.035.232 C04.557.470.035.232]

|

|

|-

| adrenocortical adenoma

| class of disease

| adrenal adenoma

| adrenal adenoma that is a benign tumor of the adrenal cortex

| [http://www.disease-ontology.org/?id=DOID:0050891 DOID:0050891]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.078.265.500 C04.588.322.078.265.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.053.098.265.500 C19.053.098.265.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.053.347.500.500 C19.053.347.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.078.265.500 C19.344.078.265.500]

| Adrenocortical adenoma

|

|-

| adult acute lymphocytic leukemia

| class of disease

| acute lymphocytic leukemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5604 DOID:5604]

|

|

|

|-

| adult acute monocytic leukemia

| class of disease

| acute monocytic leukemia

| acute monocytic leukemia occurring in adults

| [http://www.disease-ontology.org/?id=DOID:0080149 DOID:0080149]

|

|

|

|-

| adult astrocytic tumour

| class of disease

| astrocytoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3076 DOID:3076]

|

|

|

|-

| adult botryoid rhabdomyosarcoma

| class of disease

| botryoid embryo rhabdomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6847 DOID:6847]

|

|

|

|-

| adult brain ependymoma

| class of disease

| brain ependymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7750 DOID:7750]

|

|

|

|-

| adult brain stem glioma

| class of disease

| Brainstem glioma
brain stem cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4813 DOID:4813]

|

|

|

|-

| adult brainstem astrocytoma

| class of disease

| adult brain stem glioma
brain stem astrocytic neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5922 DOID:5922]

|

|

|

|-

| adult brainstem gliosarcoma

| class of disease

| adult brain stem glioma

| human disease

| [http://www.disease-ontology.org/?id=DOID:4812 DOID:4812]

|

|

|

|-

| adult brainstem mixed glioma

| class of disease

| adult brain stem glioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5921 DOID:5921]

|

|

|

|-

| adult central nervous system choriocarcinoma

| class of disease

| choriocarcinoma
central nervous system cancer
central nervous system adult germ cell tumor
central nervous system choriocarcinoma
nervous system cancer
central nervous system disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6634 DOID:6634]

|

|

|

|-

| adult central nervous system embryonal carcinoma

| class of disease

| central nervous system adult germ cell tumor
central nervous system embryonal carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7233 DOID:7233]

|

|

|

|-

| adult central nervous system germinoma

| class of disease

| central nervous system germinoma
central nervous system adult germ cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7867 DOID:7867]

|

|

|

|-

| adult central nervous system immature teratoma

| class of disease

| adult central nervous system teratoma
central nervous system immature teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6018 DOID:6018]

|

|

|

|-

| adult central nervous system mature teratoma

| class of disease

| adult central nervous system teratoma
central nervous system mature teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6016 DOID:6016]

|

|

|

|-

| adult central nervous system mixed germ cell tumor

| class of disease

| central nervous system adult germ cell tumor
mixed germ cell tumor of central nervous system

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7945 DOID:7945]

|

|

|

|-

| adult central nervous system primitive neuroectodermal neoplasm

| class of disease

| central nervous system primitive neuroectodermal neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3865 DOID:3865]

|

|

|

|-

| adult central nervous system teratoma

| class of disease

| central nervous system teratoma
central nervous system adult germ cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6015 DOID:6015]

|

|

|

|-

| adult cerebellar neoplasm

| class of disease

| cerebellum cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5056 DOID:5056]

|

|

|

|-

| adult choroid plexus cancer

| class of disease

| choroid plexus neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3542 DOID:3542]

|

|

|

|-

| adult cystic teratoma

| class of disease

| cystic teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7079 DOID:7079]

|

|

|

|-

| adult dermatomyositis

| class of disease

| dermatomyositis

| Dermatomyositis in an adult

| [http://www.disease-ontology.org/?id=DOID:14202 DOID:14202]

|

|

|

|-

| adult endodermal sinus tumor

| class of disease

| endodermal sinus tumor

| endodermal sinus tumor that occurs in adults

| [http://www.disease-ontology.org/?id=DOID:5348 DOID:5348]

|

|

|

|-

| adult ependymoblastoma

| class of disease

| ependymoblastoma
adult central nervous system primitive neuroectodermal neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7631 DOID:7631]

|

|

|

|-

| adult epithelioid sarcoma

| class of disease

| epithelioid sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8282 DOID:8282]

|

|

|

|-

| adult extraosseous chondrosarcoma

| class of disease

| extraosseous chondrosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7902 DOID:7902]

|

|

|

|-

| adult extraosseous osteosarcoma

| class of disease

| bone cancer
extraosseous osteosarcoma
osteosarcoma

| adult sarcoma of soft tissue and extraosseous osteosarcoma that is located in the soft tissues without direct attachment to the skeletal system and results in the production of osteoid, bone, or chondroid material

| [http://www.disease-ontology.org/?id=DOID:7827 DOID:7827]

|

|

|

|-

| adult familial myoclonic epilepsy 1

| class of disease

| benign adult familial myoclonic epilepsy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111690 DOID:0111690]

|

|

|

|-

| adult familial myoclonic epilepsy 3

| class of disease

| benign adult familial myoclonic epilepsy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111695 DOID:0111695]

|

|

|

|-

| adult fibrosarcoma

| class of disease

| fibrosarcoma
conventional fibrosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3516 DOID:3516]

|

|

|

|-

| adult hepatocellular carcinoma

| class of disease

| hepatocellular carcinoma

| hepatocellular carcinoma is characterized by hepatic mass, abdominal pain and, in advanced stages, jaundice, cachexia and liver failure and often develops in the setting of chronic necro-inflammation

| [http://www.disease-ontology.org/?id=DOID:0070328 DOID:0070328]

|

|

|

|-

| adult hypophosphatasia

| class of disease

| hypophosphatasia

| A hypophosphatasia that has material basis in a heterozygous mutation of ALPL on chromosome 1p36.12.

| [http://www.disease-ontology.org/?id=DOID:0110913 DOID:0110913]

|

|

|

|-

| adult infiltrating astrocytic neoplasm

| class of disease

| adult astrocytic tumour

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7656 DOID:7656]

|

|

|

|-

| adult intracranial malignant hemangiopericytoma

| class of disease

| connective tissue neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6333 DOID:6333]

|

|

|

|-

| adult leptomeningeal melanoma

| class of disease

| meningeal melanoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6090 DOID:6090]

|

|

|

|-

| adult liposarcoma

| class of disease

| liposarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5693 DOID:5693]

|

|

|

|-

| adult lymphoma

| class of disease

| lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5825 DOID:5825]

|

|

|

|-

| adult malignant hemangiopericytoma

| class of disease

| hemangiopericytoma
hemangiopericytoma, malignant

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6332 DOID:6332]

|

|

|

|-

| adult malignant mesenchymoma

| class of disease

| malignant mesenchymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5894 DOID:5894]

|

|

|

|-

| adult malignant schwannoma

| class of disease

| malignant peripheral nerve sheath tumor
childhood malignant schwannoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8369 DOID:8369]

|

|

|

|-

| adult medulloblastoma

| class of disease

| medulloblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3864 DOID:3864]

|

|

|

|-

| adult mesenchymal chondrosarcoma

| class of disease

| mesenchymal chondrosarcoma

| adult sarcoma of soft tissue and mesenchymal chondrosarcoma that is located in the cartilage

| [http://www.disease-ontology.org/?id=DOID:4547 DOID:4547]

|

|

|

|-

| adult myxoid chondrosarcoma

| class of disease

| myxoid chondrosarcoma

| adult sarcoma of soft tissue and myxoid chondrosarcoma that is composed of multiple lobules of chondroblast-like cells, arranged in cords and strands, embedded in a myxoid stroma, and separated by fibrous septa

| [http://www.disease-ontology.org/?id=DOID:6495 DOID:6495]

|

|

|

|-

| adult oligodendroglioma

| class of disease

| oligodendroglioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3186 DOID:3186]

|

|

|

|-

| adult papillary meningioma

| class of disease

| rhabdoid meningioma
papillary meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7826 DOID:7826]

|

|

|

|-

| adult pineal parenchymal tumor

| class of disease

| pinealoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5031 DOID:5031]

|

|

|

|-

| adult pineoblastoma

| class of disease

| adult pineal parenchymal tumor
pinealoblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6648 DOID:6648]

|

|

|

|-

| adult pleomorphic rhabdomyosarcoma

| class of disease

| pleomorphic rhabdomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8251 DOID:8251]

|

|

|

|-

| adult spinal cord ependymoma

| class of disease

| spinal cord ependymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7788 DOID:7788]

|

|

|

|-

| adult spinal cord glioblastoma multiforme

| class of disease

| spinal cord glioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7806 DOID:7806]

|

|

|

|-

| adult teratoma

| class of disease

| teratoma
benign teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5565 DOID:5565]

|

|

|

|-

| adult type testicular granulosa cell tumor

| class of disease

| testicular granulosa cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8394 DOID:8394]

|

|

|

|-

| adult vagina botryoid rhabdomyosarcoma

| class of disease

| vagina botryoid rhabdomyosarcoma
adult botryoid rhabdomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6848 DOID:6848]

|

|

|

|-

| adult xanthogranuloma

| class of disease

| non-Langerhans-cell histiocytosis
xanthogranuloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7875 DOID:7875]

|

|

|

|-

| adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

| class of disease

| leukodystrophy
autosomal dominant disease
Leukoencephalopathy with neuroaxonal spheroids

| leukodystrophy that is characterized by progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy and has material basis in heterozygous mutation in the CSF1R gene on chromosome 5q32

| [http://www.disease-ontology.org/?id=DOID:0080523 DOID:0080523]

|

|

|

|-

| adult-onset severe asthma

| class of disease

| chronic asthma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080816 DOID:0080816]

|

|

|

|-

| adult-onset type II citrullinemia

| class of disease

| citrullinemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070342 DOID:0070342]

|

|

|

|-

| advanced sleep phase syndrome 1

| class of disease

| advanced sleep phase syndrome

| advanced sleep phase syndrome that has material basis in heterozygous mutation in the PER2 gene on chromosome 2q37

| [http://www.disease-ontology.org/?id=DOID:0110011 DOID:0110011]

|

|

|

|-

| afferent loop syndrome

| class of disease

| postgastrectomy syndrome

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8438 DOID:8438]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.531.099 C06.405.469.531.099]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.767.050 C23.550.767.050]

|

|

|-

| aflatoxins-related hepatocellular carcinoma

| class of disease

| hepatocellular carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5022 DOID:5022]

|

|

|

|-

| agammaglobulinemia 5

| class of disease

| autosomal dominant disease
agammaglobulinemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080588 DOID:0080588]

|

|

|

|-

| age related macular degeneration 1

| class of disease

| age related macular degeneration

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110014 DOID:0110014]

|

|

|

|-

| age related macular degeneration 10

| class of disease

| age related macular degeneration
hereditary retinal dystrophy

| An age related macular degeneration associated with variation in the genomic region 9:112,100,000-127,500,000 (GRCh38). TLR4 has been put forth as a candidate gene.

| [http://www.disease-ontology.org/?id=DOID:0110022 DOID:0110022]

|

|

|

|-

| age related macular degeneration 13

| class of disease

| age related macular degeneration
hereditary retinal dystrophy

| age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25

| [http://www.disease-ontology.org/?id=DOID:0110025 DOID:0110025]

|

|

|

|-

| age related macular degeneration 14

| class of disease

| age related macular degeneration
hereditary retinal dystrophy

| age related macular degeneration associated with variation at or near the C2 and CFB genes on chromosome 6p21

| [http://www.disease-ontology.org/?id=DOID:0110026 DOID:0110026]

|

|

|

|-

| age related macular degeneration 15

| class of disease

| age related macular degeneration
hereditary retinal dystrophy

| age related macular degeneration conferred by variation in the C9 gene on chromosome 5p13

| [http://www.disease-ontology.org/?id=DOID:0110027 DOID:0110027]

|

|

|

|-

| age related macular degeneration 5

| class of disease

| age related macular degeneration
hereditary retinal dystrophy

| age related macular degeneration onferred by heterozygous mutation in the ERCC6 gene on chromosome 10q11

| [http://www.disease-ontology.org/?id=DOID:0110028 DOID:0110028]

|

|

|

|-

| aggressive digital papillary adenocarcinoma

| class of disease

| papillary adenocarcinoma
skin carcinoma
adenocarcinoma
sweat gland carcinoma

| medical condition

| [http://www.disease-ontology.org/?id=DOID:5590 DOID:5590]

|

|

|

|-

| aggressive periodontitis

| class of disease

| periodontitis

| periodontitis characterized by rapid attachment loss and bone destruction

| [http://www.disease-ontology.org/?id=DOID:1474 DOID:1474]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.533.161 C07.465.714.533.161]

|

|

|-

| aggressive systemic mastocytosis

| class of disease

| systemic mastocytosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4798 DOID:4798]

|

|

|

|-

| agoraphobia

| class of disease

| phobia
disease

| phobic disorder involving the specific anxiety about being in a place or situation where escape is difficult or embarrassing or where help may be unavailable

| [http://www.disease-ontology.org/?id=DOID:593 DOID:593]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.080.100 F03.080.100]

|

|

|-

| agraphia

| class of disease
symptom or sign

| writing disorder
aphasia
disease

| disease that results in the loss of the ability to write

| [http://www.disease-ontology.org/?id=DOID:0060223 DOID:0060223]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.606.150.500.050 C10.597.606.150.500.050]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.604.150.500.050 C23.888.592.604.150.500.050]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.606.150.550.700.125 C10.597.606.150.550.700.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.604.150.550.700.125 C23.888.592.604.150.550.700.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.625.374.188.700.125 F03.625.374.188.700.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.625.562.700.125 F03.625.562.700.125]

|

|

|-

| ainhum

| class of disease

| connective tissue disease
foot diseases
genetic disease
autoamputation
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11329 DOID:11329]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.264.143 C05.116.264.143]

| Ainhum

| File:Ainhum.jpg

|-

| akinetic mutism

| class of disease

| encephalopathy

| brain disease characterized by marked reduction of nearly all motor functions including facial expressions, gestures and speech output, but with some degree of alertness

| [http://www.disease-ontology.org/?id=DOID:4267 DOID:4267]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.042 C10.228.140.042]

|

|

|-

| akinetopsia

| class of disease

| agnosia
visual perception
motion perception

| agnosia that is a loss of motion perception

| [http://www.disease-ontology.org/?id=DOID:0060130 DOID:0060130]

|

|

|

|-

| alastrim

| class of disease

| smallpox

| milder form of smallpox

| [http://www.disease-ontology.org/?id=DOID:9153 DOID:9153]

|

|

|

|-

| alcohol abuse

| class of disease

| substance abuse
alcohol consumption
alcohol-related disorders

| substance abuse that involves the recurring use of alcoholic beverages despite negative consequences

| [http://www.disease-ontology.org/?id=DOID:1574 DOID:1574]

|

| Alcohol abuse

| File:The Drunkard's Progress 1846.jpg

|-

| alcohol dependence

| class of disease

| non-controlled substance abuse
alcoholism
alcohol abuse

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050741 DOID:0050741]

|

|

|

|-

| alcohol-induced mental disorder

| class of disease

| long-term effects of alcohol consumption
non-controlled substance abuse
substance-induced psychosis

| nental and behavioural disorders due to use of alcohol

| [http://www.disease-ontology.org/?id=DOID:251 DOID:251]

|

|

|

|-

| alcohol-induced psychotic disorder

| class of disease

| alcohol-induced mental disorder
substance-induced psychosis

| organic psychotic states due mainly to excessive consumption of alcoholic beverages

| [http://www.disease-ontology.org/?id=DOID:252 DOID:252]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.723.809.750 C25.723.809.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.775.100.087.750 C25.775.100.087.750]

|

|

|-

| alcohol-related birth defect

| class of disease

| fetal alcohol spectrum disorders

| fetal alcohol spectrum disorder that results in damage to organs, bones, or muscles due to prenatal alcohol exposure

| [http://www.disease-ontology.org/?id=DOID:0050668 DOID:0050668]

|

|

|

|-

| alcohol-related neurodevelopmental disorder

| class of disease

| fetal alcohol spectrum disorders

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050667 DOID:0050667]

|

|

|

|-

| alcoholic cardiomyopathy

| class of disease

| extrinsic cardiomyopathy
long-term effects of alcohol consumption
alcohol and health

| disease in which the chronic long-term abuse of alcohol (i.e., ethanol) leads to heart failure

| [http://www.disease-ontology.org/?id=DOID:12935 DOID:12935]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.238.057 C14.280.238.057]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.775.100.087.250 C25.775.100.087.250]

|

|

|-

| alcoholic gastritis

| class of disease

| gastritis
long-term effects of alcohol consumption
chronic gastritis

| human disease

| [http://www.disease-ontology.org/?id=DOID:8680 DOID:8680]

|

|

|

|-

| alcoholic hepatitis

| class of disease

| hepatitis
alcoholic liver disease
disease

| hepatitis (inflammation of the liver) due to excessive intake of alcohol

| [http://www.disease-ontology.org/?id=DOID:12351 DOID:12351]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.380.290 C06.552.380.290]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.645.490 C06.552.645.490]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.775.100.087.645.490 C25.775.100.087.645.490]

| Alcoholic hepatitis

| File:Mallory body high mag cropped.jpg

|-

| alcoholic liver cirrhosis

| class of disease

| liver cirrhosis
alcoholic liver disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14018 DOID:14018]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.630.380 C06.552.630.380]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.645.590 C06.552.645.590]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.775.100.087.645.550 C25.775.100.087.645.550]

| Alcoholic cirrhosis

|

|-

| alcoholic neuropathy

| class of disease

| inflammatory and toxic neuropathy
polyneuropathy
long-term effects of alcohol consumption
nervous system alcohol-induced disorders
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14183 DOID:14183]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.800.050 C10.668.829.800.050]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.720.112.400 C10.720.112.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.723.705.150.400 C25.723.705.150.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.775.100.087.193.400 C25.775.100.087.193.400]

|

|

|-

| alcoholic pancreatitis

| class of disease

| pancreatitis
long-term effects of alcohol consumption
alcohol and health

| human disease

| [http://www.disease-ontology.org/?id=DOID:4988 DOID:4988]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.689.750.660 C06.689.750.660]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.775.100.087.730 C25.775.100.087.730]

|

|

|-

| alcuronium bromide allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger alcuronium bromide

| [http://www.disease-ontology.org/?id=DOID:0040077 DOID:0040077]

|

|

|

|-

| aleukemic leukemia

| class of disease

| leukemia

| leukemia that arises from changes in the tissues forming white blood cells and characterized by a normal or decreased number of white blood cells in the circulating blood

| [http://www.disease-ontology.org/?id=DOID:6004 DOID:6004]

|

|

|

|-

| aleukemic leukemia cutis

| class of disease

| aleukemic leukemia
Leukemia cutis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6003 DOID:6003]

|

|

|

|-

| aleukemic monocytic leukemia cutis

| class of disease

| aleukemic leukemia cutis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6958 DOID:6958]

|

|

|

|-

| alexithymia

| class of disease

| agnosia
disease

| subclinical deficiency in understanding, processing, or describing emotions

| [http://www.disease-ontology.org/?id=DOID:0060131 DOID:0060131]

|

|

| File:Autism Aspect Alexithymia 1.png

|-

| algoneurodystrophy

| class of disease

| complex regional pain syndrome

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14022 DOID:14022]

|

|

|

|-

| allergic asthma

| class of disease

| respiratory allergy
asthma
extrinsic asthma

| asthma with a basis in a pathological type I hypersensitivity reaction

| [http://www.disease-ontology.org/?id=DOID:9415 DOID:9415]

|

| Asthma

|

|-

| allergic conjunctivitis

| class of disease
symptom or sign

| chronic conjunctivitis
eye allergy
allergy

| chronic conjunctivitis that is an inflammation of the conjunctiva

| [http://www.disease-ontology.org/?id=DOID:11204 DOID:11204]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.187.183.200 C11.187.183.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.200 C20.543.480.200]

| Allergic conjunctivitis

| File:Allergicconjunctivitis.jpg

|-

| allergic contact dermatitis

| class of disease

| allergic dermatitis
contact dermatitis
disease

| medical condition

| [http://www.disease-ontology.org/?id=DOID:3042 DOID:3042]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.174.255.100 C17.800.174.255.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.815.255.100 C17.800.815.255.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.418.150 C20.543.418.150]

| Allergic contact dermatitis

|

|-

| allergic contact dermatitis of eyelid

| class of disease

| noninfectious dermatoses of eyelid
allergic contact dermatitis
Eyelid dermatitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1895 DOID:1895]

|

|

|

|-

| allergic rhinitis

| class of disease
symptom or sign

| rhinitis
respiratory allergy
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:4481 DOID:4481]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.460.799.315 C08.460.799.315]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.674.453 C08.674.453]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.603.799.315 C09.603.799.315]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.680.443 C20.543.480.680.443]

| Allergic rhinitis

| File:Misc pollen colorized.jpg

|-

| allescheriosis

| class of disease

| primary systemic mycosis
Pseudallescheriasis

| primary systemic mycosis that results in systemic fungal infection, has material basis in Pseudallescheria boydii, which results in formation of abscesses

| [http://www.disease-ontology.org/?id=DOID:11186 DOID:11186]

|

|

|

|-

| alopecia areata

| class of disease
symptom or sign

| alopecia
autoimmune disease
autoimmune skin disease

| condition in which hair is lost from some or all areas of the body

| [http://www.disease-ontology.org/?id=DOID:986 DOID:986]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.329.937.122.147 C17.800.329.937.122.147]

| Alopecia areata

| File:Allopecia areata.JPG

|-

| alopecia-intellectual disability syndrome

| class of disease

| genetic syndromic intellectual disability
syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080627 DOID:0080627]

|

|

|

|-

| alopecia-mental retardation syndrome 1

| class of disease

| autosomal recessive disease
alopecia-intellectual disability syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080628 DOID:0080628]

|

|

|

|-

| alopecia-mental retardation syndrome 2

| class of disease

| alopecia-intellectual disability syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080629 DOID:0080629]

|

|

|

|-

| alopecia-mental retardation syndrome 4

| class of disease

| alopecia-intellectual disability syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080950 DOID:0080950]

|

|

|

|-

| alpha chain disease

| class of disease

| heavy chain disease
intestinal neoplasm

| heavy chain disease that results from an overproduction of alpha antibodies (IgA)

| [http://www.disease-ontology.org/?id=DOID:0060126 DOID:0060126]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386.390 C04.557.386.390]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.371.411.512 C06.301.371.411.512]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.249.411.512 C06.405.249.411.512]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.491.505 C06.405.469.491.505]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.147.780.490.512 C15.378.147.780.490.512]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.435.512 C15.604.515.435.512]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.512 C20.683.515.512]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.780.490.512 C20.683.780.490.512]

|

|

|-

| alpha-thalassemia-myelodysplastic syndrome

| class of disease

| Acquired hemolytic anemia
alpha-thalassemia-related diseases
myelodysplastic syndrome
syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112125 DOID:0112125]

|

|

|

|-

| alternating esotropia

| class of disease

| esotropia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9888 DOID:9888]

|

|

|

|-

| alternating exotropia

| class of disease

| exotropia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1142 DOID:1142]

|

|

|

|-

| alveolar osteitis

| class of disease

| periostitis
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:13585 DOID:13585]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.227 C07.465.227]

|

|

|-

| alveolar rhabdomyosarcoma

| class of disease

| rhabdomyosarcoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:4051 DOID:4051]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.590.550.660.665 C04.557.450.590.550.660.665]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.550.660.665 C04.557.450.795.550.660.665]

|

|

|-

| alveoli adenoma

| class of disease

| lung adenoma
bronchial neoplasm
benign neoplasms by histologic type
adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8003 DOID:8003]

|

| Alveolar adenoma

|

|-

| amblyopia

| class of disease
symptom or sign

| eye disease
visual impairment
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:10376 DOID:10376]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.055 C10.228.140.055]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.751.941.073 C10.597.751.941.073]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.966.073 C11.966.073]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.763.941.073 C23.888.592.763.941.073]

| Amblyopia

| File:Child eyepatch.jpg

|-

| amelanotic melanoma

| class of disease

| melanoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:4359 DOID:4359]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.650.510.515 C04.557.465.625.650.510.515]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.650.510.515 C04.557.580.625.650.510.515]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.665.510.515 C04.557.665.510.515]

|

|

|-

| amelogenesis imperfecta type 1B

| class of disease

| amelogenesis imperfecta
autosomal dominant disease

| amelogenesis imperfecta that has material basis in heterozygous mutation in the enamelin gene (ENAM) on chromosome 4q13

| [http://www.disease-ontology.org/?id=DOID:0110052 DOID:0110052]

|

|

|

|-

| amelogenesis imperfecta type 2A6

| class of disease

| amelogenesis imperfecta

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080960 DOID:0080960]

|

|

|

|-

| amelogenesis imperfecta type 3B

| class of disease

| amelogenesis imperfecta
autosomal dominant disease
amelogenesis imperfecta type 3

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080243 DOID:0080243]

|

|

|

|-

| amelogenesis imperfecta type 3C

| class of disease

| amelogenesis imperfecta type 3
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111722 DOID:0111722]

|

|

|

|-

| amenorrhea

| class of disease

| female reproductive system disease
hypomenorrhea
disease

| absence of a menstrual period in a woman of reproductive age

| [http://www.disease-ontology.org/?id=DOID:13938 DOID:13938]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.568.500 C23.550.568.500]

|

|

|-

| ametropic amblyopia

| class of disease

| amblyopia
refractive error

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10377 DOID:10377]

|

|

|

|-

| amino acid metabolic disorder

| class of disease

| inherited metabolic disorder

| inherited metabolic disorder that is characterized by impaired synthesis and degradation of amino acids

| [http://www.disease-ontology.org/?id=DOID:9252 DOID:9252]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.100 C16.320.565.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.100 C18.452.648.100]

|

|

|-

| amnesia

| class of disease
symptom or sign

| cognitive disorder
memory disorder
psychopathological syndrome
disease

| cognitive disorder where the memory is disturbed or lost and involves the loss of memories previously established, loss of the ability to create new memories, continuous high blood pressure and severe shock may also cause amnesia

| [http://www.disease-ontology.org/?id=DOID:10914 DOID:10914]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.606.525.100 C10.597.606.525.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.604.529.100 C23.888.592.604.529.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F01.700.625.100 F01.700.625.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.615.200 F03.615.200]

|

| File:Amnesie.jpg

|-

| amodiaquine allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger amodiaquine

| [http://www.disease-ontology.org/?id=DOID:0040022 DOID:0040022]

|

|

|

|-

| amoxicillin allergy

| class of disease

| beta-lactam allergy

| beta-lactam allergy that has allergic trigger amoxicillin

| [http://www.disease-ontology.org/?id=DOID:0040004 DOID:0040004]

|

|

|

|-

| amphetamine-related disorders

| class of disease

| substance abuse
stimulant use disorder

| negative health consequences of substance abuse that involves the recurring use of amphetamines

| [http://www.disease-ontology.org/?id=DOID:670 DOID:670]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.775.225 C25.775.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.900.225 F03.900.225]

|

|

|-

| ampulla of Vater adenocarcinoma

| class of disease

| ampulla of Vater carcinoma
duodenum adenocarcinoma
extrahepatic bile duct adenocarcinoma
adenocarcinoma

| ampulla of Vater carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:3502 DOID:3502]

|

|

|

|-

| ampulla of Vater adenosquamous carcinoma

| class of disease

| ampulla of Vater squamous cell carcinoma
adenosquamous bile duct carcinoma
squamous cell carcinoma
ampulla of Vater cancer

| ampulla of Vater carcinoma that derives from squamous cells and gland-like cells

| [http://www.disease-ontology.org/?id=DOID:5628 DOID:5628]

|

|

|

|-

| ampulla of Vater cancer

| class of disease

| duodenum cancer
ampulla of Vater neoplasm
bile duct cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10020 DOID:10020]

|

|

|

|-

| ampulla of Vater carcinoma

| class of disease

| ampulla of Vater cancer
small intestine carcinoma
duodenum cancer
extrahepatic bile duct carcinoma
carcinoma

| ampulla of Vater cancer that has material basis in abnormally proliferating cells derives from epithelial cells

| [http://www.disease-ontology.org/?id=DOID:4932 DOID:4932]

|

| Carcinoma of the ampulla of Vater

|

|-

| ampulla of Vater clear cell adenocarcinoma

| class of disease

| ampulla of Vater adenocarcinoma
bile duct clear cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5308 DOID:5308]

|

|

|

|-

| ampulla of Vater mucinous adenocarcinoma

| class of disease

| ampulla of Vater adenocarcinoma
bile duct mucinous adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3693 DOID:3693]

|

|

|

|-

| ampulla of Vater neoplasm

| class of disease

| duodenal neoplasm
bile duct disease
biliary tract neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10022 DOID:10022]

|

|

|

|-

| ampulla of Vater small cell carcinoma

| class of disease

| ampulla of Vater carcinoma
liver neuroendocrine carcinoma
small cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7136 DOID:7136]

|

|

|

|-

| ampulla of Vater squamous cell carcinoma

| class of disease

| ampulla of Vater carcinoma
squamous cell bile duct carcinoma
squamous cell carcinoma of the small intestine
squamous cell carcinoma

| ampulla of Vater carcinoma that derives from epithelial squamous cells

| [http://www.disease-ontology.org/?id=DOID:5527 DOID:5527]

|

|

|

|-

| ampullary signet ring cell adenocarcinoma

| class of disease

| ampulla of Vater adenocarcinoma
bile duct signet ring cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3501 DOID:3501]

|

|

|

|-

| amusia

| class of disease

| agnosia
auditory agnosia
music-specific disorders

| loss of the ability to recognize musical notes, rhythms, and intervals

| [http://www.disease-ontology.org/?id=DOID:0060132 DOID:0060132]

|

|

|

|-

| amyloid tumor

| class of disease

| mesenchymal cell neoplasm
connective tissue benign neoplasm
amyloidosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6755 DOID:6755]

|

|

|

|-

| amyloidosis

| class of disease

| systemic disease
proteostasis deficiency
acquired metabolic disease
disease

| metabolic disease involving abnormal deposited amyloid proteins

| [http://www.disease-ontology.org/?id=DOID:9120 DOID:9120]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.845.500 C18.452.845.500]

| Amyloidosis

| File:Small bowel duodenum with amyloid deposition congo red 10X.jpg

|-

| amyotrohpic lateral sclerosis type 22

| class of disease

| amyotrophic lateral sclerosis

| amyotrophic lateral sclerosis that has material basis in mutation in the TUBA4A gene on chromosome 2q35

| [http://www.disease-ontology.org/?id=DOID:0060355 DOID:0060355]

|

|

|

|-

| amyotrophic lateral sclerosis type 1

| class of disease

| amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis

| The most common type of familial ALS that has material basis in mutation in the SOD1 gene on chromosome 21

| [http://www.disease-ontology.org/?id=DOID:0060193 DOID:0060193]

|

|

|

|-

| amyotrophic lateral sclerosis type 10

| class of disease

| amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis
amyotrophic lateral sclerosis and frontotemporal dementia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060201 DOID:0060201]

|

|

|

|-

| amyotrophic lateral sclerosis type 11

| class of disease

| amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060202 DOID:0060202]

|

|

|

|-

| amyotrophic lateral sclerosis type 12

| class of disease

| amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis

| amyotrophic lateral sclerosis that has material basis in mutation in the OPTN gene on chromosome 10

| [http://www.disease-ontology.org/?id=DOID:0060203 DOID:0060203]

|

|

|

|-

| amyotrophic lateral sclerosis type 13

| class of disease

| amyotrophic lateral sclerosis

| amyotrophic lateral sclerosis where a mutation that has material basis in the ATXN2 gene on chromosome 12 contributes to suscepitbility

| [http://www.disease-ontology.org/?id=DOID:0060204 DOID:0060204]

|

|

|

|-

| amyotrophic lateral sclerosis type 14

| class of disease

| amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis
amyotrophic lateral sclerosis and frontotemporal dementia

| amyotrophic lateral sclerosis that has material basis in mutation in the VCP gene on chromosome 9

| [http://www.disease-ontology.org/?id=DOID:0060205 DOID:0060205]

|

|

|

|-

| amyotrophic lateral sclerosis type 15

| class of disease

| amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis

| amyotrophic lateral sclerosis that has material basis in mutation in the UBQLN2 gene on chromosome X

| [http://www.disease-ontology.org/?id=DOID:0060206 DOID:0060206]

|

|

|

|-

| amyotrophic lateral sclerosis type 18

| class of disease

| amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis

| amyotrophic lateral sclerosis that has material basis in mutation in the PFN1 gene on chromosome 17

| [http://www.disease-ontology.org/?id=DOID:0060209 DOID:0060209]

|

|

|

|-

| amyotrophic lateral sclerosis type 19

| class of disease

| amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis

| amyotrophic lateral sclerosis that has material basis in mutation in the ERBB4 gene on chromosome 2

| [http://www.disease-ontology.org/?id=DOID:0060210 DOID:0060210]

|

|

|

|-

| amyotrophic lateral sclerosis type 2

| class of disease

| amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060194 DOID:0060194]

|

|

|

|-

| amyotrophic lateral sclerosis type 20

| class of disease

| amyotrophic lateral sclerosis
familial amyotrophic lateral sclerosis

| amyotrophic lateral sclerosis with juvenile onset that has material basis in mutation in the HNRNPA1 gene on chromosome 12

| [http://www.disease-ontology.org/?id=DOID:0060211 DOID:0060211]

|

|

|

|-

| amyotrophic lateral sclerosis type 21

| class of disease

| amyotrophic lateral sclerosis
nervous system heredodegenerative disease

| amyotrophic lateral sclerosis that has material basis in mutation in the MATR3 gene on chromosome 5

| [http://www.disease-ontology.org/?id=DOID:0060212 DOID:0060212]

|

|

|

|-

| amyotrophic lateral sclerosis type 23

| class of disease

| amyotrophic lateral sclerosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080225 DOID:0080225]

|

|

|

|-

| amyotrophic lateral sclerosis type 3

| class of disease

| amyotrophic lateral sclerosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060195 DOID:0060195]

|

|

|

|-

| amyotrophic lateral sclerosis type 6

| class of disease

| amyotrophic lateral sclerosis
sporadic amyotrophic lateral sclerosis
amyotrophic lateral sclerosis and frontotemporal dementia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060198 DOID:0060198]

|

|

|

|-

| amyotrophic lateral sclerosis type 7

| class of disease

| amyotrophic lateral sclerosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060199 DOID:0060199]

|

|

|

|-

| amyotrophic lateral sclerosis type 8

| class of disease

| amyotrophic lateral sclerosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050752 DOID:0050752]

|

|

|

|-

| amyotrophic lateral sclerosis type 9

| class of disease

| amyotrophic lateral sclerosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060200 DOID:0060200]

|

|

|

|-

| amyotrophic lateral sclerosis-parkinsonism/dementia complex 1

| class of disease

| neurodegeneration

| A neurodegenerative disease characterized by chronic, progressive amyotrophic lateral sclerosis and parkinsonism-dementia. Susceptibility to this disease is influenced by heterozygous mutation in TRPM7 on 15q21.2.

| [http://www.disease-ontology.org/?id=DOID:0111246 DOID:0111246]

|

|

|

|-

| amyotrophic neuralgia

| class of disease

| brachial plexus neuropathy
neurodegeneration

| human disease

| [http://www.disease-ontology.org/?id=DOID:10383 DOID:10383]

|

|

|

|-

| anaerobic meningitis

| class of disease

| bacterial meningitis
anaerobic infection

| human disease

| [http://www.disease-ontology.org/?id=DOID:14559 DOID:14559]

|

|

|

|-

| anal Buschke-Lowenstein tumor

| class of disease

| anal squamous cell carcinoma
verrucous carcinoma
giant condyloma acuminatum

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7175 DOID:7175]

|

|

|

|-

| anal Paget's disease

| class of disease

| anus adenocarcinoma
extramammary Paget's disease
rare genetic intestinal disease
inherited digestive tract tumor
rare epithelial tumor of rectum

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3446 DOID:3446]

|

| Anal Paget's disease

|

|-

| anal canal Paget's disease

| class of disease

| anal canal adenocarcinoma
extramammary Paget's disease
anal Paget's disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8119 DOID:8119]

|

|

|

|-

| anal canal adenocarcinoma

| class of disease

| anus adenocarcinoma
anal canal cancer
adenocarcinoma

| anal canal cancer that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:3692 DOID:3692]

|

|

|

|-

| anal canal cancer

| class of disease

| large intestine cancer

| large intestine cancer that is located in the terminal part of the large intestine

| [http://www.disease-ontology.org/?id=DOID:0050688 DOID:0050688]

|

|

|

|-

| anal canal carcinoma

| class of disease

| carcinoma
anal canal cancer

| anal canal cancer that derives from epithelial cells

| [http://www.disease-ontology.org/?id=DOID:6126 DOID:6126]

|

|

|

|-

| anal canal squamous cell carcinoma

| class of disease

| squamous cell carcinoma
anal squamous cell carcinoma
anal canal cancer

| anal canal cancer that derives from epithelial squamous cells

| [http://www.disease-ontology.org/?id=DOID:7177 DOID:7177]

|

|

|

|-

| anal cancer

| class of disease

| anus neoplasm
anal canal cancer
anal disease
large intestine cancer
disease

| Is a rare disease which it is caused in most of the cases by the infection of the Human Papilloma Virus (HPV).

| [http://www.disease-ontology.org/?id=DOID:14110 DOID:14110]

|

| Anal cancer

|

|-

| anal carcinoma

| class of disease

| anal cancer
carcinoma

| anus cancer that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the anus

| [http://www.disease-ontology.org/?id=DOID:4908 DOID:4908]

|

|

|

|-

| anal carcinoma in situ

| class of disease

| anal carcinoma
rectum carcinoma in situ
in situ carcinoma
Anal dysplasia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9087 DOID:9087]

|

|

|

|-

| anal colloid adenocarcinoma

| class of disease

| anus adenocarcinoma
rectum mucinous adenocarcinoma

| anus carcinoma that derives from epithelial cells of glandular origin located in the anal colloid

| [http://www.disease-ontology.org/?id=DOID:3691 DOID:3691]

|

|

|

|-

| anal disease

| class of disease

| anorectal disorder
rectal disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3128 DOID:3128]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.860.101 C06.405.469.860.101]

| Diseases and disorders of anus and anal canal

|

|-

| anal fistula

| class of disease

| rectal disease

| anus disease characterized by an abnormal connection between the epithelialised surface of the anal canal and the perianal skin

| [http://www.disease-ontology.org/?id=DOID:0060328 DOID:0060328]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.267.550.600 C06.267.550.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.471.600 C06.405.469.471.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.860.752 C06.405.469.860.752]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.300.575.185.550.600 C23.300.575.185.550.600]

| Anal fistula

|

|-

| anal gland adenocarcinoma

| class of disease

| anus adenocarcinoma

| anus carcinoma that derives from epithelial cells of glandular origin located in the anal gland

| [http://www.disease-ontology.org/?id=DOID:7531 DOID:7531]

|

|

|

|-

| anal margin basal cell carcinoma

| class of disease

| anal margin carcinoma
basal-cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4283 DOID:4283]

|

|

|

|-

| anal margin carcinoma

| class of disease

| anal carcinoma
skin carcinoma
skin cancer

| anal carcinoma that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the anal margin (where the canal meets the outside skin at the anus)

| [http://www.disease-ontology.org/?id=DOID:4284 DOID:4284]

|

|

|

|-

| anal margin squamous cell carcinoma

| class of disease

| anal margin carcinoma
squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12239 DOID:12239]

|

|

|

|-

| anal neuroendocrine tumor

| class of disease

| anus neoplasm
rectum neuroendocrine neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5545 DOID:5545]

|

|

|

|-

| anal spasm

| class of disease

| anal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11374 DOID:11374]

|

|

|

|-

| anal squamous cell carcinoma

| class of disease

| anal carcinoma
rectum squamous cell carcinoma
squamous cell carcinoma

| anal carcinoma that arises near the squamocolumnar junction

| [http://www.disease-ontology.org/?id=DOID:5525 DOID:5525]

|

|

|

|-

| anal stricture

| class of disease

| anorectal anomalies
anal disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:11014 DOID:11014]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.198.025 C06.198.025]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.314.047 C16.131.314.047]

|

|

|-

| anaplastic astrocytoma

| class of disease

| astrocytoma

| astrocytoma that is characterized by cells with regular, round to oval nuclei

| [http://www.disease-ontology.org/?id=DOID:3078 DOID:3078]

|

| Anaplastic astrocytoma

| File:405518-FIBRILLARY OR DIFFUSE ASTROCYTIC NEOPLASM.jpg

|-

| anaplastic ependymoma

| class of disease

| ependymoma
grade III glioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5889 DOID:5889]

|

| Anaplastic ependymoma

|

|-

| anaplastic large-cell lymphoma

| class of disease

| T-cell lymphoma
non-Hodgkin lymphoma

| non-Hodgkin lymphoma involving aberrant T-cells

| [http://www.disease-ontology.org/?id=DOID:0050744 DOID:0050744]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386.480.750.399 C04.557.386.480.750.399]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.569.480.750.600 C15.604.515.569.480.750.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.761.480.750.399 C20.683.515.761.480.750.399]

|

|

|-

| anaplastic oligodendroglioma

| class of disease

| oligodendroglioma

| human disease

| [http://www.disease-ontology.org/?id=DOID:7154 DOID:7154]

|

| Anaplastic oligodendroglioma

| File:Oligodendroglioma 003.jpg

|-

| anaplastic thyroid cancer

| class of disease

| thyroid cancer
large cell carcinoma
undifferentiated carcinoma
thyroid carcinoma

| form of thyroid cancer

| [http://www.disease-ontology.org/?id=DOID:0080522 DOID:0080522]

|

|

|

|-

| anatomical narrow angle borderline glaucoma

| class of disease

| borderline glaucoma
chronic closed-angle glaucoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13327 DOID:13327]

|

|

|

|-

| anauxetic dysplasia

| class of disease

| spondyloepimetaphyseal dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080942 DOID:0080942]

|

|

|

|-

| anauxetic dysplasia 2

| class of disease

| autosomal recessive disease
anauxetic dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080962 DOID:0080962]

|

|

|

|-

| androgen insensitivity syndrome

| class of disease

| pseudohermaphroditism
sex differentiation disease
disease

| sex differentiation condition involving hormonal resistance due to androgen receptor dysfunction in a karyotypically male person

| [http://www.disease-ontology.org/?id=DOID:4674 DOID:4674]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.706.316.096.500 C12.706.316.096.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.875.253.096.500 C13.351.875.253.096.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.316.096.500 C16.131.939.316.096.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.322.061 C16.320.322.061]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.119.096.500 C19.391.119.096.500]

| Androgen insensitivity syndrome

| File:Women with androgen insensitivity syndrome.jpg

|-

| androgenic alopecia

| class of disease

| baldness
androgen-dependent syndrome
disease

| hair loss due to susceptibility of hair follicles to androgenic miniaturization

| [http://www.disease-ontology.org/?id=DOID:0050801 DOID:0050801]

|

| Androgenic alopecia

| File:Male pattern baldness.jpg

|-

| anemia

| class of disease
symptom or sign

| hematopoietic system disease
cytopenia
hemic system symptom
disease

| decrease in number of red blood cells

| [http://www.disease-ontology.org/?id=DOID:2355 DOID:2355]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071 C15.378.071]

| Anemias

| File:AnemiaFrote.jpg

|-

| anemia of prematurity

| class of disease

| neonatal anemia
premature infant disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11243 DOID:11243]

|

|

|

|-

| anencephaly

| class of disease

| nervous system malformations
disease

| absence of a major portion of the brain, skull, and scalp that occurs during embryonic development

| [http://www.disease-ontology.org/?id=DOID:0060668 DOID:0060668]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.500.680.196 C10.500.680.196]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.085.197 C16.131.085.197]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.666.680.196 C16.131.666.680.196]

| Anencephaly

| File:Anencephaly-web.jpg

|-

| aneruptive fever

| class of disease

| spotted fever

| A spotted fever that has material basis in Rickettsia helvetica, which is transmitted by ticks (Ixodes sp). The infection has symptom fever, has symptom headache, has symptom myalgia.

| [http://www.disease-ontology.org/?id=DOID:0050484 DOID:0050484]

|

|

|

|-

| aneurysm of heart

| class of disease

| heart disease
aneurysm
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9768 DOID:9768]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.358 C14.280.358]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.055.608 C14.907.055.608]

| Heart aneurysms

|

|-

| aneurysm-osteoarthritis syndrome

| class of disease

| Loeys-Dietz syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070237 DOID:0070237]

|

|

|

|-

| angiodysplasia

| class of disease

| vascular disease
disease

| vascular disease that is characterized as a small vascular malformation of the gut

| [http://www.disease-ontology.org/?id=DOID:2494 DOID:2494]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.075 C14.907.075]

| Angiodysplasia

| File:Argon plasma coagulation.jpg

|-

| angiodysplasia of intestine

| class of disease

| intestinal disease
angiodysplasia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10846 DOID:10846]

|

|

|

|-

| angioid streaks

| class of disease

| retinal disease
rare genetic eye disease
genetic disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13401 DOID:13401]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.768.094 C11.768.094]

|

|

|-

| angioid streaks of choroid

| class of disease

| choroidal sclerosis
angioid streaks
nervous system heredodegenerative disease
genetic vascular disease
choroid disease
retinal degeneration

| angioid streaks that involves the optic choroid

| [http://www.disease-ontology.org/?id=DOID:979 DOID:979]

|

|

|

|-

| angioimmunoblastic T-cell lymphoma

| class of disease

| T-cell lymphoma
peripheral T-cell lymphoma
immunoblastic lymphadenopathy

| peripheral T-cell lymphoma characterized by autoimmune features and poor prognosis

| [http://www.disease-ontology.org/?id=DOID:0111147 DOID:0111147]

|

|

|

|-

| angiokeratoma

| class of disease

| skin hemangioma

| benign cutaneous lesion of capillaries, resulting in small marks of red to blue color and characterized by hyperkeratosis

| [http://www.disease-ontology.org/?id=DOID:479 DOID:479]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.645.115 C04.557.645.115]

| Angiokeratoma

| File:Angiokreatoma.jpg

|-

| angiokeratoma circumscriptum

| class of disease

| skin benign neoplasm
angiokeratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5949 DOID:5949]

|

|

|

|-

| angiokeratoma of Fordyce

| class of disease

| skin benign neoplasm
angiokeratoma
disease

| sebaceous glands that are present in most individuals

| [http://www.disease-ontology.org/?id=DOID:664 DOID:664]

|

| Fordyce's spots

|

|-

| angiokeratoma of Mibelli

| class of disease

| angiokeratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5948 DOID:5948]

|

|

|

|-

| angiolipoma

| class of disease

| lipoma

| lipoma that is a painful subcutaneous nodule, having all other features of a typical lipoma

| [http://www.disease-ontology.org/?id=DOID:3616 DOID:3616]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.550.100 C04.557.450.550.100]

| Angiolipoma

|

|-

| angioma serpiginosum

| class of disease

| skin hemangioma

| skin hemangioma characterized by the presence of small red dots that cluster together to form a linear or snake-like array or ring-shaped pattern located in the blood vessels of the skin

| [http://www.disease-ontology.org/?id=DOID:4028 DOID:4028]

|

|

|

|-

| angiomatous meningioma

| class of disease

| meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6548 DOID:6548]

|

|

|

|-

| angiomyolipoma

| class of disease

| benign neoplasms by histologic type
disease

| cell type benign neoplasm that from perivascular epithelioid cells

| [http://www.disease-ontology.org/?id=DOID:3314 DOID:3314]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.550.125 C04.557.450.550.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.692.249 C04.557.450.692.249]

| Angiomyolipomas

|

|-

| angiomyoma

| class of disease

| benign perivascular tumor
vascular disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4265 DOID:4265]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.590.450.125 C04.557.450.590.450.125]

|

|

|-

| angiosarcoma

| class of disease

| vascular tissue neoplasm
vascular cancer
disease

| malignant Vascular tumor that results in rapidly proliferating, extensively infiltrating anaplastic cells derives from blood vessels and derived from the lining of irregular blood-filled spaces

| [http://www.disease-ontology.org/?id=DOID:0001816 DOID:0001816]

|

| Angiosarcoma

| File:Angiosarcoma (5617087462).jpg

|-

| angle-closure glaucoma

| class of disease

| glaucoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:13550 DOID:13550]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.525.381.056 C11.525.381.056]

|

|

|-

| angular blepharoconjunctivitis

| class of disease

| blepharoconjunctivitis

| blepharoconjunctivitis that is characterized by fissuring, scaling, maceration and erythema of the lateral or medial canthal area

| [http://www.disease-ontology.org/?id=DOID:2455 DOID:2455]

|

|

|

|-

| angular cheilitis

| class of disease
symptom or sign

| cheilitis
disease

| cheilitis characterized by inflammation of one or both of the corners of the mouth

| [http://www.disease-ontology.org/?id=DOID:0060312 DOID:0060312]

|

| Angular cheilitis

| File:Angular Cheilitis.JPG

|-

| anhidrosis

| class of disease

| hypohidrosis
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11156 DOID:11156]

|

|

|

|-

| animal phobia

| class of disease

| specific phobia
disease

| specific phobia that involves a fear caused by the presence or thought of a specific animal that poses little or no danger at all

| [http://www.disease-ontology.org/?id=DOID:600 DOID:600]

|

|

|

|-

| aniseikonia

| class of disease

| refractive error
dysmetropsia
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050304 DOID:0050304]
[http://www.disease-ontology.org/?id=DOID:12274 DOID:12274]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.744.116 C11.744.116]

|

|

|-

| anismus

| class of disease
symptom or sign

| focal dystonia
constipation

| failure of the normal relaxation of pelvic floor muscles during attempted defecation

| [http://www.disease-ontology.org/?id=DOID:0050839 DOID:0050839]

|

|

|

|-

| anisometropia

| class of disease

| refractive error
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:12273 DOID:12273]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.744.126 C11.744.126]

|

|

|-

| ankyloglossia

| class of disease

| tongue disease
genetic nervous system disorder
genetic disease

| congenital disorder of tongue mobility

| [http://www.disease-ontology.org/?id=DOID:0060604 DOID:0060604]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.160 C07.160]

| Ankyloglossia

| File:Frenulum linguae.jpg

|-

| ankylosing spondylitis 1

| class of disease

| ankylosing spondylitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080603 DOID:0080603]

|

|

|

|-

| ankylosing spondylitis 2

| class of disease

| ankylosing spondylitis
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080604 DOID:0080604]

|

|

|

|-

| ankylosing spondylitis 3

| class of disease

| ankylosing spondylitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080605 DOID:0080605]

|

|

|

|-

| ankylosis

| class of disease

| arthropathy
joint stiffness
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:227 DOID:227]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.550.069 C05.550.069]

| Ankylosis

| File:Annual and analytical cyclopaedia of practical medicine (1898) (14803296453).jpg

|-

| anodontia

| class of disease

| tooth agenesis
tooth agenesis
tooth abnormality
tooth pathology
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:13714 DOID:13714]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.650.800.100 C07.650.800.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.793.700.100 C07.793.700.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.850.800.100 C16.131.850.800.100]

|

|

|-

| anomic aphasia

| class of disease
symptom or sign

| aphasia
clinical sign
disease

| type of aphasia

| [http://www.disease-ontology.org/?id=DOID:4541 DOID:4541]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.606.150.500.090 C10.597.606.150.500.090]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.604.150.500.090 C23.888.592.604.150.500.090]

|

|

|-

| anorexia nervosa

| class of disease

| eating disorder
disease

| type of eating disorder

| [http://www.disease-ontology.org/?id=DOID:8689 DOID:8689]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.400.128 F03.400.128]

| Anorexia nervosa

| File:Anorexia case 1900.jpg

|-

| anosognosia

| class of disease

| agnosia
disease

| Unawareness of one's own illness, symptoms or impairments

| [http://www.disease-ontology.org/?id=DOID:0060133 DOID:0060133]

|

|

|

|-

| anovulation

| class of disease

| ovarian disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3781 DOID:3781]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.056.630.050 C13.351.500.056.630.050]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.630.050 C19.391.630.050]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=G08.686.784.690.080 G08.686.784.690.080]

|

|

|-

| anterior cerebral artery infarction

| class of disease

| cerebral infarction
cerebral artery occlusion

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3528 DOID:3528]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.150.477.200.400 C10.228.140.300.150.477.200.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.510.200.325 C10.228.140.300.510.200.325]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.775.200.200.400 C10.228.140.300.775.200.200.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.092.477.200.400 C14.907.253.092.477.200.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.560.200.325 C14.907.253.560.200.325]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.855.200.200.400 C14.907.253.855.200.200.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.513.355.250.200.400 C23.550.513.355.250.200.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.717.489.250.200.400 C23.550.717.489.250.200.400]

|

|

|-

| anterior compartment syndrome

| class of disease

| compartment syndrome

| disease

| [http://www.disease-ontology.org/?id=DOID:3933 DOID:3933]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.180.063 C05.651.180.063]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.303.063 C14.907.303.063]

|

|

|-

| anterior corneal pigmentation

| class of disease

| corneal deposit

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12307 DOID:12307]

|

|

|

|-

| anterior dislocation of lens

| class of disease

| globe disease
lens subluxation

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2460 DOID:2460]

|

|

|

|-

| anterior horn cell disease

| class of disease

| spinal muscular atrophy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4873 DOID:4873]

|

|

|

|-

| anterior ischemic optic neuropathy

| class of disease

| ischemic optic neuropathy
optic nerve disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12010 DOID:12010]

|

|

|

|-

| anterior optic tract meningioma

| class of disease

| optic nerve tumor
visual pathway meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6334 DOID:6334]

|

|

|

|-

| anterior scleritis

| class of disease

| scleritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13794 DOID:13794]

|

|

|

|-

| anterior segment dysgenesis 1

| class of disease

| corneal opacification and other ocular anomalies
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080606 DOID:0080606]

|

|

|

|-

| anterior segment dysgenesis 2

| class of disease

| autosomal recessive disease
corneal opacification and other ocular anomalies

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080607 DOID:0080607]

|

|

|

|-

| anterior segment dysgenesis 3

| class of disease

| autosomal dominant disease
corneal opacification and other ocular anomalies

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080608 DOID:0080608]

|

|

|

|-

| anterior segment dysgenesis 4

| class of disease

| corneal opacification and other ocular anomalies
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080609 DOID:0080609]

|

|

|

|-

| anterior segment dysgenesis 5

| class of disease

| corneal opacification and other ocular anomalies

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080610 DOID:0080610]

|

|

|

|-

| anterior spinal artery syndrome

| class of disease

| syndrome
cerebrovascular disease
vascular myelopathy
artery disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6712 DOID:6712]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.854.785.650.100 C10.228.854.785.650.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.790.550.100 C14.907.790.550.100]

|

|

|-

| anterior urethral cancer

| class of disease

| urethral cancer
female urethral cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8272 DOID:8272]

|

|

|

|-

| anterior uveitis

| class of disease

| uveitis
panuveitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1407 DOID:1407]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.879.780.880 C11.941.879.780.880]

|

|

|-

| anterograde amnesia

| class of disease

| amnesia

| loss of the ability to create new memories after the onset of amnesia

| [http://www.disease-ontology.org/?id=DOID:5340 DOID:5340]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.606.525.100.075 C10.597.606.525.100.075]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.604.529.100.075 C23.888.592.604.529.100.075]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F01.700.625.100.075 F01.700.625.100.075]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.615.200.137 F03.615.200.137]

|

|

|-

| anterolateral myocardial infarction

| class of disease

| myocardial infarction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5845 DOID:5845]

|

|

|

|-

| anteroseptal myocardial infarction

| class of disease

| myocardial infarction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5855 DOID:5855]

|

|

|

|-

| anthracosilicosis

| class of disease

| pneumoconiosis
anthracosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:10324 DOID:10324]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.483.581.062.500 C08.381.483.581.062.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.483.581.760.125 C08.381.483.581.760.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.520.702.062.500 C08.381.520.702.062.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.520.702.760.125 C08.381.520.702.760.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C24.800.834.201 C24.800.834.201]

|

| File:Coal workers pneumocniosis - Anthracosilicosis 1.jpg

|-

| anthracosis

| class of disease

| occupational disease
pneumoconiosis
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:10327 DOID:10327]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.483.581.062 C08.381.483.581.062]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.520.702.062 C08.381.520.702.062]

| Black lung disease

| File:Anthracosis (4860889071).jpg

|-

| anti-basement membrane glomerulonephritis

| class of disease

| Goodpasture syndrome

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4780 DOID:4780]

|

|

|

|-

| antidepressant abuse

| class of disease

| substance abuse
abuse of medicaments

| substance abuse that involves the recurring use of antidepressant drugs despite negative consequences

| [http://www.disease-ontology.org/?id=DOID:11718 DOID:11718]

|

|

|

|-

| antisocial personality disorder

| class of disease

| Cluster B personality disorders
personality disorder
disease

| Personality disorder that involves a pervasive pattern of disregard for other people

| [http://www.disease-ontology.org/?id=DOID:10939 DOID:10939]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.675.050 F03.675.050]

| Antisocial personality disorder

|

|-

| antisynthetase syndrome

| class of disease

| autoimmune disease
idiopathic inflammatory myopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080744 DOID:0080744]

|

|

|

|-

| anuria

| class of disease
symptom or sign

| kidney disease
oliguria
urological symptom

| lack of urine

| [http://www.disease-ontology.org/?id=DOID:2983 DOID:2983]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.968.419.078 C12.050.351.968.419.078]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.777.934.141 C12.200.777.934.141]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.777.419.078 C12.200.777.419.078]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.968.934.070 C12.050.351.968.934.070]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.950.419.078 C12.950.419.078]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.950.934.070 C12.950.934.070]

|

|

|-

| anus adenocarcinoma

| class of disease

| anal carcinoma
adenocarcinoma

| anal carcinoma that originating in the cortex of the adrenal gland and derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:3447 DOID:3447]

|

|

|

|-

| anus basaloid carcinoma

| class of disease

| anal squamous cell carcinoma
basaloid squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7174 DOID:7174]

|

|

|

|-

| anus leiomyoma

| class of disease

| leiomyoma
benign neoplasm of anus
rectum leiomyoma
anus neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5134 DOID:5134]

|

|

|

|-

| anus leiomyosarcoma

| class of disease

| anus sarcoma
leiomyosarcoma
rectum leiomyosarcoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:5267 DOID:5267]

|

|

|

|-

| anus lymphoma

| class of disease

| anal cancer
lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14139 DOID:14139]

|

|

|

|-

| anus neoplasm

| class of disease

| intestinal neoplasm
anal disease
intestinal benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4551 DOID:4551]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.476.411.307.790.040 C04.588.274.476.411.307.790.040]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.371.411.307.790.040 C06.301.371.411.307.790.040]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.249.411.307.790.040 C06.405.249.411.307.790.040]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.491.307.790.040 C06.405.469.491.307.790.040]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.860.101.163 C06.405.469.860.101.163]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.860.180.500.040 C06.405.469.860.180.500.040]

|

|

|-

| anus rhabdomyosarcoma

| class of disease

| anus sarcoma
rhabdomyosarcoma
rectum rhabdomyosarcoma
anal cancer

| rhabdomyosarcoma and sarcoma of the anus that is located in the anus

| [http://www.disease-ontology.org/?id=DOID:4066 DOID:4066]

|

|

|

|-

| anus sarcoma

| class of disease

| anal cancer
sarcoma
intestinal benign neoplasm

| sarcoma and malignant neoplasm of anus that is located in the anus

| [http://www.disease-ontology.org/?id=DOID:4067 DOID:4067]

|

|

|

|-

| anxiety disorder

| class of disease

| cognitive disorder
disease

| cognitive disorder with an excessive, irrational dread of everyday situations

| [http://www.disease-ontology.org/?id=DOID:2030 DOID:2030]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.080 F03.080]

| Anxiety disorders

|

|-

| aorta angiosarcoma

| class of disease

| angiosarcoma
aortic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:4510 DOID:4510]

|

|

|

|-

| aorta atresia

| class of disease

| aortic disease

| aortic disease that is characterized by an absence of an opening from the left ventricle of the heart into the aorta

| [http://www.disease-ontology.org/?id=DOID:14037 DOID:14037]

|

|

|

|-

| aortic aneurysm

| class of disease

| aortic disease
aneurysm
clinical sign
disease

| aorta to greater than 1.5 times normal size

| [http://www.disease-ontology.org/?id=DOID:3627 DOID:3627]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.055.239 C14.907.055.239]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.109.139 C14.907.109.139]

| Aortic aneurysms

|

|-

| aortic atherosclerosis

| class of disease

| atherosclerosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10230 DOID:10230]

|

|

|

|-

| aortic disease

| class of disease

| artery disease

| artery disease characterized by degeneration of the cells composing the aortic wall

| [http://www.disease-ontology.org/?id=DOID:520 DOID:520]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.109 C14.907.109]

|

|

|-

| aortic malignant tumor

| class of disease

| vascular cancer
aortic disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8352 DOID:8352]

|

|

|

|-

| aortic valve disease

| class of disease

| heart valve disease
aortic disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:62 DOID:62]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.484.048 C14.280.484.048]

| Aortic valve diseases

|

|-

| aortic valve disease 1

| class of disease

| familial bicuspid aortic valve

| bicuspid aortic valve disease that has material basis in heterozygous mutation in the NOTCH1 gene on chromosome 9q34

| [http://www.disease-ontology.org/?id=DOID:0080333 DOID:0080333]

|

|

|

|-

| aortic valve disease 2

| class of disease

| familial bicuspid aortic valve
autosomal dominant disease

| bicuspid aortic valve disease that has material basis in heterozygous mutation in the SMAD6 gene on chromosome 15q22

| [http://www.disease-ontology.org/?id=DOID:0080334 DOID:0080334]

|

|

|

|-

| aortic valve insufficiency

| class of disease

| aortic valve disease
valve insufficiency
disease

| aortic valve disease that is characterized by leaking of the aortic valve of the heart causes blood to flow in the reverse direction during ventricular diastole, from the aorta into the left ventricle

| [http://www.disease-ontology.org/?id=DOID:57 DOID:57]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.484.095 C14.280.484.095]

| Aortic valve insufficiency

| File:Myxomatous aortic valve.jpg

|-

| aortic valve prolapse

| class of disease

| aortic valve disease
heart valve prolapse

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5232 DOID:5232]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.484.400.100 C14.280.484.400.100]

|

|

|-

| aortitis

| class of disease

| aortic disease

| inflammation of the aortic wall

| [http://www.disease-ontology.org/?id=DOID:519 DOID:519]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.109.320 C14.907.109.320]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.940.080 C14.907.940.080]

| Aortitis

|

|-

| aphasia

| class of disease
symptom or sign

| language disorder
neurological symptom
specific language impairment-5
disease

| Inability to spoke

| [http://www.disease-ontology.org/?id=DOID:0060046 DOID:0060046]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.606.150.500.800.100 C10.597.606.150.500.800.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.604.150.500.800.100 C23.888.592.604.150.500.800.100]

| Aphasia

|

|-

| aphthous stomatitis

| class of disease
symptom or sign

| clinical sign
stomatitis
lesions in mouth
disease

| stomatitis characterized by the repeated formation of benign and non-contagious mouth ulcers

| [http://www.disease-ontology.org/?id=DOID:9663 DOID:9663]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.864.750 C07.465.864.750]

| Aphthous ulcer

| File:Aphthe Unterlippe.jpg

|-

| apical granuloma

| class of disease

| disease
periapical periodontitis
granuloma

| tooth disease

| [http://www.disease-ontology.org/?id=DOID:4617 DOID:4617]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.320.830.700.740 C07.320.830.700.740]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.306.700.740 C07.465.714.306.700.740]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.533.487.740 C07.465.714.533.487.740]

|

|

|-

| apical myocardial infarction

| class of disease

| myocardial infarction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5848 DOID:5848]

|

|

|

|-

| apocrine adenocarcinoma

| class of disease

| apocrine sweat gland cancer
sweat gland carcinoma
adenocarcinoma
Apocrine gland carcinoma

| apocrine sweat gland cancer that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:4933 DOID:4933]

|

|

|

|-

| apocrine adenoma

| class of disease

| apocrine sweat gland neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3895 DOID:3895]

|

|

|

|-

| apocrine adenosis of breast

| class of disease

| non-proliferative fibrocystic change of the breast

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5999 DOID:5999]

|

|

|

|-

| apocrine sweat gland cancer

| class of disease

| sweat gland cancer
apocrine sweat gland neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4934 DOID:4934]

|

|

|

|-

| apocrine sweat gland neoplasm

| class of disease

| sweat gland neoplasm
apocrine sweat gland disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5876 DOID:5876]

|

|

|

|-

| apolipoprotein C-3 deficiency

| class of disease

| cholesterol-ester transfer protein deficiency
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111370 DOID:0111370]

|

|

|

|-

| appendiceal neoplasm

| class of disease

| intestinal neoplasm
appendix disease
cecal neoplasm
intestinal benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11240 DOID:11240]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.476.411.184.290 C04.588.274.476.411.184.290]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.371.411.184.290 C06.301.371.411.184.290]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.249.411.184.290 C06.405.249.411.184.290]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.110.417.290 C06.405.469.110.417.290]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.491.184.290 C06.405.469.491.184.290]

| Appendiceal neoplasms

|

|-

| appendix cancer

| class of disease

| intestinal cancer
appendiceal neoplasm
appendix disease

| cancer that is located in the appendix

| [http://www.disease-ontology.org/?id=DOID:11239 DOID:11239]

|

| Appendiceal cancer

|

|-

| appendix disease

| class of disease

| gastrointestinal system disease
cecal disease

| gastrointestinal system disease that is located in the appendix

| [http://www.disease-ontology.org/?id=DOID:60000 DOID:60000]

|

| Diseases and disorders of appendix

|

|-

| appendix lymphoma

| class of disease

| appendix cancer
primary organ-specific lymphoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:11241 DOID:11241]

|

|

|

|-

| apperceptive agnosia

| class of disease

| visual agnosia
agnosia

| agnosia that is a loss of the ability to distinguish visual shapes

| [http://www.disease-ontology.org/?id=DOID:0060134 DOID:0060134]

|

|

|

|-

| apple allergy

| class of disease

| fruit allergy

| fruit allergy triggered by Malus domestica plant fruit food product.

| [http://www.disease-ontology.org/?id=DOID:0060504 DOID:0060504]

|

|

|

|-

| apricot allergy

| class of disease

| fruit allergy

| fruit allergy triggered by Prunus armeniaca plant fruit food product.

| [http://www.disease-ontology.org/?id=DOID:0060505 DOID:0060505]

|

|

|

|-

| aqueous misdirection

| class of disease

| glaucoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11149 DOID:11149]

|

|

|

|-

| arcus senilis

| class of disease

| corneal degeneration
rare genetic eye disease
genetic disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11342 DOID:11342]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.204.299.070 C11.204.299.070]

| Arcus senilis

| File:Four representative slides of corneal arcus.jpg

|-

| ariboflavinosis

| class of disease

| nutritional deficiency disease
vitamin deficiency
vitamin B deficiency
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8454 DOID:8454]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.654.521.500.133.699.713 C18.654.521.500.133.699.713]

|

| File:Angular Cheilitis.JPG

|-

| arrhythmogenic right ventricular dysplasia 1

| class of disease

| arrhythmogenic right ventricular cardiomyopathy
autosomal dominant disease

| arrhythmogenic right ventricular dysplasia that has material basis in heterozygous mutation in the TGFB3 gene on chromosome 14q24

| [http://www.disease-ontology.org/?id=DOID:0110070 DOID:0110070]

|

|

|

|-

| arrhythmogenic right ventricular dysplasia 3

| class of disease

| arrhythmogenic right ventricular cardiomyopathy
autosomal dominant disease

| arrhythmogenic right ventricular dysplasia associated with variation in the region 14q12-q22

| [http://www.disease-ontology.org/?id=DOID:0110072 DOID:0110072]

|

|

|

|-

| arrhythmogenic right ventricular dysplasia 4

| class of disease

| arrhythmogenic right ventricular cardiomyopathy
autosomal dominant disease

| An arrhythmogenic right ventricular dysplasia associated with variation in the region 2q32.1-q32.3.

| [http://www.disease-ontology.org/?id=DOID:0110073 DOID:0110073]

|

|

|

|-

| arrhythmogenic right ventricular dysplasia 6

| class of disease

| arrhythmogenic right ventricular cardiomyopathy

| arrhythmogenic right ventricular dysplasia associated with variation in the region 10p14-p12

| [http://www.disease-ontology.org/?id=DOID:0110075 DOID:0110075]

|

|

|

|-

| arterial hypertension

| class of disease
symptom or sign

| vascular disease
artery disease
clinical sign
hypertension
disease

| long term medical condition with elevated arterial blood pressure

| [http://www.disease-ontology.org/?id=DOID:10763 DOID:10763]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.489 C14.907.489]

| Hypertension

| File:Grade 1 hypertension.jpg

|-

| arteriolosclerosis

| class of disease

| arteriosclerosis
coronary artery disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5162 DOID:5162]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.137.126.056 C14.907.137.126.056]

| Arteriolosclerosis

|

|-

| arteriosclerosis

| class of disease

| artery disease
disease

| thickening, hardening and loss of elasticity of the walls of arteries

| [http://www.disease-ontology.org/?id=DOID:2349 DOID:2349]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.137.126 C14.907.137.126]

| Atherosclerosis

| File:Atherosclerosis, aorta, gross pathology PHIL 846 lores.jpg

|-

| arteriosclerosis obliterans

| class of disease

| arteriosclerosis
peripheral artery disease
coronary artery disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:5160 DOID:5160]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.137.126.114 C14.907.137.126.114]

|

|

|-

| arteriosclerotic cardiovascular disease

| class of disease

| arteriosclerosis
coronary artery disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:2348 DOID:2348]

|

|

|

|-

| arteritic anterior ischemic optic neuropathy

| class of disease

| anterior ischemic optic neuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050863 DOID:0050863]

|

|

|

|-

| artery disease

| class of disease

| vascular disease

| type of vascular disease

| [http://www.disease-ontology.org/?id=DOID:0050828 DOID:0050828]

|

|

|

|-

| arthrogryposis multiplex congenita-4

| class of disease

| autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080980 DOID:0080980]

|

|

|

|-

| arthrogryposis, renal dysfunction, and cholestasis 1

| class of disease

| arthrogryposis–renal dysfunction–cholestasis syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111353 DOID:0111353]

|

|

|

|-

| arthrogryposis, renal dysfunction, and cholestasis 2

| class of disease

| arthrogryposis–renal dysfunction–cholestasis syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111354 DOID:0111354]

|

|

|

|-

| arthropathy

| class of disease

| joint disorder
bone disease
disease

| disease of a joint

| [http://www.disease-ontology.org/?id=DOID:381 DOID:381]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.550 C05.550]

| Arthropathies

|

|-

| arthus reaction

| class of disease

| type III hypersensitivity

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1556 DOID:1556]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.520.100 C20.543.520.100]

|

|

|-

| articulation disorder

| class of disease

| speech disorder
language disorder

| speech disorder that involves mispronouncing speech sounds by omitting, distorting, substituting, or adding sounds which can make speech difficult to understand

| [http://www.disease-ontology.org/?id=DOID:4186 DOID:4186]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.606.150.500.800.150 C10.597.606.150.500.800.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.604.150.500.800.150 C23.888.592.604.150.500.800.150]

|

|

|-

| asbestos-related lung carcinoma

| class of disease

| lung carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7596 DOID:7596]

|

|

|

|-

| asbestosis

| class of disease

| pneumoconiosis
asbestos-related disease
disease

| pneumoconiosis caused by inhalation and retention of asbestos fibers

| [http://www.disease-ontology.org/?id=DOID:10320 DOID:10320]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.483.581.125 C08.381.483.581.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.520.702.125 C08.381.520.702.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C24.800.127 C24.800.127]

| Asbestosis

| File:Early Asbestosis in a Retired Pipe Fitter.jpg

|-

| ascending cholangitis

| class of disease
symptom or sign

| non-neoplastic bile duct disorder
inflammatory disease
bile duct disease
disease

| bile duct disease that is an inflammation of the bile duct

| [http://www.disease-ontology.org/?id=DOID:9446 DOID:9446]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.120.200 C06.130.120.200]

| Ascending cholangitis

| File:Cholangitis.jpg

|-

| ascending cholangitis

| class of disease

| ascending cholangitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14270 DOID:14270]

|

|

|

|-

| ascending colon cancer

| class of disease

| plump cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:218 DOID:218]

|

|

|

|-

| aseptic meningitis

| class of disease

| meningitis
non-infectious meningitis
disease

| meningitis caused by anything other than bacteria

| [http://www.disease-ontology.org/?id=DOID:12157 DOID:12157]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.586.625.220 C10.586.625.220]

|

|

|-

| aspergillosis

| class of disease

| opportunistic mycosis
disease

| infectious disease of humans, birds and other animals

| [http://www.disease-ontology.org/?id=DOID:13564 DOID:13564]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.703.080 C01.150.703.080]

| Aspergillosis

| File:Pulmonary aspergillosis (1) invasive type.jpg

|-

| asphyxia neonatorum

| class of disease

| respiratory disease
perinatal respiratory disorder
disease

| Respiratory failure in the newborn. (Dorland, 27th ed)

| [http://www.disease-ontology.org/?id=DOID:11088 DOID:11088]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.614.092 C16.614.092]

|

|

|-

| asphyxiating thoracic dysplasia

| class of disease

| osteochondrodysplasia
autosomal recessive disease
bone development disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050592 DOID:0050592]

|

| Asphyxiating thoracic dysplasia

|

|-

| asphyxiating thoracic dystrophy 1

| class of disease

| asphyxiating thoracic dysplasia
autosomal recessive disease

| asphyxiating thoracic dystrophy associated with variation in the region 15q13

| [http://www.disease-ontology.org/?id=DOID:0110085 DOID:0110085]

|

|

|

|-

| aspiration pneumonia

| class of disease
symptom or sign

| bacterial pneumonia
disease

| bronchopneumonia that develops due to the entrance of foreign materials into the lungs

| [http://www.disease-ontology.org/?id=DOID:0050152 DOID:0050152]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.677.529 C08.381.677.529]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.730.610.529 C08.730.610.529]

| Aspiration pneumonia

| File:Aspiration pneumonia (4861515094).jpg

|-

| aspiration pneumonitis

| class of disease

| pneumonia
aspiration pneumonia
disease

| chemical pneumonitis or aspiration pneumonitis caused by aspiration during anaesthesia, especially during pregnancy

| [http://www.disease-ontology.org/?id=DOID:3240 DOID:3240]

|

|

|

|-

| aspirin-induced respiratory disease

| class of disease

| intrinsic asthma
salicylate sensitivity

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080822 DOID:0080822]

|

|

|

|-

| associative agnosia

| class of disease

| visual agnosia
agnosia

| agnosia that is a loss of the ability to recognize visual scenes or classes of objects but retain the abilty to describe them

| [http://www.disease-ontology.org/?id=DOID:0060136 DOID:0060136]

|

|

|

|-

| astereognosia

| class of disease

| agnosia
tactile agnosia

| agnosia that is the loss of the ability to recognize objects by touch based on its texture, size and weight

| [http://www.disease-ontology.org/?id=DOID:0060150 DOID:0060150]

|

|

|

|-

| asthma

| class of disease

| bronchospasm
disease

| long-term disease involving inflamed airways

| [http://www.disease-ontology.org/?id=DOID:2841 DOID:2841]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.127.108 C08.127.108]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.495.108 C08.381.495.108]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.674.095 C08.674.095]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.680.095 C20.543.480.680.095]

| Asthma

| File:Asthma.jpg

|-

| astigmatism

| class of disease
symptom or sign

| refractive error
disease
astigmatism

| refractive error characterized by the optics of the eye to focus a point object into a sharp focused image on the retina, has_symptom blurred vision.

| [http://www.disease-ontology.org/?id=DOID:11782 DOID:11782]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.744.212 C11.744.212]

| Astigmatism (eye)

| File:Astigmatism.jpg

|-

| astroblastoma

| class of disease

| astrocytoma

| glial tumor derived from the astroblast, a type of cell that closely resembles spongioblastoma and astrocytes

| [http://www.disease-ontology.org/?id=DOID:7305 DOID:7305]

|

| Astroblastoma

|

|-

| astrocytoma

| class of disease

| glioma
cerebrum cancer
central nervous system cancer
disease

| type of cancer of the brain originating in a particular kind of glial cells, star-shaped brain cells in the cerebrum called astrocytes

| [http://www.disease-ontology.org/?id=DOID:3069 DOID:3069]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.600.380.080 C04.557.465.625.600.380.080]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.670.380.080 C04.557.470.670.380.080]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.600.380.080 C04.557.580.625.600.380.080]

| Astrocytic tumors

| File:Astrocytoma.jpg

|-

| asymmetric motor neuropathy

| class of disease

| motor neuritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7559 DOID:7559]

|

|

|

|-

| asymptomatic dengue

| class of disease

| dengue fever
asymptomatic disease

| A dengue disease that results in infection, has material basis in Dengue virus [NCBITaxon:12637] with four serotypes (Dengue virus 1, 2, 3 and 4), which are transmitted by Aedes mosquito bite. The infection has no manifestations of symptoms.

| [http://www.disease-ontology.org/?id=DOID:0050143 DOID:0050143]

|

|

|

|-

| asymptomatic neurosyphilis

| class of disease

| tertiary neurosyphilis

| tertiary neurosyphilis that results in mild meningitis

| [http://www.disease-ontology.org/?id=DOID:10035 DOID:10035]

|

|

|

|-

| asynchronous multifocal osteogenic sarcoma

| class of disease

| multifocal osteogenic sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6697 DOID:6697]

|

|

|

|-

| ataxia and polyneuropathy, adult-onset

| class of disease

| genetic disease
mitochondrial disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111750 DOID:0111750]

|

|

|

|-

| ataxia with oculomotor apraxia type 3

| class of disease

| autosomal recessive cerebellar ataxia
oculomotor apraxia
spinocerebellar ataxia with axonal neuropathy type 2

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060557 DOID:0060557]

|

|

|

|-

| ataxic cerebral palsy

| class of disease

| cerebral palsy

| A cerebral palsy that is caused by damage to the cerebellum, which affects muscle coordination, particularly in the limb. Some individuals suffer from hypotonia, tremors, difficulty with visual and/or auditory processing.

| [http://www.disease-ontology.org/?id=DOID:0050670 DOID:0050670]

|

|

|

|-

| atheroembolism of kidney

| class of disease

| cholesterol embolism
kidney disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1460 DOID:1460]

|

|

|

|-

| atherosclerosis

| class of disease

| arteriosclerotic cardiovascular disease
arteriosclerosis
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1936 DOID:1936]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.137.126.307 C14.907.137.126.307]

| Atherosclerosis

| File:Endothelial dysfunction Atherosclerosis.png

|-

| atopic dermatitis

| class of disease
symptom or sign

| dermatitis
allergic contact dermatitis
disease

| type of inflammation of the skin

| [http://www.disease-ontology.org/?id=DOID:3310 DOID:3310]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.850.210 C16.320.850.210]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.174.193 C17.800.174.193]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.815.193 C17.800.815.193]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.827.210 C17.800.827.210]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.343 C20.543.480.343]

| Atopic dermatitis

| File:Atopic dermatitis.png

|-

| atopic dermatitis 2

| class of disease

| atopic dermatitis

| atopic dermatitis conferred by variation in the FLG gene on chromosome 1q21

| [http://www.disease-ontology.org/?id=DOID:0110098 DOID:0110098]

|

|

|

|-

| atopic dermatitis 3

| class of disease

| atopic dermatitis

| atopic dermatitis associated with variation in the region 20p

| [http://www.disease-ontology.org/?id=DOID:0110099 DOID:0110099]

|

|

|

|-

| atopic dermatitis 4

| class of disease

| atopic dermatitis

| An atopic dermatitis associated with variation in the region 17q25.3.

| [http://www.disease-ontology.org/?id=DOID:0110100 DOID:0110100]

|

|

|

|-

| atopic dermatitis 5

| class of disease

| atopic dermatitis

| atopic dermatitis associated with variation in the region 13q12-q14

| [http://www.disease-ontology.org/?id=DOID:0110101 DOID:0110101]

|

|

|

|-

| atopic dermatitis 6

| class of disease

| atopic dermatitis

| atopic dermatitis associated with variation in the region 5q31-q33

| [http://www.disease-ontology.org/?id=DOID:0110102 DOID:0110102]

|

|

|

|-

| atopic dermatitis 7

| class of disease

| atopic dermatitis

| An atopic dermatitis associated with variation in the region 11q13.5.

| [http://www.disease-ontology.org/?id=DOID:0110103 DOID:0110103]

|

|

|

|-

| atopic dermatitis 8

| class of disease

| atopic dermatitis

| An atopic dermatitis associated with variation in the region 4q22.1.

| [http://www.disease-ontology.org/?id=DOID:0110104 DOID:0110104]

|

|

|

|-

| atopic dermatitis 9

| class of disease

| atopic dermatitis

| atopic dermatitis associated with variation in the region 3p24

| [http://www.disease-ontology.org/?id=DOID:0110105 DOID:0110105]

|

|

|

|-

| atrial heart septal defect 1

| class of disease

| atrial heart septal defect

| atrial heart septal defect type 1 associated with variation in the region 5p

| [http://www.disease-ontology.org/?id=DOID:0110106 DOID:0110106]

|

|

|

|-

| atrophic gastritis

| class of disease

| gastritis
chronic gastritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8929 DOID:8929]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.697.394 C06.405.205.697.394]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.398.394 C06.405.748.398.394]

| Atrophic gastritis

|

|-

| atrophic muscular disease

| class of disease

| neuromuscular disease
muscle tissue disease
muscular disease

| neuromuscular disease characterized by an abnormal reduction in the muscle volume and atrophy

| [http://www.disease-ontology.org/?id=DOID:913 DOID:913]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.534 C05.651.534]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.491.175 C10.668.491.175]

|

|

|-

| atrophic nonflaccid tympanic membrane

| class of disease

| tympanic membrane disease
Tympanic membrane retraction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12546 DOID:12546]

|

|

|

|-

| atrophic vaginitis

| class of disease

| vaginitis
disease

| inflammation of the vagina due to the thinning and shrinking of the tissues, as well as decreased lubrication

| [http://www.disease-ontology.org/?id=DOID:11968 DOID:11968]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.894.906.316 C13.351.500.894.906.316]

| Atrophic vaginitis

|

|-

| atrophic vulva

| class of disease

| vulvar disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14275 DOID:14275]

|

|

|

|-

| atrophodermia vermiculata

| class of disease

| keratosis pilaris atropicans

| Dermatological condition

| [http://www.disease-ontology.org/?id=DOID:0080756 DOID:0080756]

|

|

|

|-

| atrophy of prostate

| class of disease

| prostate disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2301 DOID:2301]

|

|

|

|-

| atypical Gaucher's disease due to saposin c deficiency

| class of disease

| Gaucher's disease
genetic disease

| A Gaucher's disease that has material basis in an autosomal recessive mutation of PSAP on chromosome 10q22.1.

| [http://www.disease-ontology.org/?id=DOID:0110961 DOID:0110961]

|

|

|

|-

| atypical autism

| class of disease

| autism spectrum disorder
pervasive developmental disorder
disease

| autism spectrum disorder that involves some autistic symptoms occuring after age 3 with an abscence of all the traits necessary for a diagnosis of autism

| [http://www.disease-ontology.org/?id=DOID:0060042 DOID:0060042]

|

|

|

|-

| atypical breast papilloma

| class of disease

| breast duct papilloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8227 DOID:8227]

|

|

|

|-

| atypical choroid plexus papilloma

| class of disease

| choroid plexus neoplasm
papilloma
cerebrovascular benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3544 DOID:3544]

|

|

|

|-

| atypical chronic myeloid leukemia

| class of disease

| myelodysplastic/myeloproliferative neoplasm
chronic myeloid leukemia

| A myelodysplastic myeloproliferative neoplasm characterized by the principal involvement of the neutrophil series with leukocytosis and multilineage dysplasia. The neoplastic cells do not have a Philadelphia chromosome or the BCR/ABL fusion gene.

| [http://www.disease-ontology.org/?id=DOID:0060597 DOID:0060597]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.539.300 C04.557.337.539.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.190.615.500 C15.378.190.615.500]

|

|

|-

| atypical depressive disorder

| class of disease

| mood disorder
disease

| depression characterized by improved mood in response to positive events

| [http://www.disease-ontology.org/?id=DOID:12294 DOID:12294]

|

| Atypical depression

|

|-

| atypical follicular adenoma

| class of disease

| follicular adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8292 DOID:8292]

|

|

|

|-

| atypical hereditary sensory neuropathy

| class of disease

| hereditary sensory and autonomic neuropathy

| hereditary sensory neuropathy characterized by late onset of sensory ataxia without ulcerating acropathy or autonomic abnormalities

| [http://www.disease-ontology.org/?id=DOID:0070160 DOID:0070160]

|

|

|

|-

| atypical lipomatous tumor

| class of disease

| liposarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5690 DOID:5690]

|

|

|

|-

| atypical neurofibroma

| class of disease

| neurofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5153 DOID:5153]

|

|

|

|-

| atypical polypoid adenomyoma

| class of disease

| adenomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4993 DOID:4993]

|

|

|

|-

| auditory agnosia

| class of disease

| agnosia
music-specific disorders

| agnosia that is a loss of the ability to distinguishing environmental and non-verbal auditory cues including difficulty distinguishing speech from non-speech sounds even though hearing is usually normal

| [http://www.disease-ontology.org/?id=DOID:0060137 DOID:0060137]

|

|

|

|-

| auricular cancer

| class of disease

| ear neoplasms

| human disease

| [http://www.disease-ontology.org/?id=DOID:5101 DOID:5101]

|

|

|

|-

| autoimmune atherosclerosis

| class of disease

| autoimmune disease of cardiovascular system

| autoimmune disease of cardiovascular system that is characterized by a build up of plaque in the arteries

| [http://www.disease-ontology.org/?id=DOID:0040096 DOID:0040096]

|

|

|

|-

| autoimmune cardiomyopathy

| class of disease

| autoimmune disease of cardiovascular system
heart disease
immune disorder
cardiomyopathy

| autoimmune disease of cardiovascular system that is characterized by deterioration of the function of the heart muscle

| [http://www.disease-ontology.org/?id=DOID:0040095 DOID:0040095]

|

|

|

|-

| autoimmune cholangitis

| class of disease

| autoimmune hepatitis
ascending cholangitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080742 DOID:0080742]

|

|

|

|-

| autoimmune disease

| class of disease

| hypersensitivity
disease
immune disorder
primary immunodeficiency disease

| type of human disease

| [http://www.disease-ontology.org/?id=DOID:417 DOID:417]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111 C20.111]

| Autoimmune diseases and disorders

| File:Warm autoimmune hemolytic anemia.jpg

|-

| autoimmune disease of blood

| class of disease

| autoimmune disease

| hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the blood

| [http://www.disease-ontology.org/?id=DOID:0060050 DOID:0060050]

|

|

|

|-

| autoimmune disease of cardiovascular system

| class of disease

| autoimmune disease
cardiovascular disease

| hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the cardiovascular system.

| [http://www.disease-ontology.org/?id=DOID:0060051 DOID:0060051]

|

|

|

|-

| autoimmune disease of central nervous system

| class of disease

| autoimmune disease of the nervous system
central nervous system disease

| autoimmune disease of the central nervous system

| [http://www.disease-ontology.org/?id=DOID:0060004 DOID:0060004]

|

|

|

|-

| autoimmune disease of endocrine system

| class of disease

| autoimmune disease
endocrine system disease

| hypersensitivity reaction type II disease that is the abnormal functioning of the immune system resulting in production of antibodies or T cells against cells and/or tissues in the endocrine system

| [http://www.disease-ontology.org/?id=DOID:0060005 DOID:0060005]

|

|

|

|-

| autoimmune disease of exocrine system

| class of disease

| autoimmune disease

| immune system disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the exocrine system

| [http://www.disease-ontology.org/?id=DOID:0060029 DOID:0060029]

|

|

|

|-

| autoimmune disease of eyes, ear, nose and throat

| class of disease

| autoimmune disease of the nervous system
sensory system disease

| hypersensitivity reaction type II disease of the eyes, ears, nose and throat

| [http://www.disease-ontology.org/?id=DOID:0060030 DOID:0060030]

|

|

|

|-

| autoimmune disease of gastrointestinal tract

| class of disease

| autoimmune disease
gastrointestinal system disease

| hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the gastrointestinal tract

| [http://www.disease-ontology.org/?id=DOID:0060031 DOID:0060031]

|

|

|

|-

| autoimmune disease of musculoskeletal system

| class of disease

| autoimmune disease
musculoskeletal disorder

| autoimmune disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the musculoskeletal system

| [http://www.disease-ontology.org/?id=DOID:0060032 DOID:0060032]

|

|

|

|-

| autoimmune disease of peripheral nervous system

| class of disease

| autoimmune disease of the nervous system
peripheral neuropathy

| autoimmune disease of the nervous system that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the peripheral nervous system

| [http://www.disease-ontology.org/?id=DOID:0060033 DOID:0060033]

|

|

|

|-

| autoimmune disease of the nervous system

| class of disease

| autoimmune disease
nervous system disease
neurological disorder

| A disorder characterized by the degeneration of the nervous system due to autoimmunity. Representative examples include multiple sclerosis, Guillain-Barre syndrome, and myasthenia gravis.

| [http://www.disease-ontology.org/?id=DOID:438 DOID:438]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.114 C10.114]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.258 C20.111.258]

|

|

|-

| autoimmune disease of urogenital tract

| class of disease

| autoimmune disease
reproductive system disease
urinary system disease

| hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the urogenital tract

| [http://www.disease-ontology.org/?id=DOID:0060049 DOID:0060049]

|

|

|

|-

| autoimmune gastritis

| class of disease

| autoimmune disease of gastrointestinal tract
stomach disease
gastritis

| autoimmune disease of gastrointestinal tract that is located in the stomach

| [http://www.disease-ontology.org/?id=DOID:0040090 DOID:0040090]

|

|

|

|-

| autoimmune glomerulonephritis

| class of disease

| autoimmune disease of urogenital tract
immune disorder
rare urogenital disease
glomerulonephritis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0040094 DOID:0040094]

|

|

|

|-

| autoimmune myocarditis

| class of disease

| autoimmune cardiomyopathy
myocarditis
autoimmune disease of cardiovascular system

|

| [http://www.disease-ontology.org/?id=DOID:0080767 DOID:0080767]

|

|

|

|-

| autoimmune neuropathy

| class of disease

| autoimmune disease of central nervous system

| autoimmune disease of centreal nervous system caused by an autoimmune response

| [http://www.disease-ontology.org/?id=DOID:0060499 DOID:0060499]

|

|

|

|-

| autoimmune optic neuritis

| class of disease

| autoimmune disease of peripheral nervous system
optic neuritis

| autoimmune disease of peripheral nervous system that is located in the neuron projection bundle connecting eye with brain

| [http://www.disease-ontology.org/?id=DOID:0040089 DOID:0040089]

|

|

|

|-

| autoimmune pancreatitis

| class of disease

| chronic pancreatitis
IgG4-related disease
autoimmune disease of endocrine system
pancreas disease

| type of chronic pancreatitis

| [http://www.disease-ontology.org/?id=DOID:0040091 DOID:0040091]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.689.750.830.500 C06.689.750.830.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.296 C20.111.296]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.291.500.750.500 C23.550.291.500.750.500]

|

|

|-

| autoimmune peripheral neuropathy

| class of disease

| autoimmune disease of peripheral nervous system

| autoimmune disease of peripheral nervous system that results in peripheral neuropathy

| [http://www.disease-ontology.org/?id=DOID:0040087 DOID:0040087]

|

|

|

|-

| autoimmune polyendocrine syndrome

| class of disease

| autoimmune disease of endocrine system
polyglandular dysfunction
disease

| autoimmune disease of endocrine system with auto-reactivity against endocrine organs

| [http://www.disease-ontology.org/?id=DOID:14040 DOID:14040]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.787 C19.787]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.750 C20.111.750]

|

|

|-

| autoimmune polyendocrine syndrome type 2

| class of disease

| autoimmune polyendocrine syndrome

| An autoimmune polyendocrine syndrome that is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs. It is more heterogeneous and has not been linked to one gene.

| [http://www.disease-ontology.org/?id=DOID:0050168 DOID:0050168]

|

|

|

|-

| autoimmune skin disease

| class of disease

| autoimmune disease
skin disease
rheumatic disease
cellulitis
rare skin disease
immune disorder
autoimmune disease of musculoskeletal system
connective tissue disease

| hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the skin and connective tissue

| [http://www.disease-ontology.org/?id=DOID:0060039 DOID:0060039]

|

|

|

|-

| autoimmune thyroiditis

| class of disease

| autoimmune disease of endocrine system
thyroiditis
disease

| autoimmune disease of endocrine system that involves inflammation located in thyroid gland caused by the immune system reacting against its own tissues

| [http://www.disease-ontology.org/?id=DOID:7188 DOID:7188]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.874.871.102 C19.874.871.102]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.809 C20.111.809]

|

|

|-

| autoimmune vasculitis

| class of disease

| autoimmune disease of cardiovascular system
immune disorder
vasculitis

| autoimmune disease of cardiovascular system that is characterized by inflammation of the blood vessels

| [http://www.disease-ontology.org/?id=DOID:0040097 DOID:0040097]

|

|

|

|-

| autonomic nervous system benign neoplasm

| class of disease

| peripheral nervous system benign neoplasm
autonomic nervous system neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080321 DOID:0080321]

|

|

|

|-

| autonomic nervous system disease

| class of disease

| peripheral neuropathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:11465 DOID:11465]

|

| Diseases and disorders of autonomic nervous system

|

|-

| autonomic nervous system neoplasm

| class of disease

| peripheral nervous system neoplasm
autonomic nervous system disease

| peripheral nervous system neoplasm that is located in the autonomic nervous system

| [http://www.disease-ontology.org/?id=DOID:2621 DOID:2621]

|

|

|

|-

| autonomic neuropathy

| class of disease

| autonomic nervous system disease
polyneuropathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:11504 DOID:11504]

|

|

|

|-

| autonomic peripheral neuropathy

| class of disease

| peripheral neuropathy
autonomic neuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060054 DOID:0060054]

|

|

|

|-

| autosomal dominant Aarskog syndrome

| class of disease

| Aarskog syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111825 DOID:0111825]

|

|

|

|-

| autosomal dominant Emery-Dreifuss muscular dystrophy 2

| class of disease

| Emery-Dreifuss muscular dystrophy
autosomal dominant disease

| Emery-Dreifuss muscular dystrophy that has material basis in an autosomal dominant mutation of LMNA on chromosome 1q22

| [http://www.disease-ontology.org/?id=DOID:0070247 DOID:0070247]

|

|

|

|-

| autosomal dominant Emery-Dreifuss muscular dystrophy 4

| class of disease

| Emery-Dreifuss muscular dystrophy
autosomal dominant disease

| An Emery-Dreifuss muscular dystrophy that has material basis in an autosomal dominant mutation of SYNE1 on chromosome 6q25.2.

| [http://www.disease-ontology.org/?id=DOID:0070249 DOID:0070249]

|

|

|

|-

| autosomal dominant Emery-Dreifuss muscular dystrophy 5

| class of disease

| Emery-Dreifuss muscular dystrophy
autosomal dominant disease

| An Emery-Dreifuss muscular dystrophy that has material basis in an autosomal dominant mutation of SYNE2 on chromosome 14q23.2.

| [http://www.disease-ontology.org/?id=DOID:0070250 DOID:0070250]

|

|

|

|-

| autosomal dominant Emery-Dreifuss muscular dystrophy 7

| class of disease

| Emery-Dreifuss muscular dystrophy
autosomal dominant disease

| An Emery-Dreifuss muscular dystrophy that has material basis in an autosomal dominant mutation of TMEM43 on chromosome 3p25.1.

| [http://www.disease-ontology.org/?id=DOID:0070252 DOID:0070252]

|

|

|

|-

| autosomal dominant Kenny-Caffey syndrome

| class of disease

| Kenny-Caffey syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080723 DOID:0080723]

|

|

|

|-

| autosomal dominant Parkinson disease 1

| class of disease

| hereditary late onset Parkinson disease
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060367 DOID:0060367]

|

|

|

|-

| autosomal dominant Parkinson's disease 22

| class of disease

| autosomal dominant disease
hereditary late onset Parkinson disease

| A late onset Parkinson's disease that has material basis in heterozygous mutation in the CHCHD2 gene on chromosome 7p11.2

| [http://www.disease-ontology.org/?id=DOID:0080504 DOID:0080504]

|

|

|

|-

| autosomal dominant Wolfram syndrome

| class of disease

| Wolfram syndrome
autosomal dominant disease

| Wolfram syndrome that is characterized by congenital progressive hearing impairment, diabetes mellitus, and optic atrophy and that has material basis in autosomal dominant inheritance of a heterozygous mutation in the WFS1 gene on chromosome 4p16

| [http://www.disease-ontology.org/?id=DOID:0080584 DOID:0080584]

|

|

|

|-

| autosomal dominant centronuclear myopathy

| class of disease

| centronuclear myopathy

| centronuclear myopathy that has material basis in autosomal dominant inheritance

| [http://www.disease-ontology.org/?id=DOID:0111217 DOID:0111217]

|

|

|

|-

| autosomal dominant chondrodysplasia punctata

| class of disease

| chondrodysplasia punctata
autosomal dominant disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060293 DOID:0060293]

|

|

|

|-

| autosomal dominant craniodiaphyseal dysplasia

| class of disease

| autosomal dominant disease
craniodiaphyseal dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080807 DOID:0080807]

|

|

|

|-

| autosomal dominant craniometaphyseal dysplasia

| class of disease

| autosomal dominant disease
craniometaphyseal dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080801 DOID:0080801]

|

|

|

|-

| autosomal dominant cutis laxa

| class of disease

| cutis laxa
autosomal dominant disease

| cutis laxa characterized by autosomal dominant inheritance of skin that is loose, hanging, wrinkled and lacking in elasticity

| [http://www.disease-ontology.org/?id=DOID:0070142 DOID:0070142]

|

|

|

|-

| autosomal dominant cutis laxa 1

| class of disease

| autosomal dominant cutis laxa

| autosomal dominant cutis laxa that has material basis in heterozygous mutations in the ELN gene on chromosome 7q11

| [http://www.disease-ontology.org/?id=DOID:0070130 DOID:0070130]

|

|

|

|-

| autosomal dominant cutis laxa 2

| class of disease

| autosomal dominant cutis laxa

| autosomal dominant cutis laxa that has material basis in heterozygous mutation in the FBLN5 gene on chromosome 14q32

| [http://www.disease-ontology.org/?id=DOID:0070136 DOID:0070136]

|

|

|

|-

| autosomal dominant disease

| class of disease

| autosomal genetic disease

| genetic disease characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease

| [http://www.disease-ontology.org/?id=DOID:0050736 DOID:0050736]

|

|

|

|-

| autosomal dominant distal hereditary motor neuropathy

| class of disease

| Distal hereditary motor neuropathies
spinal muscular atrophy
autosomal dominant disease

| Autosomal dominant form of distal hereditary motor neuropathy

| [http://www.disease-ontology.org/?id=DOID:0111198 DOID:0111198]

|

|

|

|-

| autosomal dominant dyskeratosis congenita 1

| class of disease

| dyskeratosis congenita
autosomal dominant disease

| A dyskeratosis congenita that has material basis in an autosomal dominant mutation of TERC on chromosome 3q26.2.

| [http://www.disease-ontology.org/?id=DOID:0070014 DOID:0070014]

|

|

|

|-

| autosomal dominant dyskeratosis congenita 2

| class of disease

| dyskeratosis congenita
autosomal dominant disease

| A dyskeratosis congenita that has material basis in an autosomal dominant mutation of TERT on chromosome 5p15.33.

| [http://www.disease-ontology.org/?id=DOID:0070016 DOID:0070016]

|

|

|

|-

| autosomal dominant dyskeratosis congenita 3

| class of disease

| dyskeratosis congenita
autosomal dominant disease

| dyskeratosis congenita that has material basis in an autosomal dominant mutation of TINF2 on chromosome 14q12

| [http://www.disease-ontology.org/?id=DOID:0070018 DOID:0070018]

|

|

|

|-

| autosomal dominant dyskeratosis congenita 4

| class of disease

| dyskeratosis congenita
autosomal dominant disease

| A dyskeratosis congenita that has material basis in an autosomal dominant mutation of RTEL1 on chromosome 20q13.33.

| [http://www.disease-ontology.org/?id=DOID:0070020 DOID:0070020]

|

|

|

|-

| autosomal dominant dyskeratosis congenita 6

| class of disease

| dyskeratosis congenita
autosomal dominant disease

| A dyskeratosis congenita that has material basis in an autosomal dominant mutation of ACD on chromosome 16q22.1.

| [http://www.disease-ontology.org/?id=DOID:0070023 DOID:0070023]

|

|

|

|-

| autosomal dominant hyaline body myopathy

| class of disease

| hyaline body myopathy
autosomal dominant disease

| A hyaline body myopathy that has material basis in heterozygous mutation in MYH7 on 14q11.2.

| [http://www.disease-ontology.org/?id=DOID:0111269 DOID:0111269]

|

|

|

|-

| autosomal dominant hypocalcemia

| class of disease

| hypocalcaemia
autosomal dominant disease
metal metabolism disorder

| calcium metabolism disease characterized by autosomal dominant inheritance of variable degrees of hypocalcemia with normal to low levels of parathyroid hormone

| [http://www.disease-ontology.org/?id=DOID:0090109 DOID:0090109]

|

|

|

|-

| autosomal dominant keratitis-ichthyosis-deafness syndrome

| class of disease

| autosomal dominant disease
keratitis–ichthyosis–deafness syndrome
syndrome

| autosomal dominant disease characterized by congenital deafness, keratopachydermia and constrictions of fingers and toes that has material basis in heterozygous mutation in the GJB2 gene on chromosome 13q

| [http://www.disease-ontology.org/?id=DOID:0060871 DOID:0060871]

|

|

|

|-

| autosomal dominant limb-girdle muscular dystrophy type 1

| class of disease

| autosomal dominant limb-girdle muscular dystrophy

| autosomal dominant limb-girdle muscular dystrophy that has material basis in heterozygous mutation in the DNAJB6 gene on chromosome 7q36

| [http://www.disease-ontology.org/?id=DOID:0110305 DOID:0110305]

|

|

|

|-

| autosomal dominant limb-girdle muscular dystrophy type 1H

| class of disease

| autosomal dominant limb-girdle muscular dystrophy

| An autosomal dominant limb-girdle muscular dystrophy that has material basis in with variation in the region 3p25.1-p23.

| [http://www.disease-ontology.org/?id=DOID:0110303 DOID:0110303]

|

|

|

|-

| autosomal dominant mental retardation 45

| class of disease

| autosomal dominant non-syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080236 DOID:0080236]

|

|

|

|-

| autosomal dominant mental retardation 46

| class of disease

| autosomal dominant non-syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080237 DOID:0080237]

|

|

|

|-

| autosomal dominant mental retardation 47

| class of disease

| autosomal dominant non-syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080238 DOID:0080238]

|

|

|

|-

| autosomal dominant mental retardation 48

| class of disease

| autosomal dominant non-syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080235 DOID:0080235]

|

|

|

|-

| autosomal dominant mental retardation 49

| class of disease

| autosomal dominant non-syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080234 DOID:0080234]

|

|

|

|-

| autosomal dominant mental retardation 50

| class of disease

| autosomal dominant non-syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080233 DOID:0080233]

|

|

|

|-

| autosomal dominant mental retardation 51

| class of disease

| autosomal dominant non-syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080232 DOID:0080232]

|

|

|

|-

| autosomal dominant mental retardation 52

| class of disease

| autosomal dominant non-syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080231 DOID:0080231]

|

|

|

|-

| autosomal dominant mental retardation 53

| class of disease

| autosomal dominant non-syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080228 DOID:0080228]

|

|

|

|-

| autosomal dominant mental retardation 54

| class of disease

| autosomal dominant non-syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080230 DOID:0080230]

|

|

|

|-

| autosomal dominant mental retardation 55

| class of disease

| autosomal dominant disease
syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080227 DOID:0080227]

|

|

|

|-

| autosomal dominant mental retardation 56

| class of disease

| autosomal dominant disease
syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080226 DOID:0080226]

|

|

|

|-

| autosomal dominant microcephaly

| class of disease

| autosomal dominant disease
microcephaly

| human disease

| [http://www.disease-ontology.org/?id=DOID:14725 DOID:14725]

|

|

|

|-

| autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques

| class of disease

| autosomal dominant disease
Olmsted syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112013 DOID:0112013]

|

|

|

|-

| autosomal dominant nocturnal frontal lobe epilepsy 1

| class of disease

| autosomal dominant nocturnal frontal lobe epilepsy

| autosomal dominant nocturnal frontal lobe epilepsy that has material basis in heterozygous mutation in the CHRNA4 gene on chromosome 20q13

| [http://www.disease-ontology.org/?id=DOID:0060682 DOID:0060682]

|

|

|

|-

| autosomal dominant nocturnal frontal lobe epilepsy 2

| class of disease

| autosomal dominant nocturnal frontal lobe epilepsy

| autosomal dominant nocturnal frontal lobe epilepsy that has material basis in variation in the chromosome region 15q24

| [http://www.disease-ontology.org/?id=DOID:0060683 DOID:0060683]

|

|

|

|-

| autosomal dominant nocturnal frontal lobe epilepsy 5

| class of disease

| autosomal dominant nocturnal frontal lobe epilepsy

| autosomal dominant nocturnal frontal lobe epilepsy that has material basis in heterozygous mutation in the KCNT1 gene on chromosome 9q34

| [http://www.disease-ontology.org/?id=DOID:0060686 DOID:0060686]

|

|

|

|-

| autosomal dominant non-syndromic intellectual disability 1

| class of disease

| autosomal dominant non-syndromic intellectual disability

| An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of MBD5 on chromosome 2q23.1.

| [http://www.disease-ontology.org/?id=DOID:0070031 DOID:0070031]

|

|

|

|-

| autosomal dominant non-syndromic intellectual disability 2

| class of disease

| autosomal dominant non-syndromic intellectual disability

| autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of DOCK8 on chromosome 9p24

| [http://www.disease-ontology.org/?id=DOID:0070032 DOID:0070032]

|

|

|

|-

| autosomal dominant nonsyndromic deafness 1

| class of disease

| autosomal dominant nonsyndromic deafness

| autosomal dominant nonsyndromic deafness that is characterized by low frequency progressive hearing loss and has material basis in mutation in the DIAPH1 gene on chromosome 5q31

| [http://www.disease-ontology.org/?id=DOID:0110541 DOID:0110541]

|

|

|

|-

| autosomal dominant nonsyndromic deafness 18

| class of disease

| autosomal dominant nonsyndromic deafness

| autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 3q22

| [http://www.disease-ontology.org/?id=DOID:0110549 DOID:0110549]

|

|

|

|-

| autosomal dominant nonsyndromic deafness 30

| class of disease

| autosomal dominant nonsyndromic deafness

| autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 15q25-q26

| [http://www.disease-ontology.org/?id=DOID:0110560 DOID:0110560]

|

|

|

|-

| autosomal dominant nonsyndromic deafness 33

| class of disease

| autosomal dominant nonsyndromic deafness

| autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 13q34

| [http://www.disease-ontology.org/?id=DOID:0110562 DOID:0110562]

|

|

|

|-

| autosomal dominant nonsyndromic deafness 47

| class of disease

| autosomal dominant nonsyndromic deafness

| autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 9p22-p21

| [http://www.disease-ontology.org/?id=DOID:0110570 DOID:0110570]

|

|

|

|-

| autosomal dominant nonsyndromic deafness 52

| class of disease

| autosomal dominant nonsyndromic deafness

| An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 5q31.1-q32.

| [http://www.disease-ontology.org/?id=DOID:0110578 DOID:0110578]

|

|

|

|-

| autosomal dominant nonsyndromic deafness 71

| class of disease

| autosomal dominant nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080267 DOID:0080267]

|

|

|

|-

| autosomal dominant nonsyndromic deafness 72

| class of disease

| autosomal dominant nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080268 DOID:0080268]

|

|

|

|-

| autosomal dominant nonsyndromic deafness 77

| class of disease

| autosomal dominant nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112168 DOID:0112168]

|

|

|

|-

| autosomal dominant nonsyndromic deafness 79

| class of disease

| autosomal dominant nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112160 DOID:0112160]

|

|

|

|-

| autosomal dominant optic atrophy and cataract

| class of disease

| autosomal dominant optic atrophy
optic atrophy
autosomal dominant disease

| gene (19q13.32).

| [http://www.disease-ontology.org/?id=DOID:0111433 DOID:0111433]

|

|

|

|-

| autosomal dominant optic atrophy plus syndrome

| class of disease

| autosomal dominant optic atrophy
syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111340 DOID:0111340]

|

|

|

|-

| autosomal dominant osteopetrosis 1

| class of disease

| osteopetrosis
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110937 DOID:0110937]

|

|

|

|-

| autosomal dominant progressive external ophthalmoplegia 1

| class of disease

| autosomal dominant disease
chronic progressive external ophthalmoplegia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111521 DOID:0111521]

|

|

|

|-

| autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6

| class of disease

| autosomal dominant disease
chronic progressive external ophthalmoplegia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111519 DOID:0111519]

|

|

|

|-

| autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2

| class of disease

| chronic progressive external ophthalmoplegia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111517 DOID:0111517]

|

|

|

|-

| autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3

| class of disease

| autosomal dominant disease
chronic progressive external ophthalmoplegia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111520 DOID:0111520]

|

|

|

|-

| autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4

| class of disease

| chronic progressive external ophthalmoplegia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111525 DOID:0111525]

|

|

|

|-

| autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5

| class of disease

| chronic progressive external ophthalmoplegia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111518 DOID:0111518]

|

|

|

|-

| autosomal dominant sensory ataxia 1

| class of disease

| hereditary ataxia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111170 DOID:0111170]

|

|

|

|-

| autosomal dominant severe congenital neutropenia

| class of disease

| severe congenital neutropenia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112130 DOID:0112130]

|

|

|

|-

| autosomal dominant spondyloepiphyseal dysplasia tarda

| class of disease

| autosomal dominant disease
spondyloepiphyseal dysplasia tarda

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112285 DOID:0112285]

|

|

|

|-

| autosomal dominant thrombophilia due to protein C deficiency

| class of disease

| protein C deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111909 DOID:0111909]

|

|

|

|-

| autosomal dominant woolly hair

| class of disease

| woolly hair
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111573 DOID:0111573]

|

|

|

|-

| autosomal genetic disease

| class of disease

| monogenic disease

| monogenic disease that is has material basis in a mutation in a single gene on one of the non-sex chromosomes

| [http://www.disease-ontology.org/?id=DOID:0050739 DOID:0050739]

|

| Autosomal diseases

|

|-

| autosomal hemophilia A

| class of disease

| blood coagulation disease
autosomal genetic disease
hemophilia A

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111823 DOID:0111823]

|

|

|

|-

| autosomal recessive Alport syndrome

| class of disease

| Alport syndrome
autosomal recessive disease

| Alport syndrome that has material -basis in homozygous or compound heterozygous mutation in the COL4A3 or the COL4A4 gene, both of which map to chromosome 2q

| [http://www.disease-ontology.org/?id=DOID:0110033 DOID:0110033]

|

|

|

|-

| autosomal recessive Kenny-Caffey syndrome

| class of disease

| Kenny-Caffey syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080722 DOID:0080722]

|

|

|

|-

| autosomal recessive Robinow syndrome

| class of disease

| Robinow syndrome
autosomal recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060764 DOID:0060764]

|

|

|

|-

| autosomal recessive centronuclear myopathy

| class of disease

| centronuclear myopathy
autosomal recessive disease

| inherited neuromuscular disorder defined by numerous centrally placed nuclei on muscle biopsy and clinical features of a congenital myopathy

| [http://www.disease-ontology.org/?id=DOID:0111216 DOID:0111216]

|

|

|

|-

| autosomal recessive chronic granulomatous disease cytochrome b-negative

| class of disease

| autosomal recessive disease
chronic granulomatous disease

| A chronic granulomatous disease characterized by autosomal recessive inheritance that has material basis in mutation in the CYBA gene on chromosome 16q24.2.

| [http://www.disease-ontology.org/?id=DOID:0070193 DOID:0070193]

|

|

|

|-

| autosomal recessive chronic granulomatous disease cytochrome b-positive type I

| class of disease

| chronic granulomatous disease
autosomal recessive disease

| A chronic granulomatous disease characterized by autosomal recessive inheritance that has material basis in mutation in the NCF1 gene on chromosome 7q11.23.

| [http://www.disease-ontology.org/?id=DOID:0070192 DOID:0070192]

|

|

|

|-

| autosomal recessive chronic granulomatous disease cytochrome b-positive type II

| class of disease

| autosomal recessive disease
chronic granulomatous disease

| chronic granulomatous disease characterized by autosomal recessive inheritance that has material basis in mutation in the NCF2 gene on chromosome 1q25

| [http://www.disease-ontology.org/?id=DOID:0070191 DOID:0070191]

|

|

|

|-

| autosomal recessive chronic granulomatous disease cytochrome b-positive type III

| class of disease

| autosomal recessive disease
chronic granulomatous disease

| chronic granulomatous disease characterized by that autosomal recessive inheritance has material basis in mutation in the NCF4 gene on chromosome 22q12

| [http://www.disease-ontology.org/?id=DOID:0070194 DOID:0070194]

|

|

|

|-

| autosomal recessive congenital bilateral absence of vas deferens

| class of disease

| autosomal recessive disease
congenital bilateral aplasia of the vas deferens

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111864 DOID:0111864]

|

|

|

|-

| autosomal recessive congenital ichthyosis

| class of disease

| autosomal recessive disease
congenital ichthyosis

| skin disease that is characterized by autosomal recessive inheritance and abnormal skin scaling over the whole body due to a defect in keratinization

| [http://www.disease-ontology.org/?id=DOID:0060655 DOID:0060655]

|

|

|

|-

| autosomal recessive congenital ichthyosis 1

| class of disease

| autosomal recessive congenital ichthyosis

| An autosomal recessive congenital ichthyosis characterized by lamellar ichthyosis, ectropion, eclabium and hyperkeratosis that has material basis in homozygous or compound heterozygous mutation in the TGM1 gene on chromosome 14q11.2.

| [http://www.disease-ontology.org/?id=DOID:0060656 DOID:0060656]

|

|

|

|-

| autosomal recessive congenital ichthyosis 13

| class of disease

| autosomal recessive congenital ichthyosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080257 DOID:0080257]

|

|

|

|-

| autosomal recessive congenital ichthyosis 14

| class of disease

| autosomal recessive congenital ichthyosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080258 DOID:0080258]

|

|

|

|-

| autosomal recessive congenital ichthyosis 7

| class of disease

| autosomal recessive congenital ichthyosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060716 DOID:0060716]

|

|

|

|-

| autosomal recessive craniometaphyseal dysplasia

| class of disease

| autosomal recessive disease
craniometaphyseal dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080802 DOID:0080802]

|

|

|

|-

| autosomal recessive cutis laxa type 2, classic type

| class of disease

| cutis laxa
autosomal recessive disease
autosomal recessive cutis laxa type 2

| cutis laxa characterized by generalized skin wrinkling, sparse subcutaneous fat, dysmorphic progeroid facial features and severe hypotonia

| [http://www.disease-ontology.org/?id=DOID:0070141 DOID:0070141]

|

|

|

|-

| autosomal recessive cutis laxa type I

| class of disease

| cutis laxa
autosomal recessive disease

| cutis laxa characterized by wrinkled, redundant and sagging inelastic skin and severe systemic manifestations particulary in the lungs, vasculature, and gastrointestinal and genitourinary systems

| [http://www.disease-ontology.org/?id=DOID:0070144 DOID:0070144]

|

|

|

|-

| autosomal recessive cutis laxa type IA

| class of disease

| autosomal recessive cutis laxa type I

| autosomal recessive cutis laxa type I that has material basis in homozygous or compound heterozygous mutation in the FBLN5 gene on chromosome 14q32

| [http://www.disease-ontology.org/?id=DOID:0070135 DOID:0070135]

|

|

|

|-

| autosomal recessive cutis laxa type IB

| class of disease

| autosomal recessive cutis laxa type I

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070133 DOID:0070133]

|

|

|

|-

| autosomal recessive cutis laxa type IC

| class of disease

| autosomal recessive cutis laxa type I

| autosomal recessive cutis laxa type I that has material basis in homozygous or compound heterozygous mutation in the LTBP4 gene on chromosome 19q13

| [http://www.disease-ontology.org/?id=DOID:0070139 DOID:0070139]

|

|

|

|-

| autosomal recessive cutis laxa type IIA

| class of disease

| autosomal recessive cutis laxa type 2, classic type

| autosomal recessive cutis laxa type II classic type that has material basis in homozygous or compound heterozygous mutations in the ATP6V0A2 gene on chromosome 12q24

| [http://www.disease-ontology.org/?id=DOID:0070134 DOID:0070134]

|

|

|

|-

| autosomal recessive cutis laxa type IIB

| class of disease

| cutis laxa
autosomal recessive disease
autosomal recessive cutis laxa type 2

| A cutis laxa characterized by progeroid features that has material basis in homozygous or compound heterozygous mutation in the PYCR1 gene on chromosome 17q25.3.

| [http://www.disease-ontology.org/?id=DOID:0070137 DOID:0070137]

|

|

|

|-

| autosomal recessive cutis laxa type IIIA

| class of disease

| De Barsy syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070132 DOID:0070132]

|

|

|

|-

| autosomal recessive cutis laxa type IIIB

| class of disease

| De Barsy syndrome

| autosomal recessive cutis laxa type III that has material basis in homozygous or compound heterozygous mutation in the PYCR1 gene on chromosome 17q25

| [http://www.disease-ontology.org/?id=DOID:0070138 DOID:0070138]

|

|

|

|-

| autosomal recessive disease

| class of disease

| autosomal genetic disease
disease

| genetic disease characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop

| [http://www.disease-ontology.org/?id=DOID:0050737 DOID:0050737]

|

| Autosomal recessive diseases

|

|-

| autosomal recessive distal hereditary motor neuronopathy

| class of disease

| autosomal recessive disease
spinal muscular atrophy

| spinal muscular atrophy that has material basis in autosomal recessive inheritance

| [http://www.disease-ontology.org/?id=DOID:0111197 DOID:0111197]

|

|

|

|-

| autosomal recessive dyskeratosis congenita 4

| class of disease

| dyskeratosis congenita
autosomal recessive disease

| A dyskeratosis congenita that has material basis in an autosomal recessive mutation of TERT on chromosome 5p15.33.

| [http://www.disease-ontology.org/?id=DOID:0070021 DOID:0070021]

|

|

|

|-

| autosomal recessive dyskeratosis congenita 5

| class of disease

| dyskeratosis congenita
autosomal recessive disease

| A dyskeratosis congenita that has material basis in an autosomal recessive mutation of RTEL1 on chromosome 20q13.33.

| [http://www.disease-ontology.org/?id=DOID:0070022 DOID:0070022]

|

|

|

|-

| autosomal recessive dyskeratosis congenita 6

| class of disease

| dyskeratosis congenita
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070024 DOID:0070024]

|

|

|

|-

| autosomal recessive early-onset Parkinson disease 23

| class of disease

| young-onset Parkinson disease
autosomal recessive disease

| early-onset Parkinson disease that has material basis in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22

| [http://www.disease-ontology.org/?id=DOID:0060896 DOID:0060896]

|

|

|

|-

| autosomal recessive hyaline body myopathy

| class of disease

| hyaline body myopathy
autosomal recessive disease

| A hyaline body myopathy that has material basis in compound heterozygous or homozygous mutation in MYH7 on 14q11.2.

| [http://www.disease-ontology.org/?id=DOID:0111268 DOID:0111268]

|

|

|

|-

| autosomal recessive intellectual developmental disorder-72

| class of disease

| syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080765 DOID:0080765]

|

|

|

|-

| autosomal recessive isolated ectopia lentis 2

| class of disease

| isolated ectopia lentis
autosomal recessive disease

| isolated ectopia lentis that has material basis in homozygous or compound heterozygous mutation in the ADAMTSL4 gene on chromosome 1q21

| [http://www.disease-ontology.org/?id=DOID:0111149 DOID:0111149]

|

|

|

|-

| autosomal recessive limb-girdle muscular dystrophy

| class of disease

| limb-girdle muscular dystrophy
autosomal recessive disease

| limb-girdle muscular dystrophy has material basis in autosomal recessive inheritance

| [http://www.disease-ontology.org/?id=DOID:0110274 DOID:0110274]

|

|

|

|-

| autosomal recessive limb-girdle muscular dystrophy type 2B

| class of disease

| autosomal recessive limb-girdle muscular dystrophy

| autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous or compound heterozygous mutation in the gene encoding the skeletal muscle protein dysferlin (DYSF) on chromosome 2p13

| [http://www.disease-ontology.org/?id=DOID:0110276 DOID:0110276]

|

|

|

|-

| autosomal recessive limb-girdle muscular dystrophy type 2C

| class of disease

| autosomal recessive limb-girdle muscular dystrophy
sarcoglycanopathy
qualitative or quantitative defects of gamma-sarcoglycan
neuromuscular disease with dilated cardiomyopathy

| autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous mutation in the gamma-sarcoglycan gene (SGCG) on chromosome 13q12

| [http://www.disease-ontology.org/?id=DOID:0110277 DOID:0110277]

|

|

|

|-

| autosomal recessive limb-girdle muscular dystrophy type 2Z

| class of disease

| disorder of O-xylosylglycan synthesis
autosomal recessive limb-girdle muscular dystrophy

| An autosomal recessive condition caused by mutation(s) in the POGLUT1 gene, encoding protein O-glucosyltransferase 1. It is characterized by progressive muscular dystrophy, primarily affecting the proximal muscles, resulting in difficulty walking.

| [http://www.disease-ontology.org/?id=DOID:0080762 DOID:0080762]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 100

| class of disease

| autosomal recessive nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111638 DOID:0111638]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 106

| class of disease

| autosomal recessive nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080261 DOID:0080261]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 107

| class of disease

| autosomal recessive nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080262 DOID:0080262]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 108

| class of disease

| autosomal recessive nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080263 DOID:0080263]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 109

| class of disease

| autosomal recessive nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111639 DOID:0111639]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 110

| class of disease

| autosomal recessive nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111644 DOID:0111644]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 111

| class of disease

| autosomal recessive nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111640 DOID:0111640]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 112

| class of disease

| autosomal recessive nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111637 DOID:0111637]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 113

| class of disease

| autosomal recessive nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111636 DOID:0111636]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 114

| class of disease

| autosomal recessive nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111642 DOID:0111642]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 115

| class of disease

| autosomal recessive nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111643 DOID:0111643]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 1A

| class of disease

| autosomal recessive nonsyndromic deafness

| autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has material basis in mutation in the GJB2 gene on chromosome 13q12

| [http://www.disease-ontology.org/?id=DOID:0110475 DOID:0110475]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 27

| class of disease

| autosomal recessive nonsyndromic deafness

| autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 2q23-q31

| [http://www.disease-ontology.org/?id=DOID:0110485 DOID:0110485]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 4

| class of disease

| autosomal recessive nonsyndromic deafness

| autosomal recessive nonsyndromic deafness that has material basis in mutation in the SLC26A4 gene on chromosome 7q22

| [http://www.disease-ontology.org/?id=DOID:0110498 DOID:0110498]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 40

| class of disease

| autosomal recessive nonsyndromic deafness

| An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 22q11.21-q12.1.

| [http://www.disease-ontology.org/?id=DOID:0110499 DOID:0110499]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 5

| class of disease

| autosomal recessive nonsyndromic deafness

| autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 14q12

| [http://www.disease-ontology.org/?id=DOID:0110507 DOID:0110507]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 57

| class of disease

| autosomal recessive nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111635 DOID:0111635]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 94

| class of disease

| autosomal recessive nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111641 DOID:0111641]

|

|

|

|-

| autosomal recessive nonsyndromic deafness 99

| class of disease

| autosomal recessive nonsyndromic deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111634 DOID:0111634]

|

|

|

|-

| autosomal recessive osteopetrosis 1

| class of disease

| osteopetrosis
autosomal recessive disease

| An osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the TCIRG1 gene on chromosome 11q13.2.

| [http://www.disease-ontology.org/?id=DOID:0110942 DOID:0110942]

|

|

|

|-

| autosomal recessive osteopetrosis 3

| class of disease

| osteopetrosis
autosomal recessive disease
renal tubular acidosis

| osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the CA2 gene on chromosome 8q21

| [http://www.disease-ontology.org/?id=DOID:0110941 DOID:0110941]

|

|

|

|-

| autosomal recessive pericentral pigmentary retinopathy

| class of disease

| retinitis pigmentosa
autosomal recessive disease

| retinitis pigmentosa that is characterized autosomal recessive inheritance of pigmentary retinal degeneration with onset in the infancy but slower rates of progression than other forms of retinopathy

| [http://www.disease-ontology.org/?id=DOID:0110422 DOID:0110422]

|

|

|

|-

| autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2

| class of disease

| autosomal recessive disease
chronic progressive external ophthalmoplegia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111515 DOID:0111515]

|

|

|

|-

| autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3

| class of disease

| chronic progressive external ophthalmoplegia
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111523 DOID:0111523]

|

|

|

|-

| autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4

| class of disease

| chronic progressive external ophthalmoplegia
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111516 DOID:0111516]

|

|

|

|-

| autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5

| class of disease

| autosomal recessive disease
chronic progressive external ophthalmoplegia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111524 DOID:0111524]

|

|

|

|-

| autosomal recessive pseudohypoaldosteronism type 1

| class of disease

| pseudohypoaldosteronism
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060854 DOID:0060854]

|

|

|

|-

| autosomal recessive pyridoxine-refractory sideroblastic anemia 3

| class of disease

| pyridoxine-refractory autosomal recessive sideroblastic anemia
autosomal recessive disease
sideroblastic anaemia P

| sideroblastic anemia that is characterized by homozygous or compound heterozygous mutation in the GLRX5 gene on chromosome 14q32

| [http://www.disease-ontology.org/?id=DOID:0080343 DOID:0080343]

|

|

|

|-

| autosomal recessive spinocerebellar ataxia 23

| class of disease

| autosomal recessive cerebellar ataxia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111613 DOID:0111613]

|

|

|

|-

| autosomal recessive spinocerebellar ataxia 24

| class of disease

| autosomal recessive cerebellar ataxia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111615 DOID:0111615]

|

|

|

|-

| autosomal recessive spinocerebellar ataxia 27

| class of disease

| autosomal recessive cerebellar ataxia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111616 DOID:0111616]

|

|

|

|-

| autosomal recessive spinocerebellar ataxia 3

| class of disease

| autosomal recessive cerebellar ataxia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111612 DOID:0111612]

|

|

|

|-

| autosomal recessive spinocerebellar ataxia 4

| class of disease

| autosomal recessive cerebellar ataxia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111611 DOID:0111611]

|

|

|

|-

| autosomal recessive spinocerebellar ataxia 6

| class of disease

| autosomal recessive cerebellar ataxia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111617 DOID:0111617]

|

|

|

|-

| autosomal recessive spinocerebellar ataxia 8

| class of disease

| autosomal recessive cerebellar ataxia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111618 DOID:0111618]

|

|

|

|-

| autosomal recessive spondyloepiphyseal dysplasia tarda

| class of disease

| spondyloepiphyseal dysplasia tarda
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112293 DOID:0112293]

|

|

|

|-

| autosomal recessive type IV Ehlers-Danlos syndrome

| class of disease

| Ehlers-Danlos syndrome
autosomal recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14759 DOID:14759]

|

|

|

|-

| autosomal-mitochondrial sensorineural deafness

| class of disease

| digenic disease
sensorineural hearing loss

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111752 DOID:0111752]

|

|

|

|-

| autotopagnosia

| class of disease

| agnosia

| form of agnosia

| [http://www.disease-ontology.org/?id=DOID:0060138 DOID:0060138]

|

|

|

|-

| avoidant personality disorder

| class of disease

| personality disorder
disease

| severe form of social anxiety

| [http://www.disease-ontology.org/?id=DOID:1509 DOID:1509]

|

| Avoidant personality disorder

|

|-

| axial osteomalacia

| class of disease

| osteosclerosis
osteomalacia
genetic disease

| osteosclerosis that results in coarsening located in trabecular bone

| [http://www.disease-ontology.org/?id=DOID:0080039 DOID:0080039]

|

|

|

|-

| axillary adentis

| class of disease

| lymphadenitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4640 DOID:4640]

|

|

|

|-

| axonal neuropathy

| class of disease

| peripheral neuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7319 DOID:7319]

|

|

|

|-

| azoospermia

| class of disease

| male infertility
oligospermia
disease

| male infertility disease characterized by the absence of any measurable level of sperm in semen

| [http://www.disease-ontology.org/?id=DOID:14227 DOID:14227]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.294.430.380 C12.200.294.430.380]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.100.500.430.380 C12.100.500.430.380]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.100.750.700.380 C12.100.750.700.380]

| Azoospermia

| File:Semen analysis.JPG

|-

| aztreonam allergy

| class of disease

| beta-lactam allergy

| beta-lactam allergy that has allergic trigger aztreonam

| [http://www.disease-ontology.org/?id=DOID:0040037 DOID:0040037]

|

|

|

|-

| bacillary angiomatosis

| class of disease

| bartonellosis
angiomatosis
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060345 DOID:0060345]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.400.126.100.075 C01.150.252.400.126.100.075]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.819.150 C01.150.252.819.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.800.720.150 C01.800.720.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.077.060 C14.907.077.060]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.838.765.150 C17.800.838.765.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.862.060 C17.800.862.060]

|

|

|-

| background diabetic retinopathy

| class of disease

| diabetic retinopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13208 DOID:13208]

|

|

|

|-

| bacterial esophagitis

| class of disease

| esophagitis
bacterial infectious disease

| An acute bacterial infection that affects the esophagus. Symptoms include severe pain on swallowing and retrosternal pain. Endoscopic examination reveals esophageal mucosal ulcerations and pseudomembranous formations.

| [http://www.disease-ontology.org/?id=DOID:13921 DOID:13921]

|

|

|

|-

| bacterial gastritis

| class of disease

| gastritis
bacterial infectious disease
chronic gastritis

| Gastritis resulting from bacteria

| [http://www.disease-ontology.org/?id=DOID:4033 DOID:4033]

|

|

|

|-

| bacterial sepsis

| class of disease

| bacterial infectious disease
sepsis

| bacterial infectious disease has material basis in Bacteria

| [http://www.disease-ontology.org/?id=DOID:0040085 DOID:0040085]

|

|

|

|-

| bacteriuria

| class of disease

| urinary system disease
disease

| medical term denoting the presence of bacteria in urine

| [http://www.disease-ontology.org/?id=DOID:1412 DOID:1412]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.915.219 C01.915.219]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.777.892.219 C12.200.777.892.219]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.968.892.219 C12.050.351.968.892.219]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.950.892.219 C12.950.892.219]

|

| File:Bacteriuria pyuria 4.jpg

|-

| bagassosis

| class of disease

| extrinsic allergic alveolitis

| silicosis

| [http://www.disease-ontology.org/?id=DOID:12522 DOID:12522]

|

|

|

|-

| balanitis

| class of disease
symptom or sign

| penile disease
inflammatory disease
disease

| infectious or non-infectious inflammation of the glans penis

| [http://www.disease-ontology.org/?id=DOID:13033 DOID:13033]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.494.136 C12.294.494.136]

| Balanitis

| File:Inflammation of the glans penis and the preputial mucosa.jpg

|-

| balanitis xerotica obliterans

| class of disease

| balanitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13477 DOID:13477]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.494.136.500 C12.294.494.136.500]

| Balanitis xerotica obliterans

| File:Balanitis xerotica obliterans.jpg

|-

| balanoposthitis

| class of disease

| penile disease
balanitis
posthitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:13031 DOID:13031]

|

| Balanoposthitis

|

|-

| baldness

| class of disease

| hair diseases
hairstyle
hair anomaly
absence
disease

| state where most or all of hair from the head has been lost or intentionally removed

| [http://www.disease-ontology.org/?id=DOID:987 DOID:987]

|

| Baldness

| File:PatrickStewart2004-08-03.jpg

|-

| balloon cell malignant melanoma

| class of disease

| skin melanoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10044 DOID:10044]

|

|

|

|-

| band keratopathy

| class of disease

| corneal degeneration

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11164 DOID:11164]

|

| Band keratopathy

|

|-

| barbiturate abuse

| class of disease

| substance abuse

| substance abuse that involves the recurring use of barbiturate drugs despite negative consequences

| [http://www.disease-ontology.org/?id=DOID:8519 DOID:8519]

|

|

|

|-

| barbiturate dependence

| class of disease

| barbiturate abuse
substance dependence

| drug dependence that involves the continued use of barbiturates despite problems related to use of the substance

| [http://www.disease-ontology.org/?id=DOID:2575 DOID:2575]

|

|

|

|-

| basal ganglia cerebrovascular disease

| class of disease

| basal ganglia disease
cerebrovascular disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10991 DOID:10991]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.079.127 C10.228.140.079.127]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.100 C10.228.140.300.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.061 C14.907.253.061]

|

|

|-

| basal ganglia disease

| class of disease

| encephalopathy

| brain disease that is characterized by dysfunction of the basal ganglia which help start and control movement

| [http://www.disease-ontology.org/?id=DOID:679 DOID:679]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.079 C10.228.140.079]

|

|

|-

| basal-cell carcinoma

| class of disease

| skin cancer
skin carcinoma
basal-cell neoplasm
disease

| subtype of basal-cell carcinoma most commonly occurring on the sun-exposed areas of the head and neck

| [http://www.disease-ontology.org/?id=DOID:2513 DOID:2513]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.165 C04.557.470.200.165]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.565.165 C04.557.470.565.165]

| Basal-cell carcinoma

| File:Basaliom1.jpg

|-

| basaloid large cell carcinoma of the lung

| class of disease

| large-cell lung carcinoma
squamous cell carcinoma of the lung
basaloid carcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:7045 DOID:7045]

|

|

|

|-

| basaloid squamous cell carcinoma

| class of disease

| squamous cell carcinoma
basaloid carcinoma
basal-cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5522 DOID:5522]

|

|

|

|-

| basaloid squamous cell skin carcinoma

| class of disease

| basaloid squamous cell carcinoma
keratinizing squamous cell carcinoma
skin cancer
squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7049 DOID:7049]

|

|

|

|-

| basidiobolomycosis

| class of disease

| subcutaneous mycosis
zygomycosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050278 DOID:0050278]

|

|

|

|-

| basilar artery insufficiency

| class of disease

| transient cerebral isolation
vertebrobasilar insufficiency
syndrome
artery disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:223 DOID:223]

|

|

|

|-

| basilar artery occlusion

| class of disease

| occlusion precerebral artery
artery disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13446 DOID:13446]

|

|

|

|-

| basosquamous carcinoma

| class of disease

| basal-cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5063 DOID:5063]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.170 C04.557.470.200.170]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.565.170 C04.557.470.565.170]

|

|

|-

| baylisascariasis

| class of disease

| parasitic helminthiasis infectious disease
spinal cord disease
eye disease
intestinal disease
encephalopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050259 DOID:0050259]

|

|

|

|-

| benign adult familial myoclonic epilepsy

| class of disease

| myoclonic epilepsy
adolescence-adult electroclinical syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111689 DOID:0111689]

|

|

|

|-

| benign blood vessel neoplasm

| class of disease

| vascular neoplasm
cardiovascular organ benign neoplasm

| benign neoplasm arising from arteries or veins

| [http://www.disease-ontology.org/?id=DOID:60006 DOID:60006]

|

| Benign vascular neoplasms

|

|-

| benign breast adenomyoepithelioma

| class of disease

| breast benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1641 DOID:1641]

|

|

|

|-

| benign breast phyllodes tumor

| class of disease

| breast benign neoplasm
phyllodes tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1631 DOID:1631]

|

|

|

|-

| benign deep fibrous histiocytoma

| class of disease

| immune system organ benign neoplasm
sclerosing hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4419 DOID:4419]

|

|

|

|-

| benign dermal neurilemmoma

| class of disease

| skin benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7181 DOID:7181]

|

|

|

|-

| benign eccrine breast spiradenoma

| class of disease

| breast benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1616 DOID:1616]

|

|

|

|-

| benign ependymoma

| class of disease

| benign glioma
ependymoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:4844 DOID:4844]

|

|

|

|-

| benign epilepsy with centrotemporal spikes

| class of disease

| childhood electroclinical syndrome
epilepsy syndrome

| the most common epilepsy syndrome in childhood which usually subsides with age

| [http://www.disease-ontology.org/?id=DOID:3329 DOID:3329]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490.360.280 C10.228.140.490.360.280]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490.493.250 C10.228.140.490.493.250]

|

|

|-

| benign essential hypertension

| class of disease

| essential hypertension

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10913 DOID:10913]

|

|

|

|-

| benign fibrous mesothelioma

| class of disease

| benign mesothelioma
solitary fibrous tumor of the pleura

| human disease

| [http://www.disease-ontology.org/?id=DOID:2653 DOID:2653]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.590.797.750 C04.557.450.565.590.797.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.894.797.640.800 C04.588.894.797.640.800]

|

|

|-

| benign hypertensive renal disease

| class of disease

| renal hypertension

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11520 DOID:11520]

|

|

|

|-

| benign intermediate mesothelioma

| class of disease

| benign mesothelioma

| human disease

| [http://www.disease-ontology.org/?id=DOID:5884 DOID:5884]

|

|

|

|-

| benign lymphoepithelial lesion of salivary gland

| class of disease

| salivary gland disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12899 DOID:12899]

|

|

|

|-

| benign mammary dysplasia

| class of disease

| breast benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9504 DOID:9504]

|

| Benign mammary dysplasias

|

|-

| benign mastocytoma

| class of disease

| benign neoplasms by histologic type

| human disease

| [http://www.disease-ontology.org/?id=DOID:4658 DOID:4658]

|

|

|

|-

| benign mediastinal neurilemmoma

| class of disease

| benign neurilemmoma
mediastinal neurilemmoma
benign neoplasm of mediastinum

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7922 DOID:7922]

|

|

|

|-

| benign mediastinal psammomatous neurilemmoma

| class of disease

| benign mediastinal neurilemmoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7921 DOID:7921]

|

|

|

|-

| benign meningioma

| class of disease

| meningioma
benign neoplasm of meninges
central nervous system organ benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4587 DOID:4587]

|

|

|

|-

| benign mesothelioma

| class of disease

| angiomyolipoma

| cell type benign neoplasm that has material basis in mesothelium

| [http://www.disease-ontology.org/?id=DOID:2645 DOID:2645]

|

|

|

|-

| benign neonatal seizures

| class of disease

| neonatal period electroclinical syndrome

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14264 DOID:14264]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490.370 C10.228.140.490.370]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.614.258 C16.614.258]

|

|

|-

| benign neoplasm

| class of disease

| disease of cellular proliferation
neoplasm
disease

| disease of cellular proliferation that results in abnormal growths in the body which lack the ability to metastasize

| [http://www.disease-ontology.org/?id=DOID:0060072 DOID:0060072]

|

| Benign neoplasms

|

|-

| benign neoplasm of exocrine pancreas

| class of disease

| pancreatic exocrine neoplasm
benign neoplasm of pancreas
endocrine organ benign neoplasm

| benign neoplasm that involves the exocrine pancreas

| [http://www.disease-ontology.org/?id=DOID:0080781 DOID:0080781]

|

|

|

|-

| benign neoplasm of lymph node

| class of disease

| lymph node neoplasm
immune system organ benign neoplasm

| benign neoplasm that involves the lymph node

| [http://www.disease-ontology.org/?id=DOID:0080617 DOID:0080617]

|

| Benign neoplasms of lymph nodes

|

|-

| benign neoplasms by histologic type

| class of disease

| benign neoplasm
neoplasms by histologic type

| benign neoplasm that is classified by the type of cell or tissue from which it is derived

| [http://www.disease-ontology.org/?id=DOID:0060084 DOID:0060084]

|

|

|

|-

| benign neurilemmoma

| class of disease

| neurilemmoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:955 DOID:955]

|

|

|

|-

| benign ovarian sex cord-stromal tumor

| class of disease

| ovarian sex cord-stromal tumor
sex cord-stromal benign neoplasm

| sex cord-stromal tumor arising from the ovary, without metastatic potential

| [http://www.disease-ontology.org/?id=DOID:0080370 DOID:0080370]

|

|

|

|-

| benign parathyroid gland neoplasm

| class of disease

| parathyroid neoplasm
endocrine organ benign neoplasm
parathyroid gland disease

| benign neoplasm that involves the parathyroid gland

| [http://www.disease-ontology.org/?id=DOID:60008 DOID:60008]

|

| Benign neoplasms of parathyroid gland

|

|-

| benign paroxysmal positional nystagmus

| class of disease

| peripheral vertigo
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:13941 DOID:13941]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.218.568.900.883.500 C09.218.568.900.883.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.951.500 C10.597.951.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.958.500 C23.888.592.958.500]

|

| File:Balance Disorder Illustration A.png

|-

| benign pericardial teratoma

| class of disease

| mature teratoma
benign neoplasm of pericardium
rare circulatory system disease
cardiovascular organ benign neoplasm
pericardium disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8012 DOID:8012]

|

|

|

|-

| benign peritoneal mesothelioma

| class of disease

| peritoneal benign neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:1789 DOID:1789]

|

|

|

|-

| benign perivascular tumor

| class of disease

| cardiovascular organ benign neoplasm
perivascular tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5238 DOID:5238]

|

|

|

|-

| benign pleural mesothelioma

| class of disease

| pleural cancer
respiratory system benign neoplasm
pleural disease
benign neoplasms by histologic type

| human disease

| [http://www.disease-ontology.org/?id=DOID:5157 DOID:5157]

|

|

|

|-

| benign prostate phyllodes tumor

| class of disease

| male reproductive organ benign neoplasm
prostate phyllodes tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2885 DOID:2885]

|

|

|

|-

| benign recurrent intrahepatic cholestasis 1

| class of disease

| benign recurrent intrahepatic cholestasis
autosomal recessive disease

| benign recurrent intrahepatic cholestasis characterized by typically autosomal recessive inheritance that has material basis in mutation in the ATP8B1 gene on chromosome 18q

| [http://www.disease-ontology.org/?id=DOID:0070231 DOID:0070231]

|

|

|

|-

| benign recurrent intrahepatic cholestasis 2

| class of disease

| benign recurrent intrahepatic cholestasis
autosomal recessive disease

| benign recurrent intrahepatic cholestasis characterized by autosomal recessive inheritance that has material basis in mutation in the ABCB11 gene on chromosome 2q31

| [http://www.disease-ontology.org/?id=DOID:0070232 DOID:0070232]

|

|

|

|-

| benign renovascular hypertension

| class of disease

| benign secondary hypertension
renal hypertension
renovascular hypertension

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13145 DOID:13145]

|

|

|

|-

| benign secondary hypertension

| class of disease

| secondary hypertension

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13143 DOID:13143]

|

|

|

|-

| benign shuddering attacks

| class of disease

| movement disorders
myoclonus

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1713 DOID:1713]

|

|

|

|-

| benign struma ovarii

| class of disease

| struma ovarii
ovarian benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5209 DOID:5209]

|

|

|

|-

| benign teratoma

| class of disease

| germ cell benign neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080602 DOID:0080602]

|

|

|

|-

| benign vaginal carcinosarcoma

| class of disease

| vaginal benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:135 DOID:135]

|

|

|

|-

| benzo[d]isothiazol-3-one allergic contact dermatitis

| class of disease

| allergic contact dermatitis

| allergic contact dermatitis that has allergic trigger benzo[d]isothiazol-3-one

| [http://www.disease-ontology.org/?id=DOID:0040075 DOID:0040075]

|

|

|

|-

| benzoic acid allergic contact dermatitis

| class of disease

| allergic contact dermatitis

| allergic contact dermatitis that has allergic trigger benzoic acid

| [http://www.disease-ontology.org/?id=DOID:0040057 DOID:0040057]

|

|

|

|-

| benzylpenicillin allergy

| class of disease

| beta-lactam allergy

| beta-lactam allergy that has allergic trigger benzylpenicillin

| [http://www.disease-ontology.org/?id=DOID:0040003 DOID:0040003]

|

|

|

|-

| beriberi

| class of disease

| nutritional deficiency disease
thiamine deficiency
disease

| nutritional thiamine deficiency disease in humans

| [http://www.disease-ontology.org/?id=DOID:13725 DOID:13725]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.654.521.500.133.699.827.223 C18.654.521.500.133.699.827.223]

| Beriberi

| File:Late stage of paralysis with atrophy in dry beriberi.jpg

|-

| berylliosis

| class of disease

| pneumoconiosis
occupational lung disease
Beryllium poisoning
respiratory allergy
disease

| pneumoconiosis that involves allergic response located in lungs caused by inhalation of beryllium compounds

| [http://www.disease-ontology.org/?id=DOID:10322 DOID:10322]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.483.581.225 C08.381.483.581.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.520.702.225 C08.381.520.702.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C24.800.225 C24.800.225]

| Berylliosis

| File:Chronic beryllioisis - Case 293 (15342093149).jpg

|-

| beta-lactam allergy

| class of disease

| drug allergy

| drug allergy triggered by a beta-lactam

| [http://www.disease-ontology.org/?id=DOID:0060519 DOID:0060519]

|

|

|

|-

| beta-thalassemia intermedia

| class of disease

| beta thalassemia

| Beta-thalassemia (BT) intermedia is a form of BT (see this term) characterized by mild to moderate anemia which does not or only occasionally requires transfusion

| [http://www.disease-ontology.org/?id=DOID:0080772 DOID:0080772]

|

|

|

|-

| beta-thalassemia major

| class of disease

| beta thalassemia

| Beta-thalassemia (BT) major is a severe early-onset form of BT (see this term) characterized by severe anemia requiring regular red blood cell transfusions

| [http://www.disease-ontology.org/?id=DOID:0080771 DOID:0080771]

|

|

|

|-

| bicipital tenosynovitis

| class of disease

| tenosynovitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14192 DOID:14192]

|

|

|

|-

| bilateral breast cancer

| class of disease

| breast carcinoma

| breast carcinoma that is characterized by an individual having breast cancer in both breasts, either simultaneously or at different times

| [http://www.disease-ontology.org/?id=DOID:6741 DOID:6741]

|

|

|

|-

| bilateral frontoparietal polymicrogyria

| class of disease

| autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080922 DOID:0080922]

|

|

|

|-

| bilateral hyperactive labyrinth

| class of disease

| labyrinthine dysfunction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14165 DOID:14165]

|

|

|

|-

| bilateral optic nerve hypoplasia

| class of disease

| autosomal dominant disease
optic nerve disease
optic nerve hypoplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111531 DOID:0111531]

|

|

|

|-

| bilateral renal aplasia

| class of disease

| renal agenesis

| renal agenesis that is characterized by the absence of both kidneys at birth

| [http://www.disease-ontology.org/?id=DOID:0080200 DOID:0080200]

|

|

|

|-

| bile duct adenocarcinoma

| class of disease

| bile duct carcinoma
adenocarcinoma of liver and intrahepatic biliary tract
adenocarcinoma

| bile duct carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:4896 DOID:4896]

|

|

|

|-

| bile duct adenoma

| class of disease

| liver neoplasm
biliary tract neoplasm
bile duct disease
gastrointestinal adenoma
benign neoplasms by histologic type
adenoma

| adenoma and biliary tract cancer that results in a small firm white nodule with multiple bile ducts that are located in a fibrous stroma

| [http://www.disease-ontology.org/?id=DOID:5381 DOID:5381]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.035.085 C04.557.470.035.085]

|

|

|-

| bile duct cancer

| class of disease

| biliary tract cancer
bile duct neoplasm
bile duct disease

| biliary tract cancer that is located in the bile duct

| [http://www.disease-ontology.org/?id=DOID:4606 DOID:4606]

|

|

|

|-

| bile duct carcinoma

| class of disease

| bile duct cancer
carcinoma

| bile duct cancer that has material basis in abnormally proliferating cells derives from epithelial cells

| [http://www.disease-ontology.org/?id=DOID:4897 DOID:4897]

|

|

|

|-

| bile duct carcinoma in situ

| class of disease

| in situ carcinoma
biliary tract neoplasm
bile duct disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050613 DOID:0050613]

|

|

|

|-

| bile duct clear cell adenocarcinoma

| class of disease

| bile duct adenocarcinoma
clear cell adenocarcinoma
extrahepatic bile duct adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7032 DOID:7032]

|

|

|

|-

| bile duct cystadenocarcinoma

| class of disease

| bile duct adenocarcinoma
bile duct cystadenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4075 DOID:4075]

|

|

|

|-

| bile duct cystadenoma

| class of disease

| bile duct adenoma
bile duct disease
biliary tract neoplasm
benign neoplasms by histologic type

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5384 DOID:5384]

|

|

|

|-

| bile duct disease

| class of disease

| biliary tract disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4138 DOID:4138]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.120 C06.130.120]

|

|

|-

| bile duct mucinous adenocarcinoma

| class of disease

| bile duct adenocarcinoma
extrahepatic bile duct adenocarcinoma
mucinous adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3698 DOID:3698]

|

|

|

|-

| bile duct mucoepidermoid carcinoma

| class of disease

| mucoepidermoid carcinoma
bile duct mucinous adenocarcinoma
bile duct cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4681 DOID:4681]

|

|

|

|-

| bile duct rhabdomyosarcoma

| class of disease

| bile duct sarcoma
rhabdomyosarcoma
bile duct cancer

| rhabdomyosarcoma and sarcoma of bile duct that is located in the bile duct

| [http://www.disease-ontology.org/?id=DOID:3254 DOID:3254]

|

|

|

|-

| bile duct sarcoma

| class of disease

| bile duct cancer
sarcoma

| sarcoma and malignant tumor of extrahepatic bile duct that is located in the bile duct

| [http://www.disease-ontology.org/?id=DOID:4064 DOID:4064]

|

|

|

|-

| bile duct signet ring cell carcinoma

| class of disease

| signet ring cell adenocarcinoma
bile duct carcinoma
extrahepatic bile duct adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3494 DOID:3494]

|

|

|

|-

| bile reflux

| class of disease

| biliary tract disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12237 DOID:12237]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.140 C06.130.140]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.240.140 C06.405.748.240.140]

|

|

|-

| biliary dyskinesia

| class of disease

| gallbladder disease
common bile duct disease

| gallbladder disease characterized by altered tonus of the sphincter of Oddi, disturbance in the coordination of contraction of the biliary ducts, and/or reduction in the speed of emptying of the biliary tree

| [http://www.disease-ontology.org/?id=DOID:4140 DOID:4140]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.120.250.098 C06.130.120.250.098]

|

|

|-

| biliary papillomatosis

| class of disease

| biliary tract neoplasm
papilloma

| biliary tract neoplasm characterized by multiple papillary tumors in the intrahepatic and/or extrahepatic biliary tree

| [http://www.disease-ontology.org/?id=DOID:5468 DOID:5468]

|

| Intraductal papillary neoplasm of the bile duct

| File:BileDuct IntraductalPapillaryNeoplasm MP CTR.jpg

|-

| biliary reflux

| class of disease

| duodenal disease
stomach disease
gastroesophageal reflux disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:4071 DOID:4071]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.275.700 C06.405.469.275.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.240 C06.405.748.240]

| Biliary reflux

|

|-

| biliary tract cancer

| class of disease

| hepatobiliary system cancer
biliary tract neoplasm

| gastrointestinal system cancer that results in malignant growth located in the gallbladder or located in the bile duct

| [http://www.disease-ontology.org/?id=DOID:4607 DOID:4607]

|

| Biliary tract cancers

|

|-

| biliary tract disease

| class of disease

| biliary disease
hepatobiliary disease

| disease involving the biliary tree

| [http://www.disease-ontology.org/?id=DOID:9741 DOID:9741]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130 C06.130]

|

|

|-

| biliary tract intraductal papillary mucinous neoplasm

| class of disease

| biliary tract neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:5469 DOID:5469]

|

|

|

|-

| biliary tract neoplasm

| class of disease

| hepatobiliary neoplasm
biliary tract disease

| hepatobiliary neoplasm located in the biliary tract

| [http://www.disease-ontology.org/?id=DOID:0050625 DOID:0050625]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.120 C04.588.274.120]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.320 C06.130.320]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.120 C06.301.120]

| Biliary tract neoplasms

|

|-

| bilirubin metabolic disorder

| class of disease

| inherited metabolic disorder
hyperbilirubinemia

| inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism

| [http://www.disease-ontology.org/?id=DOID:2741 DOID:2741]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.300 C16.320.565.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.300 C18.452.648.300]

|

|

|-

| binocular vision disease

| class of disease

| strabismus
vision disorder

| human disease

| [http://www.disease-ontology.org/?id=DOID:12667 DOID:12667]

|

|

|

|-

| biotin deficiency

| class of disease

| nutritional deficiency disease
vitamin deficiency
disease

| nutritional deficiency disease that is characterized by thinning of the hair (often with loss of hair color), and red scaly rash around the eyes, nose, and mouth

| [http://www.disease-ontology.org/?id=DOID:0050810 DOID:0050810]

|

|

|

|-

| biotinidase deficiency

| class of disease

| multiple carboxylase deficiency
disorder of other vitamins and cofactors metabolism and transport
rare genetic epilepsy
rare hereditary metabolic disease with peripheral neuropathy

| multiple carboxylase deficiency that involves a deficiency in biotinidase

| [http://www.disease-ontology.org/?id=DOID:856 DOID:856]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.100.620.100 C16.320.565.100.620.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.202.720.100 C16.320.565.202.720.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.100.620.100 C18.452.648.100.620.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.202.720.100 C18.452.648.202.720.100]

|

| File:Biotin structure.svg

|-

| biphasic synovial sarcoma

| class of disease

| synovial sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5492 DOID:5492]

|

|

|

|-

| bipolar I disorder

| class of disease

| bipolar disorder
disease

| bipolar disorder that is characterized by at least one manic or mixed episode

| [http://www.disease-ontology.org/?id=DOID:14042 DOID:14042]

|

|

|

|-

| bipolar II disorder

| class of disease

| bipolar disorder
disease

| bipolar disorder that is characterized by at least one hypomanic episode and at least one major depressive episode; with this disorder, depressive episodes are more frequent and more intense than manic episodes

| [http://www.disease-ontology.org/?id=DOID:0060166 DOID:0060166]

|

|

|

|-

| bipolar disorder

| class of disease

| mood disorder

| human mental illness characterized by mood changes

| [http://www.disease-ontology.org/?id=DOID:3312 DOID:3312]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.084.500 F03.084.500]

| Bipolar disorder

| File:Comedy and tragedy masks without background.svg

|-

| bird fancier's lung

| class of disease

| extrinsic allergic alveolitis
rare allergic respiratory disease

| extrinsic allergic alveolitis which is caused by inhalation of antigens from avian excreta, symptoms are abrupt onset of dyspnea, cough, malaise, and fever after exposure to antigen

| [http://www.disease-ontology.org/?id=DOID:13891 DOID:13891]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.483.125.125 C08.381.483.125.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.674.055.125 C08.674.055.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.680.075.125 C20.543.480.680.075.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C24.125 C24.125]

|

|

|-

| birdshot chorioretinopathy

| class of disease

| uveitis
white dot syndrome
posterior uveitis
non-infectious posterior uveitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111079 DOID:0111079]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.768.773.348.500 C11.768.773.348.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.160.478.400.500 C11.941.160.478.400.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.879.780.900.300.318.500 C11.941.879.780.900.300.318.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.879.780.900.650.250 C11.941.879.780.900.650.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.303 C20.111.303]

| Birdshot chorioretinopathy

|

|-

| bizarre leiomyoma

| class of disease

| leiomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5127 DOID:5127]

|

|

|

|-

| black piedra

| class of disease

| superficial mycosis
disease

| superficial mycosis that is a superficial fungal infection of the hair shaft caused by Piedraia hortae

| [http://www.disease-ontology.org/?id=DOID:12711 DOID:12711]

|

| Black piedra

|

|-

| bladder adenocarcinoma

| class of disease

| bladder carcinoma
adenocarcinoma

| bladder carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:3711 DOID:3711]

|

| Adenocarcinomas of the urinary bladder

|

|-

| bladder benign neoplasm

| class of disease

| urinary system benign neoplasm
bladder disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050623 DOID:0050623]

|

|

|

|-

| bladder calculus

| class of disease

| urolithiasis
bladder disease

| stone found in the urinary bladder

| [http://www.disease-ontology.org/?id=DOID:11355 DOID:11355]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.829.720 C12.777.829.720]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.967.500.925 C12.777.967.500.925]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.829.521 C13.351.968.829.521]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.967.500.925 C13.351.968.967.500.925]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.300.175.850.875 C23.300.175.850.875]

| Urinary bladder stones

| File:Bladder Stone 08783.jpg

|-

| bladder cancer

| class of disease

| urinary system cancer
bladder disease
bladder neoplasm
disease

| urinary system cancer that results in malignant growth located in the urinary bladder

| [http://www.disease-ontology.org/?id=DOID:11054 DOID:11054]

|

| Urinary bladder cancer

| File:Bladder urothelial carcinoma histopathology (2) at trigone.jpg

|-

| bladder carcinoma

| class of disease

| bladder cancer
carcinoma

| urinary bladder cancer that has material basis in abnormally proliferating cells derives from epithelial cells

| [http://www.disease-ontology.org/?id=DOID:4007 DOID:4007]

|

|

|

|-

| bladder carcinoma in situ

| class of disease

| non-invasive bladder urothelial carcinoma
bladder flat intraepithelial lesion
carcinoma in situ of breast and genitourinary system
bladder disease
in situ carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9053 DOID:9053]

|

|

|

|-

| bladder clear cell adenocarcinoma

| class of disease

| bladder adenocarcinoma
clear cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5306 DOID:5306]

|

|

|

|-

| bladder colloid adenocarcinoma

| class of disease

| bladder adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3710 DOID:3710]

|

|

|

|-

| bladder colonic type adenocarcinoma

| class of disease

| bladder adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6594 DOID:6594]

|

|

|

|-

| bladder diffuse clear cell adenocarcinoma

| class of disease

| bladder clear cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6210 DOID:6210]

|

|

|

|-

| bladder disease

| class of disease

| urinary system disease

| urinary system disease that is located in the bladder

| [http://www.disease-ontology.org/?id=DOID:365 DOID:365]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.829 C12.777.829]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.829 C13.351.968.829]

| Diseases and disorders of the urinary bladder

|

|-

| bladder diverticulum

| class of disease

| bladder disease
diverticulum
genetic disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11353 DOID:11353]

|

| Bladder diverticulum

|

|-

| bladder dome cancer

| class of disease

| bladder cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:11820 DOID:11820]

|

|

|

|-

| bladder exstrophy

| class of disease

| bladder disease
bladder exstrophy-epispadias-cloacal exstrophy complex
disease

| congenital disorder of urinary system

| [http://www.disease-ontology.org/?id=DOID:0080174 DOID:0080174]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.706.132 C12.706.132]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.829.132 C12.777.829.132]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.875.132 C13.351.875.132]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.829.132 C13.351.968.829.132]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.132 C16.131.939.132]

| Bladder exstrophy

| File:Classical bladder exstrophy.jpg

|-

| bladder exstrophy-epispadias-cloacal exstrophy complex

| class of disease

| congenital disorder
urinary system disease

| physical disorder that is characterized as a spectrum of anomalies involving the urinary tract, genital tract, musculoskeletal system and sometimes the intestinal tract

| [http://www.disease-ontology.org/?id=DOID:0080173 DOID:0080173]

|

|

|

|-

| bladder flat intraepithelial lesion

| class of disease

| bladder benign neoplasm
bladder cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5429 DOID:5429]

|

|

|

|-

| bladder hepatoid adenocarcinoma

| class of disease

| bladder adenocarcinoma
hepatoid adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8097 DOID:8097]

|

|

|

|-

| bladder lateral wall cancer

| class of disease

| bladder cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11593 DOID:11593]

|

|

|

|-

| bladder leiomyoma

| class of disease

| bladder benign neoplasm
leiomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13109 DOID:13109]

|

|

|

|-

| bladder lymphoma

| class of disease

| bladder cancer
primary organ-specific lymphoma
lymphoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:11821 DOID:11821]

|

|

|

|-

| bladder mixed adenocarcinoma

| class of disease

| bladder adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8096 DOID:8096]

|

|

|

|-

| bladder neck cancer

| class of disease

| bladder cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:11809 DOID:11809]

|

|

|

|-

| bladder neck obstruction

| class of disease

| urinary tract obstruction
bladder disease
bladder outlet obstruction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13948 DOID:13948]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.767.700.962 C12.777.767.700.962]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.829.760 C12.777.829.760]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.767.700.850 C13.351.968.767.700.850]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.829.601 C13.351.968.829.601]

|

|

|-

| bladder papillary clear cell adenocarcinoma

| class of disease

| bladder clear cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8051 DOID:8051]

|

|

|

|-

| bladder papillary transitional cell neoplasm

| class of disease

| urinary tract papillary transitional cell benign neoplasm
bladder cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5432 DOID:5432]

|

|

|

|-

| bladder sarcoma

| class of disease

| bladder cancer
sarcoma

| sarcoma and malignant neoplasm of urinary bladder that is located in the bladder

| [http://www.disease-ontology.org/?id=DOID:11812 DOID:11812]

|

|

|

|-

| bladder signet ring cell adenocarcinoma

| class of disease

| bladder adenocarcinoma
signet ring cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6481 DOID:6481]

|

|

|

|-

| bladder squamous cell carcinoma

| class of disease

| bladder carcinoma
squamous cell carcinoma

| carcinoma of bladder that is manifested in squamous cells of the bladder

| [http://www.disease-ontology.org/?id=DOID:3742 DOID:3742]

|

|

|

|-

| bladder squamous papilloma

| class of disease

| bladder benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13110 DOID:13110]

|

|

|

|-

| bladder transitional cell papilloma

| class of disease

| bladder papillary transitional cell neoplasm
transitional papilloma
urinary tract non-invasive transitional cell neoplasm
urinary system benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6933 DOID:6933]

|

|

|

|-

| bladder trigone cancer

| class of disease

| bladder cancer
bladder dome cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11813 DOID:11813]

|

|

|

|-

| bladder tubulo-cystic clear cell adenocarcinoma

| class of disease

| bladder clear cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8050 DOID:8050]

|

|

|

|-

| bladder urachal adenocarcinoma

| class of disease

| bladder urachal carcinoma
bladder adenocarcinoma
urachal cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7694 DOID:7694]

|

|

|

|-

| bladder urachal carcinoma

| class of disease

| bladder carcinoma
urachal cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5958 DOID:5958]

|

|

|

|-

| bladder urachal squamous cell carcinoma

| class of disease

| bladder urachal carcinoma
bladder squamous cell carcinoma
squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5957 DOID:5957]

|

|

|

|-

| bladder urachal urothelial carcinoma

| class of disease

| bladder urachal carcinoma
bladder urothelial carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7244 DOID:7244]

|

|

|

|-

| bladder urothelial carcinoma

| class of disease

| bladder carcinoma
transitional cell carcinoma

| bladder carcinoma that has material basis in transitional cells located in the lining of the bladder

| [http://www.disease-ontology.org/?id=DOID:4006 DOID:4006]

|

|

|

|-

| bladder urothelial papillary carcinoma

| class of disease

| bladder urothelial carcinoma
bladder papillary transitional cell neoplasm
papillary transitional carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6975 DOID:6975]

|

|

|

|-

| bladder verrucous squamous cell carcinoma

| class of disease

| bladder squamous cell carcinoma
verrucous carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3741 DOID:3741]

|

|

|

|-

| blastema predominant kidney Wilms' tumor

| class of disease

| nephroblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5182 DOID:5182]

|

|

|

|-

| blastoma

| class of disease

| cell type cancer
disease

| A cell type cancer that has material basis in abnormally proliferating cells derived from precursor cells called blast cells.

| [http://www.disease-ontology.org/?id=DOID:0070003 DOID:0070003]

|

| Blastomas

|

|-

| blepharitis

| class of disease
symptom or sign

| eyelid disease
eye inflammation
inflammatory disease
disease

| eyelid disease that is characterized by often chronic inflammation of the eyelid, generally the part where eyelashes grow

| [http://www.disease-ontology.org/?id=DOID:9423 DOID:9423]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.338.133 C11.338.133]

| Blepharitis

| File:Infant with blepharitis on the right side.jpg

|-

| blepharochalasis

| class of disease

| eyelid disease

| eyelid disease that is characterized by exacerbations and remissions of eyelid edema, which results in a stretching and subsequent atrophy of the eyelid tissue, leading to the formation of redundant folds over the lid margins

| [http://www.disease-ontology.org/?id=DOID:348 DOID:348]

|

|

|

|-

| blepharocheilodontic syndrome 1

| class of disease

| Blepharo-cheilo-odontic syndrome

| blepharocheilodontic syndrome that has material basis in heterozygous mutation in the CDH1 gene on chromosome 16q22

| [http://www.disease-ontology.org/?id=DOID:0080345 DOID:0080345]

|

|

|

|-

| blepharocheilodontic syndrome 2

| class of disease

| Blepharo-cheilo-odontic syndrome

| blepharocheilodontic syndrome that has material basis in heterozygous mutation in the CTNND1 gene on chromosome 11q12

| [http://www.disease-ontology.org/?id=DOID:0080346 DOID:0080346]

|

|

|

|-

| blepharoconjunctivitis

| class of disease

| blepharitis
conjunctivitis

| blepharitis that is characterized by the dual combination of conjunctivitis with blepharitis

| [http://www.disease-ontology.org/?id=DOID:2456 DOID:2456]

|

|

|

|-

| blepharophimosis

| class of disease

| eyelid disease
congenital physical abnormality
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10348 DOID:10348]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.250.090 C11.250.090]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.338.190 C11.338.190]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.384.190 C16.131.384.190]

| Blepharophimosis

| File:Blepharophimosis.png

|-

| blepharospasm

| class of disease

| focal dystonia
cranio-facial dystonia
disease

| focal dystonia that is characterized by the involuntary, forcible contraction of the muscles controlling eye blinks

| [http://www.disease-ontology.org/?id=DOID:529 DOID:529]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.338.250 C11.338.250]

|

| File:Gray379.png

|-

| blind hypertensive eye

| class of disease

| eye degenerative disease
glaucoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:11776 DOID:11776]

|

|

|

|-

| blind loop syndrome

| class of disease

| intestinal disease
small intestinal bacterial overgrowth

| intestinal disease characterized by a dysbalance of the bacterial flora of the small intestine, causing derangement to the normal physiological processes of digestion and absorption

| [http://www.disease-ontology.org/?id=DOID:10606 DOID:10606]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.637.145 C06.405.469.637.145]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.603.145 C18.452.603.145]

|

|

|-

| blindness

| class of disease
symptom or sign

| visual impairment
eye disease
vision symptom
sensory disability

| complete or nearly complete lack of vision; visual acuity worse than 3/60

| [http://www.disease-ontology.org/?id=DOID:1432 DOID:1432]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.751.941.162 C10.597.751.941.162]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.966.075 C11.966.075]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.763.941.162 C23.888.592.763.941.162]

| Visual impairment

| File:Watch for the blind.jpg

|-

| blood coagulation disease

| class of disease
symptom or sign

| hematopoietic system disease
hemic system symptom
disease

| condition in which the blood’s ability to coagulate (form clots) is impaired

| [http://www.disease-ontology.org/?id=DOID:1247 DOID:1247]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100 C15.378.100]

|

|

|-

| blood group incompatibility

| class of disease

| hematopoietic system disease
transfusion incident

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4176 DOID:4176]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=G09.188.114 G09.188.114]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=G12.186 G12.186]

|

|

|-

| blood platelet disease

| class of disease

| hematopoietic system disease
blood coagulation disease

| disorder of platelet function

| [http://www.disease-ontology.org/?id=DOID:2218 DOID:2218]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.140 C15.378.140]

|

|

|-

| blood protein disease

| class of disease

| hematopoietic system disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:620 DOID:620]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.147 C15.378.147]

|

|

|-

| blue toe syndrome

| class of disease

| foot diseases
cyanosis
cholesterol embolism

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14121 DOID:14121]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.355.350.454.500.200 C14.907.355.350.454.500.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.617.249 C14.907.617.249]

|

|

|-

| blunt duct adenosis of breast

| class of disease

| microglandular adenosis
non-proliferative fibrocystic change of the breast

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5996 DOID:5996]

|

|

|

|-

| body dysmorphic disorder

| class of disease

| somatoform disorder
hypochondriasis
disease

| mental disorder

| [http://www.disease-ontology.org/?id=DOID:0060163 DOID:0060163]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.875.149 F03.875.149]

| Body dysmorphic disorder

|

|-

| bone Ewing's sarcoma

| class of disease

| Ewing sarcoma

| peripheral primitive neuroectodermal tumor that is located in bone

| [http://www.disease-ontology.org/?id=DOID:3368 DOID:3368]

|

|

|

|-

| bone ameloblastoma

| class of disease

| bone benign neoplasm
ameloblastoma

| bone benign neoplasm that has material basis in odontogenic epithelium and is located in bone

| [http://www.disease-ontology.org/?id=DOID:0050895 DOID:0050895]

|

|

|

|-

| bone angioendothelial sarcoma

| class of disease

| osteosarcoma
vascular bone neoplasm
bone sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3351 DOID:3351]

|

|

|

|-

| bone benign neoplasm

| class of disease

| connective tissue benign neoplasm
bone disease
bone neoplasm
musculoskeletal system benign neoplasm

| connective tissue benign neoplasm that is located in bone

| [http://www.disease-ontology.org/?id=DOID:0060094 DOID:0060094]
[http://www.disease-ontology.org/?id=DOID:0060120 DOID:0060120]

|

|

|

|-

| bone cancer

| class of disease

| connective tissue neoplasm
bone disease
rare tumor
rare bone disease
musculoskeletal system cancer
bone neoplasm

| connective tissue cancer that is located in bone and is characterized by uncontrolled cellular proliferation that destroys normal bone tissue

| [http://www.disease-ontology.org/?id=DOID:184 DOID:184]

|

| Cancers of bone and articular cartilage

|

|-

| bone carcinoma

| class of disease

| bone cancer
carcinoma

| bone cancer that has material basis in abnormally proliferating cells derives from epithelial cells

| [http://www.disease-ontology.org/?id=DOID:2762 DOID:2762]

|

|

|

|-

| bone chondrosarcoma

| class of disease

| chondrosarcoma

| chondrosarcoma that is located in bone

| [http://www.disease-ontology.org/?id=DOID:0050897 DOID:0050897]

|

|

|

|-

| bone deterioration disease

| class of disease

| bone structure disease

| bone structure disease that results in change or damage of structure located in bone

| [http://www.disease-ontology.org/?id=DOID:0080007 DOID:0080007]

|

|

|

|-

| bone development disease

| class of disease

| bone disease

| bone disease that results in abnormal growth and development located in bone or located in cartilage

| [http://www.disease-ontology.org/?id=DOID:0080006 DOID:0080006]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.099 C05.116.099]

|

|

|-

| bone disease

| class of disease

| connective tissue disease

| medical condition which affects the bone

| [http://www.disease-ontology.org/?id=DOID:0080001 DOID:0080001]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116 C05.116]

| Osteopathies

|

|-

| bone epithelioid hemangioma

| class of disease

| bone benign neoplasm
histiocytoid hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6610 DOID:6610]

|

|

|

|-

| bone giant cell sarcoma

| class of disease

| malignant giant cell tumor
bone sarcoma

| malignant giant cell tumor that is composed of multinucleated giant cells

| [http://www.disease-ontology.org/?id=DOID:4719 DOID:4719]

|

|

|

|-

| bone inflammation disease

| class of disease

| bone disease
inflammation
disease

| inflammation of bone

| [http://www.disease-ontology.org/?id=DOID:3342 DOID:3342]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.680 C05.116.680]

|

|

|-

| bone leiomyosarcoma

| class of disease

| osteosarcoma
leiomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3367 DOID:3367]

|

|

|

|-

| bone lymphoma

| class of disease

| bone cancer
primary organ-specific lymphoma
lymphoma

| bone cancer and lymphoma by site that results in lymphoma starting in the bone

| [http://www.disease-ontology.org/?id=DOID:6759 DOID:6759]

|

|

|

|-

| bone marrow disease

| class of disease

| hematopoietic system disease
bone disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:4961 DOID:4961]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.190 C15.378.190]

|

|

|-

| bone osteosarcoma

| class of disease

| osteosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3376 DOID:3376]

|

|

|

|-

| bone peripheral neuroepithelioma

| class of disease

| bone Ewing's sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4388 DOID:4388]

|

|

|

|-

| bone remodeling disease

| class of disease

| bone disease

| bone disease that results in formation or resorption abnormalities located in bone

| [http://www.disease-ontology.org/?id=DOID:0080005 DOID:0080005]

|

|

|

|-

| bone resorption disease

| class of disease

| bone remodeling disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080011 DOID:0080011]

|

|

|

|-

| bone sarcoma

| class of disease

| sarcoma
bone cancer
bone neoplasm

| a sarcoma that arises from the bone, for example osteosarcoma and chondrosarcoma

| [http://www.disease-ontology.org/?id=DOID:0080639 DOID:0080639]

|

|

|

|-

| bone squamous cell carcinoma

| class of disease

| bone carcinoma
squamous cell carcinoma

| bone carcinoma that derives from squamous epithelial cells

| [http://www.disease-ontology.org/?id=DOID:0050896 DOID:0050896]

|

|

|

|-

| bone structure disease

| class of disease

| bone disease
spinal disease

| bone disease that has material basis in an abnormality in the location or function of the skeletal structure

| [http://www.disease-ontology.org/?id=DOID:0080010 DOID:0080010]

|

|

|

|-

| borderline glaucoma

| class of disease

| glaucoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9283 DOID:9283]

|

|

|

|-

| borderline personality disorder

| class of disease

| personality disorder
disease

| personality disorder characterized by variability of moods and unstable relationships

| [http://www.disease-ontology.org/?id=DOID:10930 DOID:10930]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.675.100 F03.675.100]

| Borderline personality disorder

| File:BPD 1.png

|-

| botryoid embryo rhabdomyosarcoma

| class of disease

| embryonal rhabdomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3255 DOID:3255]

|

|

|

|-

| bowel dysfunction

| class of disease

| intestinal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9779 DOID:9779]

|

|

|

|-

| bowel obstruction

| class of disease

| intestinal disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8437 DOID:8437]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.531 C06.405.469.531]

| Intestinal obstruction

| File:Upright abdominal X-ray demonstrating a bowel obstruction.jpg

|-

| brachial plexus lesion

| class of disease

| brachial plexus neuropathy
nerve injury
neck injury
disease

| brachial plexus neuropathy characterized by an abnormality, usually caused by disease or trauma, located in the brachial plexus

| [http://www.disease-ontology.org/?id=DOID:8443 DOID:8443]

|

| Brachial plexus injury

|

|-

| brachial plexus neoplasm

| class of disease

| nerve plexus neoplasm
brachial plexus neuropathy
central nervous system cancer

| neoplasm (disease) that involves the brachial nerve plexus

| [http://www.disease-ontology.org/?id=DOID:5913 DOID:5913]

|

|

|

|-

| brachial plexus neuritis

| class of disease

| neuritis
brachial plexus neuropathy

| An inflammatory process affecting the brachial plexus. It results in severe pain in the upper extremity and shoulder, upper arm weakness and loss of sensation in the upper arm.

| [http://www.disease-ontology.org/?id=DOID:3689 DOID:3689]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.100.500 C10.668.829.100.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.650.250 C10.668.829.650.250]

|

|

|-

| brachial plexus neuropathy

| class of disease

| plexopathy
peripheral neuropathy

| brachial plexus disorder characterized by regional paresthesia, pain and muscle weakness, and limited movement in the arm or hand

| [http://www.disease-ontology.org/?id=DOID:3690 DOID:3690]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.100 C10.668.829.100]

| Brachial plexus neuropathies

|

|-

| brachydactyly

| class of disease

| dysostosis
hand congenital deformity
disease

| bone development disease characterized by short fingers and toes

| [http://www.disease-ontology.org/?id=DOID:0050581 DOID:0050581]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.660.585.262 C05.660.585.262]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.621.585.262 C16.131.621.585.262]

| Brachydactyly

| File:Brachydaktylia.svg

|-

| brachydactyly type A1B

| class of disease

| brachydactyly type A1

| A brachydactyly type A1 characterized by shortened middle phalanges of all the digits and shortened proximal phalanges of the thumbs and big toes but normal stature that has material basis in variation in the chromosome region 5p13.3-p13.2.

| [http://www.disease-ontology.org/?id=DOID:0110974 DOID:0110974]

|

|

|

|-

| bradyopsia

| class of disease

| retinal disease
genetic vitreous-retinal disease

| retinal disease characterized by the slower than usual adaptation of the eyes to changing light conditions; can have material basis in mutations in the RGS9 or the R9AP genes

| [http://www.disease-ontology.org/?id=DOID:0050335 DOID:0050335]

|

|

|

|-

| brain angioma

| class of disease

| hemangioma
central nervous system organ benign neoplasm
encephalopathy
cerebrovascular disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5393 DOID:5393]

|

|

|

|-

| brain cancer

| class of disease

| central nervous system cancer
brain tumor
encephalopathy
cancer

| central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain

| [http://www.disease-ontology.org/?id=DOID:1319 DOID:1319]

|

|

|

|-

| brain compression

| class of disease

| encephalopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11457 DOID:11457]

|

|

|

|-

| brain ependymoma

| class of disease

| brain glioma
ependymal tumor
bone cancer
spinal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7497 DOID:7497]

|

|

|

|-

| brain germinoma

| class of disease

| brain cancer
central nervous system germinoma
germ cell cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2127 DOID:2127]

|

|

|

|-

| brain glioblastoma multiforme

| class of disease

| brain glioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3073 DOID:3073]

|

|

|

|-

| brain glioma

| class of disease

| brain cancer
glioma

| brain cancer that has material basis in glial cells

| [http://www.disease-ontology.org/?id=DOID:0060108 DOID:0060108]

|

| Brain gliomas

|

|-

| brain infarction

| class of disease

| cerebrovascular disease
brain ischemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3454 DOID:3454]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.150.477 C10.228.140.300.150.477]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.775.200 C10.228.140.300.775.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.092.477 C14.907.253.092.477]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.855.200 C14.907.253.855.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.513.355.250 C23.550.513.355.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.717.489.250 C23.550.717.489.250]

|

|

|-

| brain ischemia

| class of disease

| ischemia
cerebrovascular disease
stroke
disease

| insufficient blood flow to the brain

| [http://www.disease-ontology.org/?id=DOID:2316 DOID:2316]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.150 C10.228.140.300.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.092 C14.907.253.092]

| Brain ischemia

|

|-

| brain meningioma

| class of disease

| brain cancer
meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060106 DOID:0060106]

|

|

|

|-

| brain oligodendroglioma

| class of disease

| brain glioma
oligodendroglioma

| brain glioma that has material basis in oligodendrocytes

| [http://www.disease-ontology.org/?id=DOID:3187 DOID:3187]

|

|

|

|-

| brain sarcoma

| class of disease

| brain cancer
central nervous system sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2132 DOID:2132]

|

|

|

|-

| brain small vessel disease

| class of disease

| encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112313 DOID:0112313]

|

|

|

|-

| brain small vessel disease 3

| class of disease

| brain small vessel disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112315 DOID:0112315]

|

|

|

|-

| brain stem angioblastoma

| class of disease

| brain stem cancer
hemangioblastoma
benign neoplasm of brain stem
carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6501 DOID:6501]

|

|

|

|-

| brain stem astrocytic neoplasm

| class of disease

| Brainstem glioma
brain astrocytoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4860 DOID:4860]

|

|

|

|-

| brain stem cancer

| class of disease

| infratentorial cancer
brain stem neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4203 DOID:4203]

|

|

|

|-

| brain stem ependymoma

| class of disease

| Brainstem glioma
brain ependymoma
ependymal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5508 DOID:5508]

|

|

|

|-

| brain stem infarction

| class of disease

| brain infarction
brain stem stroke syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:3523 DOID:3523]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.150.477.100 C10.228.140.300.150.477.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.775.200.100 C10.228.140.300.775.200.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.092.477.100 C14.907.253.092.477.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.855.200.100 C14.907.253.855.200.100]

|

|

|-

| brain stem medulloblastoma

| class of disease

| brain stem cancer
medulloblastoma

| brain stem cancer that begins in the lower part of the brain on the floor of the skull

| [http://www.disease-ontology.org/?id=DOID:0050899 DOID:0050899]

|

|

|

|-

| brainstem intraparenchymal clear cell meningioma

| class of disease

| clear cell meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4209 DOID:4209]

|

|

|

|-

| branch retinal artery occlusion

| class of disease

| retinal artery occlusion

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13094 DOID:13094]

|

|

|

|-

| branchiootorenal syndrome 1

| class of disease

| branchiootorenal syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111423 DOID:0111423]

|

|

|

|-

| branchiootorenal syndrome 2

| class of disease

| branchiootorenal syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111424 DOID:0111424]

|

|

|

|-

| brawny scleritis

| class of disease

| anterior scleritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14287 DOID:14287]

|

|

|

|-

| breast adenocarcinoma

| class of disease

| breast carcinoma
adenocarcinoma

| breast carcinoma that originates in the milk ducts and/or lobules (glandular tissue) of the breast

| [http://www.disease-ontology.org/?id=DOID:3458 DOID:3458]

|

|

|

|-

| breast adenoid cystic carcinoma

| class of disease

| breast carcinoma
breast adenocarcinoma
invasive breast carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4877 DOID:4877]

|

|

|

|-

| breast adenoma

| class of disease

| breast benign neoplasm
benign neoplasms by histologic type
adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1625 DOID:1625]

|

|

|

|-

| breast adenomyoepithelial adenosis

| class of disease

| microglandular adenosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7312 DOID:7312]

|

|

|

|-

| breast adenomyoepithelioma

| class of disease

| breast myoepithelial neoplasm

| breast myoepithelial neoplasm that affects the breast and is characterized by biphasic proliferation of both epithelial and myoepithelial cells

| [http://www.disease-ontology.org/?id=DOID:1642 DOID:1642]

|

|

|

|-

| breast angiomatosis

| class of disease

| angiomatosis
capillary disease
breast disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1637 DOID:1637]

|

|

|

|-

| breast angiosarcoma

| class of disease

| breast sarcoma
inherited soft tissue tumor
inherited gynecological tumor
rare genetic vascular tumor
angiosarcoma

| angiosarcoma and sarcoma of breast and vascular neoplasm of breast that is located in the cells that line the blood vessels within the breast or underarm area

| [http://www.disease-ontology.org/?id=DOID:4511 DOID:4511]

|

|

|

|-

| breast apocrine adenoma

| class of disease

| breast adenoma
hidradenoma
benign neoplasm of sweat gland
apocrine adenoma
benign epithelial skin neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7540 DOID:7540]

|

|

|

|-

| breast apocrine carcinoma

| class of disease

| breast adenocarcinoma
apocrine adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6581 DOID:6581]

|

|

|

|-

| breast apocrine carcinoma in situ

| class of disease

| breast carcinoma in situ

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8428 DOID:8428]

|

|

|

|-

| breast benign neoplasm

| class of disease
symptom or sign

| thoracic benign neoplasm
breast disease
breast neoplasm

| non-metastasizing neoplasm arising from the breast parenchyma

| [http://www.disease-ontology.org/?id=DOID:0060082 DOID:0060082]

|

|

|

|-

| breast cancer

| class of disease
symptom or sign

| thoracic cancer
breast disease
breast neoplasm
disease

| cancer that originates in the mammary gland

| [http://www.disease-ontology.org/?id=DOID:1612 DOID:1612]

|

| Breast cancer

| File:Breast DCIS histopathology (1).jpg

|-

| breast capillary hemangioma

| class of disease

| breast hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6491 DOID:6491]

|

|

|

|-

| breast carcinoma

| class of disease

| breast cancer

| A breast cancer that has material basis in abnormally proliferating cells derives from epithelial cells.

| [http://www.disease-ontology.org/?id=DOID:3459 DOID:3459]

|

| Breast carcinomas

|

|-

| breast carcinoma in situ

| class of disease

| in situ carcinoma
carcinoma in situ of breast and genitourinary system
breast disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8791 DOID:8791]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.240.187 C04.557.470.200.240.187]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.180.130 C04.588.180.130]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.090.500.130 C17.800.090.500.130]

|

|

|-

| breast columnar cell mucinous carcinoma

| class of disease

| breast mucinous carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8130 DOID:8130]

|

|

|

|-

| breast cystic hypersecretory carcinoma

| class of disease

| breast secretory carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7537 DOID:7537]

|

|

|

|-

| breast disease

| class of disease

| thoracic disease
disease

| thoracic disease that is located in the breast

| [http://www.disease-ontology.org/?id=DOID:3463 DOID:3463]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.090 C17.800.090]

| Diseases and disorders of the breast

|

|-

| breast duct papilloma

| class of disease

| intraductal papillary breast neoplasm
papilloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1626 DOID:1626]

|

|

|

|-

| breast ductal adenoma

| class of disease

| breast adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7538 DOID:7538]
[http://www.disease-ontology.org/?id=DOID:5397 DOID:5397]

|

|

|

|-

| breast ductal carcinoma

| class of disease

| breast carcinoma
ductal carcinoma

| breast carcinoma that derives from the lining of milk ducts

| [http://www.disease-ontology.org/?id=DOID:3007 DOID:3007]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.232.500 C04.557.470.200.025.232.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.615.132.500 C04.557.470.615.132.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.180.390 C04.588.180.390]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.090.500.390 C17.800.090.500.390]

| Breast ductal carcinomas

|

|-

| breast epithelioid hemangioma

| class of disease

| breast hemangioma
histiocytoid hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6492 DOID:6492]

|

|

|

|-

| breast fibroadenoma

| class of disease

| breast benign neoplasm
adenoma
disease

| breast benign neoplasm comprised of fibrous and glandular tissues

| [http://www.disease-ontology.org/?id=DOID:1618 DOID:1618]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.590.595.350 C04.557.450.565.590.595.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.625.350 C04.557.470.625.350]

| Breast fibroadenomas

| File:Breast fibradenoma (1).jpg

|-

| breast fibrocystic disease

| class of disease
symptom or sign

| breast benign neoplasm
benign mammary dysplasia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10354 DOID:10354]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.090.750 C17.800.090.750]

| Fibrocystic breast changes

|

|-

| breast fibrosarcoma

| class of disease

| breast sarcoma
fibrosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6001 DOID:6001]

|

|

|

|-

| breast giant fibroadenoma

| class of disease

| breast fibroadenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7223 DOID:7223]

|

|

|

|-

| breast granular cell tumor

| class of disease

| breast cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3011 DOID:3011]

|

|

|

|-

| breast hemangioma

| class of disease

| breast benign neoplasm
hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:476 DOID:476]

|

|

|

|-

| breast hemangiopericytoma

| class of disease

| breast sarcoma
hemangiopericytoma

| hemangiopericytoma that is manifested in the breast

| [http://www.disease-ontology.org/?id=DOID:5370 DOID:5370]

|

|

|

|-

| breast implant-associated anaplastic large cell lymphoma

| class of disease

| peripheral T-cell lymphoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070333 DOID:0070333]

|

|

|

|-

| breast intracanalicular fibroadenoma

| class of disease

| breast fibroadenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2656 DOID:2656]

|

|

|

|-

| breast intraductal papillomatosis

| class of disease

| breast papillomatosis
intraductal papillomatosis
intraductal breast papilloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7511 DOID:7511]

|

|

|

|-

| breast intraductal proliferative lesion

| class of disease

| intraductal breast neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6839 DOID:6839]

|

|

|

|-

| breast juvenile papillomatosis

| class of disease

| breast papillomatosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6641 DOID:6641]

|

|

|

|-

| breast large cell neuroendocrine carcinoma

| class of disease

| inherited gynecological tumor
rare genetic respiratory disease
inherited neuroendocrine tumor
invasive breast carcinoma
breast carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6657 DOID:6657]

|

|

|

|-

| breast leiomyoma

| class of disease

| breast benign neoplasm
leiomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1623 DOID:1623]

|

|

|

|-

| breast leiomyosarcoma

| class of disease

| breast sarcoma
inherited gynecological tumor
inherited soft tissue tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5285 DOID:5285]

|

|

|

|-

| breast liposarcoma

| class of disease

| breast sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5701 DOID:5701]

|

|

|

|-

| breast lobular carcinoma

| class of disease

| breast carcinoma
Lobular carcinoma

| breast carcinoma that derives from breast lobules (milk glands)

| [http://www.disease-ontology.org/?id=DOID:0050938 DOID:0050938]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.305 C04.557.470.200.025.305]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.615.305 C04.557.470.615.305]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.180.437 C04.588.180.437]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.090.500.437 C17.800.090.500.437]

|

|

|-

| breast lymphoma

| class of disease

| breast cancer
inherited gynecological tumor
genetic hematologic disease
lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5826 DOID:5826]

|

|

|

|-

| breast malignant eccrine spiradenoma

| class of disease

| breast cancer
inherited gynecological tumor
inherited skin tumor
genetic epidermal disorder
malignant spiradenoma
breast adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7983 DOID:7983]

|

|

|

|-

| breast malignant phyllodes tumor

| class of disease

| breast cancer
breast fibroepithelial neoplasm
phyllodes tumor
malignant phyllodes tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3016 DOID:3016]

|

|

|

|-

| breast medullary carcinoma

| class of disease

| breast adenocarcinoma
invasive ductal carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5605 DOID:5605]

|

|

|

|-

| breast metaplastic carcinoma

| class of disease

| breast carcinoma
Metaplastic carcinoma
invasive breast carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4680 DOID:4680]

|

|

|

|-

| breast mucinous carcinoma

| class of disease

| breast adenocarcinoma
invasive ductal carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3610 DOID:3610]

|

| Mucinous breast carcinoma

|

|-

| breast mucinous cystadenocarcinoma

| class of disease

| breast mucinous carcinoma
mucinous cystadenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3609 DOID:3609]

|

|

|

|-

| breast mucoepidermoid carcinoma

| class of disease

| breast metaplastic carcinoma
breast adenocarcinoma
mucoepidermoid carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4679 DOID:4679]

|

|

|

|-

| breast myoepithelial carcinoma

| class of disease

| breast carcinoma
invasive breast carcinoma
myoepithelial carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6776 DOID:6776]

|

|

|

|-

| breast myoepithelial neoplasm

| class of disease

| breast cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3004 DOID:3004]

|

|

|

|-

| breast myoepitheliosis

| class of disease

| breast myoepithelial neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7521 DOID:7521]

|

|

|

|-

| breast neuroendocrine neoplasm

| class of disease

| breast benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3009 DOID:3009]

|

|

|

|-

| breast osteosarcoma

| class of disease

| breast sarcoma
extraosseous osteosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7787 DOID:7787]

|

|

|

|-

| breast papillary carcinoma

| class of disease

| breast carcinoma
breast papillary neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5592 DOID:5592]

|

|

|

|-

| breast papillomatosis

| class of disease

| breast benign neoplasm
papillomatosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1634 DOID:1634]

|

|

|

|-

| breast pericanalicular fibroadenoma

| class of disease

| breast fibroadenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2639 DOID:2639]

|

|

|

|-

| breast rhabdomyosarcoma

| class of disease

| breast sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4060 DOID:4060]

|

|

|

|-

| breast sarcoma

| class of disease

| breast cancer

| breast cancer that has material basis in abnormally proliferating cells derives from mesenchymal cells

| [http://www.disease-ontology.org/?id=DOID:3017 DOID:3017]

|

|

|

|-

| breast scirrhous carcinoma

| class of disease

| breast carcinoma
invasive ductal carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7578 DOID:7578]

|

|

|

|-

| breast secretory carcinoma

| class of disease

| breast adenocarcinoma
invasive ductal carcinoma
secretory carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4922 DOID:4922]

|

|

|

|-

| breast signet ring cell adenocarcinoma

| class of disease

| breast adenocarcinoma
signet ring cell adenocarcinoma
invasive breast carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3503 DOID:3503]

|

|

|

|-

| breast squamous cell carcinoma

| class of disease

| breast metaplastic carcinoma
squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5514 DOID:5514]

|

|

|

|-

| brittle cornea syndrome 2

| class of disease

| autosomal recessive disease
corneal disease
Ehlers-Danlos syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080729 DOID:0080729]

|

|

|

|-

| broad ligament malignant neoplasm

| class of disease

| uterine adnexa cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10744 DOID:10744]

|

|

|

|-

| bronchial mucus gland adenoma

| class of disease

| bronchus adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7030 DOID:7030]

|

|

|

|-

| bronchial neoplasm

| class of disease

| respiratory system benign neoplasm
bronchospasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:3906 DOID:3906]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.894.797.520.109 C04.588.894.797.520.109]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.127.265 C08.127.265]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.785.520.100 C08.785.520.100]

|

|

|-

| bronchiectasis 1

| class of disease

| bronchiectasis
autosomal dominant disease

| bronchiectasis that has material basis in mutation in the gene encoding the beta subunit of the epithelial sodium channel on chromosome 16p12

| [http://www.disease-ontology.org/?id=DOID:0080526 DOID:0080526]

|

|

|

|-

| bronchiectasis 2

| class of disease

| autosomal dominant disease
bronchiectasis

| bronchiectasis that has material basis in mutation in the gene encoding the alpha subunit of the epithelial sodium channel

| [http://www.disease-ontology.org/?id=DOID:0080527 DOID:0080527]

|

|

|

|-

| bronchiectasis 3

| class of disease

| autosomal dominant disease
bronchiectasis

| bronchiectasis that has material basis in mutation in the gene encoding the gamma subunit of the epithelial sodium channel

| [http://www.disease-ontology.org/?id=DOID:0080528 DOID:0080528]

|

|

|

|-

| bronchiolitis

| class of disease
symptom or sign

| lung disease
bronchospasm
respiratory syncytial virus infectious disease
respiratory signs and symptoms
disease

| blockage of the small airways in the lungs due to a viral infection

| [http://www.disease-ontology.org/?id=DOID:2942 DOID:2942]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.127.446.135 C08.127.446.135]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.495.146.135 C08.381.495.146.135]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.730.099.135 C08.730.099.135]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.748.099.135 C01.748.099.135]

| Bronchiolitis

| File:Bronchiolitis chest X-ray.jpg

|-

| bronchiolo-alveolar adenocarcinoma

| class of disease

| adenocarcinoma of the lung

| lung adenocarcinoma characterized by a predominantly lepidic pattern and 5 mm or less invasion in greatest dimension

| [http://www.disease-ontology.org/?id=DOID:4926 DOID:4926]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.022.500 C04.557.470.200.025.022.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.894.797.520.055.500 C04.588.894.797.520.055.500]

| Bronchiolo-alveolar carcinoma

|

|-

| bronchitis

| class of disease
symptom or sign

| bronchospasm
chronic obstructive pulmonary disease
respiratory signs and symptoms
disease

| inflammation of the large airways in the lungs

| [http://www.disease-ontology.org/?id=DOID:6132 DOID:6132]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.127.446 C08.127.446]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.495.146 C08.381.495.146]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.730.099 C08.730.099]

| Bronchitis

| File:Acute-bronchitis.jpg

|-

| bronchospasm

| class of disease

| lower respiratory tract disease
bronchial disease
disease

| lower respiratory tract disease that affects the airways leading into the lungs

| [http://www.disease-ontology.org/?id=DOID:1176 DOID:1176]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.127.321 C08.127.321]

|

|

|-

| bronchus adenoma

| class of disease

| lung adenoma
bronchial neoplasm
respiratory tract papilloma
benign neoplasms by histologic type
adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5391 DOID:5391]

|

|

|

|-

| bronchus cancer

| class of disease

| respiratory system cancer
lung cancer
bronchospasm

| respiratory system cancer that is located in the bronchus

| [http://www.disease-ontology.org/?id=DOID:1325 DOID:1325]

|

|

|

|-

| bronchus carcinoma

| class of disease

| bronchus cancer
carcinoma

| bronchus cancer that has material basis in epithelial cells

| [http://www.disease-ontology.org/?id=DOID:3904 DOID:3904]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.894.797.520.109.220 C04.588.894.797.520.109.220]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.540.140 C08.381.540.140]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.785.520.100.220 C08.785.520.100.220]

|

|

|-

| brown shrimp allergy

| class of disease

| shrimp allergy
crustacean allergy

| crustacean allergy triggered by Farfantepenaeus aztecus

| [http://www.disease-ontology.org/?id=DOID:0060525 DOID:0060525]

|

|

|

|-

| bruxism

| class of disease
symptom or sign

| sleep disorder
parafunctional habit
disease

| disorder that involves involuntarily grinding or clenching of the teeth

| [http://www.disease-ontology.org/?id=DOID:2846 DOID:2846]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.793.099 C07.793.099]

| Bruxism

| File:Deviated midline 2.JPG

|-

| bubonic plague

| class of disease

| plague
lymph node disease
disease

| human and animal disease

| [http://www.disease-ontology.org/?id=DOID:10773 DOID:10773]

|

| Bubonic plague

| File:Yersinia pestis.jpg

|-

| bulbomembranous urethral cancer

| class of disease

| male urethral cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8259 DOID:8259]

|

|

|

|-

| bulbospinal polio

| class of disease

| paralytic poliomyelitis
spinal cord disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050514 DOID:0050514]

|

|

|

|-

| bullous keratopathy

| class of disease

| corneal edema
keratopathy
cornea blistering

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11031 DOID:11031]

|

|

|

|-

| bullous pemphigoid

| class of disease

| autoimmune skin disease
pemphigoid
bullous skin disease
disease

| autoimmune disease of skin and connective tissue characterized by large blisters

| [http://www.disease-ontology.org/?id=DOID:8506 DOID:8506]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.865.690 C17.800.865.690]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.730 C20.111.730]

| Bullous pemphigoid

| File:Bullous pemphgoid in a 72 year old bedridden female2.JPG

|-

| bullous retinoschisis

| class of disease

| retinoschisis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12108 DOID:12108]

|

|

|

|-

| bullous skin disease

| class of disease

| dermatitis
cellulitis
autoimmune skin disease
connective tissue disease

| An autoimmune disease of skin and connective tissue that is characterized by blisters filled with a watery fluid, located in skin. The disease is associated with the amount of gluten ingested.

| [http://www.disease-ontology.org/?id=DOID:8502 DOID:8502]

|

|

|

|-

| buphthalmos

| class of disease

| hydrophthalmos
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11211 DOID:11211]

|

| Buphthalmos

|

|-

| burning mouth syndrome

| class of disease
symptom or sign

| mouth disease
dysesthesia
glossalgia
rare headache disorder
burning sensation
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4331 DOID:4331]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.114 C07.465.114]

| Burning mouth syndrome

|

|-

| bursitis

| class of disease
symptom or sign

| arthropathy
synovial, tendon or bursa disorder
inflammation
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:2965 DOID:2965]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.550.251 C05.550.251]

| Bursitis

| File:Bursitis Elbow WC.JPG

|-

| byssinosis

| class of disease

| pneumoconiosis
disease

| human disease of the respiratory system

| [http://www.disease-ontology.org/?id=DOID:10323 DOID:10323]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.483.581.275 C08.381.483.581.275]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C24.800.323 C24.800.323]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.520.702.275 C08.381.520.702.275]

|

|

|-

| calcaneal spur

| class of disease

| osteophyte
foot diseases
exostosis

| exostosis that results in an abnomal growth located in calcaneus

| [http://www.disease-ontology.org/?id=DOID:210 DOID:210]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.540.310.600 C05.116.540.310.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.360.400 C05.360.400]

| Calcaneal spur

| File:2023 Ostroga piętowa.jpg

|-

| calcaneonavicular coalition

| class of disease

| synostosis
tarsal-carpal coalition syndrome

| synostosis characterized by the fusion of carpal and tarsal bones, which causes stiffness and immobility of the hands and the feet

| [http://www.disease-ontology.org/?id=DOID:14762 DOID:14762]

|

|

|

|-

| calcific tendinitis

| class of disease

| tendinitis
calcium deposits in tendon and bursa

| disorder characterized by deposits of hydroxyapatite (a crystalline calcium phosphate) in any tendon of the body

| [http://www.disease-ontology.org/?id=DOID:14181 DOID:14181]

|

| Calcific tendinitis

|

|-

| calcinosis

| class of disease

| calcium metabolism disease
ectopic calcification
disease

| calcium metabolism disease that is the result of the formation of calcium deposits in any soft tissue

| [http://www.disease-ontology.org/?id=DOID:182 DOID:182]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.174.130 C18.452.174.130]

| Calcinosis

|

|-

| calciphylaxis

| class of disease

| calcinosis
systemic disease
vascular disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4734 DOID:4734]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.174.130.186 C18.452.174.130.186]

| Calciphylaxis

| File:Calciphylaxis.png

|-

| calcium metabolism disease

| class of disease

| mineral metabolism disease

| Disorders in the processing of calcium in the body: its absorption, transport, storage, and utilization

| [http://www.disease-ontology.org/?id=DOID:10575 DOID:10575]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.174 C18.452.174]

|

| File:Ca-TableImage.svg

|-

| calcium oxalate nephrolithiasis

| class of disease

| nephrolithiasis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080652 DOID:0080652]

|

|

|

|-

| cancer

| class of disease

| disease of cellular proliferation
neoplasm
tumor
disease

| group of diseases involving abnormal cell growth and spread

| [http://www.disease-ontology.org/?id=DOID:162 DOID:162]

|

|

| File:Breast cancer cell (2).jpg

|-

| cancer of exocrine pancreas

| class of disease

| pancreatic cancer
pancreatic exocrine neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1795 DOID:1795]

|

|

|

|-

| cancerophobia

| class of disease

| nosophobia

| overwhelming, irrational, and persistent fear of being diagnosed with cancer

| [http://www.disease-ontology.org/?id=DOID:602 DOID:602]

|

|

|

|-

| candidal paronychia

| class of disease

| candidiasis
paronychia
nail disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14512 DOID:14512]

|

|

|

|-

| cannabis abuse

| class of disease

| substance abuse
effects of cannabis
cannabis consumption

| substance abuse that involves the recurring use of cannabis despite negative consequences

| [http://www.disease-ontology.org/?id=DOID:9505 DOID:9505]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.775.635 C25.775.635]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.900.635 F03.900.635]

|

|

|-

| cannabis dependence

| class of disease

| hallucinogen dependence
effects of cannabis

| drug dependence that involves the continued use of cannabis despite problems related to use of the substance

| [http://www.disease-ontology.org/?id=DOID:1849 DOID:1849]

|

|

|

|-

| capillariasis

| class of disease

| parasitic helminthiasis infectious disease
intestinal disease
liver disease
lung disease
disease

| disease caused by nematodes of the genus Capillaria

| [http://www.disease-ontology.org/?id=DOID:12474 DOID:12474]

|

|

|

|-

| capillary disease

| class of disease

| vascular disease
microangiopathy

| vascular disease that is located in the capillaries

| [http://www.disease-ontology.org/?id=DOID:1271 DOID:1271]

|

|

|

|-

| capillary hemangioma

| class of disease
symptom or sign

| capillary disease
skin hemangioma

| most common variant of hemangioma, dull red, firm, dome-shaped hemangioma, usually located on the head and neck, which grows rapidly caused by proliferation of immature capillary vessels

| [http://www.disease-ontology.org/?id=DOID:2725 DOID:2725]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.645.375.380 C04.557.645.375.380]

| Cutaneous capillary hemangioma

| File:Capillary haemangioma.jpg

|-

| capillary leak syndrome

| class of disease

| capillary disease
urticarial syndrome
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:14400 DOID:14400]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.218 C14.907.218]

|

|

|-

| capillary lymphangioma

| class of disease

| capillary disease
lymphangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2286 DOID:2286]

|

|

|

|-

| carbamazepine allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger carbamazepine

| [http://www.disease-ontology.org/?id=DOID:0040006 DOID:0040006]

|

|

|

|-

| carbapenem allergy

| class of disease

| drug allergy
beta-lactam allergy

| drug allergy that has allergic trigger carbapenems

| [http://www.disease-ontology.org/?id=DOID:0040032 DOID:0040032]

|

|

|

|-

| carbohydrate metabolic disorder

| class of disease

| inherited metabolic disorder
carbohydrate metabolism disease

| inherited metabolic disorder that affect the catabolism and anabolism of carbohydrates

| [http://www.disease-ontology.org/?id=DOID:2978 DOID:2978]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.202 C16.320.565.202]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.202 C18.452.648.202]

| Disorders of carbohydrate metabolism

|

|-

| carbohydrate metabolism disease

| class of disease

| acquired metabolic disease

| acquired metabolic disease that is characterized by abnormal carbohydrate metabolism

| [http://www.disease-ontology.org/?id=DOID:0050013 DOID:0050013]

|

|

|

|-

| carbuncle

| class of disease
гнійне захворювання

| pyoderma

| human disease

| [http://www.disease-ontology.org/?id=DOID:2176 DOID:2176]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.410.868.951.270.200 C01.150.252.410.868.951.270.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.819.770.270.200 C01.150.252.819.770.270.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.800.720.770.270.200 C01.800.720.770.270.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.838.765.770.270.200 C17.800.838.765.770.270.200]

| Carbuncles

| File:Carbuncle on buttok.JPG

|-

| carcinoma of supraglottis

| class of disease

| supraglottis cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7763 DOID:7763]

|

|

|

|-

| carcinosarcoma

| class of disease

| malignant mixed tumor
disease

| mixed cell type cancer that has material basis in carcinomatous (epithelial tissue) and sarcomatous (connective tissue) components

| [http://www.disease-ontology.org/?id=DOID:4236 DOID:4236]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.435.290 C04.557.435.290]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.290 C04.557.450.795.290]

| Carcinosarcoma

|

|-

| cardia cancer

| class of disease

| stomach cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:10548 DOID:10548]

|

|

|

|-

| cardiac granular cell neoplasm

| class of disease

| cardiovascular organ benign neoplasm
benign neoplasm of epicardium

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5044 DOID:5044]

|

|

|

|-

| cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies

| class of disease

| genetic disease
genetic syndromic intellectual disability
rare syndrome with cardiac malformations
syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111697 DOID:0111697]

|

|

|

|-

| cardiac sarcoidosis

| class of disease

| sarcoidosis
heart disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13405 DOID:13405]

|

|

|

|-

| cardiac tuberculosis

| class of disease

| cardiovascular tuberculosis
heart disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060570 DOID:0060570]

|

|

|

|-

| cardiac valvular defect, developmental

| class of disease

| genetic disease
congenital disorder
Heart valve dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080633 DOID:0080633]

|

|

|

|-

| cardiofaciocutaneous syndrome 1

| class of disease

| autosomal dominant disease
cardiofaciocutaneous syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111460 DOID:0111460]

|

|

|

|-

| cardiofaciocutaneous syndrome 2

| class of disease

| autosomal dominant disease
cardiofaciocutaneous syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111461 DOID:0111461]

|

|

|

|-

| cardiofaciocutaneous syndrome 3

| class of disease

| cardiofaciocutaneous syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111462 DOID:0111462]

|

|

|

|-

| cardiofaciocutaneous syndrome 4

| class of disease

| cardiofaciocutaneous syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111463 DOID:0111463]

|

|

|

|-

| cardiomyopathy, infantile hypertrophic

| class of disease

| genetic disease
hypertrophic cardiomyopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111753 DOID:0111753]

|

|

|

|-

| cardiovascular organ benign neoplasm

| class of disease

| organ system benign neoplasm
cardiovascular neoplasm
cardiovascular disease

| organ system benign neoplasm disease located in the blood, heart, blood vessels or the lymphatic system

| [http://www.disease-ontology.org/?id=DOID:0060091 DOID:0060091]

|

|

|

|-

| carotenemia

| class of disease

| acquired metabolic disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9969 DOID:9969]

|

|

|

|-

| carotid artery disease

| class of disease

| cerebrovascular disease
artery disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3407 DOID:3407]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.200 C10.228.140.300.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.123 C14.907.253.123]

|

|

|-

| carotid artery dissection

| class of disease

| carotid artery disease
dissection
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9348 DOID:9348]

|

|

| File:Gray513.png

|-

| carotid artery occlusion

| class of disease

| occlusion precerebral artery
carotid artery stenosis
carotid artery disease
Vascular occlusion

| human disease

| [http://www.disease-ontology.org/?id=DOID:807 DOID:807]

|

|

|

|-

| carotid artery stenosis

| class of disease

| carotid artery disease
peripheral artery disease

| narrowing or constriction of the inner surface (lumen) of the carotid artery, usually caused by atherosclerosis

| [http://www.disease-ontology.org/?id=DOID:13001 DOID:13001]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.200.360 C10.228.140.300.200.360]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.137.230 C14.907.137.230]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.123.360 C14.907.253.123.360]

| Carotid artery stenosis

| File:Gray513.png

|-

| carotid artery thrombosis

| class of disease

| carotid artery disease
intracranial thrombosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3410 DOID:3410]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.200.355 C10.228.140.300.200.355]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.123.355 C14.907.253.123.355]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.566.206 C14.907.253.566.206]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.355.590.213.206 C14.907.355.590.213.206]

|

|

|-

| carp allergy

| class of disease

| fish allergy

| fish allergy triggered by Cyprinus carpio

| [http://www.disease-ontology.org/?id=DOID:0060516 DOID:0060516]

|

|

|

|-

| cartilage cancer

| class of disease

| connective tissue neoplasm
chondropathy
cartilage tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060102 DOID:0060102]

|

|

|

|-

| carvone allergic contact dermatitis

| class of disease

| allergic contact dermatitis

| allergic contact dermatitis that has allergic trigger (-)-carvone

| [http://www.disease-ontology.org/?id=DOID:0040064 DOID:0040064]

|

|

|

|-

| cascade stomach

| class of disease

| stomach disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12234 DOID:12234]

|

|

|

|-

| cataract 1 multiple types

| class of disease

| cataract
autosomal dominant disease

| cataract that has material basis in heterozygous mutation in the gene encoding the alpha-8 subunit of the gap junction protein (GJA8) on chromosome 1q21

| [http://www.disease-ontology.org/?id=DOID:0110231 DOID:0110231]

|

|

|

|-

| cataract 24

| class of disease

| cataract
autosomal dominant disease

| cataract that has material basis in variation in the region 17p13

| [http://www.disease-ontology.org/?id=DOID:0110257 DOID:0110257]

|

|

|

|-

| cataract 26 multiple types

| class of disease

| cataract

| cataract that has material basis in variation in the region 9q13-q22

| [http://www.disease-ontology.org/?id=DOID:0110246 DOID:0110246]

|

|

|

|-

| cataract 27

| class of disease

| cataract

| cataract that has material basis in mutation in the region 2p12

| [http://www.disease-ontology.org/?id=DOID:0110233 DOID:0110233]

|

|

|

|-

| cataract 28

| class of disease

| cataract

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110244 DOID:0110244]

|

|

|

|-

| cataract 29

| class of disease

| cataract
autosomal dominant disease

| cataract that has material basis in variation in the region 2pter-p24

| [http://www.disease-ontology.org/?id=DOID:0110232 DOID:0110232]

|

|

|

|-

| cataract 3 multiple types

| class of disease

| cataract
autosomal dominant disease

| cataract that has material basis in heterozygous mutation in the beta-B2-crystallin gene (CRYBB2) on chromosome 22q11

| [http://www.disease-ontology.org/?id=DOID:0110269 DOID:0110269]

|

|

|

|-

| cataract 37

| class of disease

| cataract
autosomal dominant disease

| A cataract that has material basis in variation in the region 12q24.2-q24.3.

| [http://www.disease-ontology.org/?id=DOID:0110252 DOID:0110252]

|

|

|

|-

| cataract 4 multiple types

| class of disease

| cataract
autosomal dominant disease

| cataract that has material basis in heterozygous mutation in the gamma-D-crystallin gene (CRYGD) on chromosome 2q33

| [http://www.disease-ontology.org/?id=DOID:0110234 DOID:0110234]

|

|

|

|-

| cataract 47

| class of disease

| autosomal dominant disease
cataract

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070353 DOID:0070353]

|

|

|

|-

| cataract 48

| class of disease

| cataract
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070354 DOID:0070354]

|

|

|

|-

| cataract 9 multiple types

| class of disease

| cataract
autosomal recessive disease
autosomal dominant disease

| cataract that has material basis in heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22

| [http://www.disease-ontology.org/?id=DOID:0110266 DOID:0110266]

|

|

|

|-

| catecholaminergic polymorphic ventricular tachycardia 1

| class of disease

| catecholaminergic polymorphic ventricular tachycardia

| catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal dominant inheritance and has material basis in heterozygous mutation in the RYR2 gene on chromosome 1q43

| [http://www.disease-ontology.org/?id=DOID:0060675 DOID:0060675]

|

|

|

|-

| cauda equina intradural extramedullary astrocytoma

| class of disease

| cauda equina neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4846 DOID:4846]

|

|

|

|-

| cauda equina neoplasm

| class of disease

| spinal cord neoplasm
nerve root neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4847 DOID:4847]

|

|

|

|-

| cauda equina syndrome

| class of disease

| peripheral neuropathy
syndrome
disease

| nerve damage at the end of the spinal cord

| [http://www.disease-ontology.org/?id=DOID:11577 DOID:11577]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.550.350 C10.668.829.550.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.800.750.150 C10.668.829.800.750.150]

| Cauda equina syndrome

| File:MRI of the lumbar spine with abscess in the posterior epidural space, causing cauda equina syndrome.jpg

|-

| causalgia

| class of disease

| complex regional pain syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:3222 DOID:3222]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.177.195.200 C10.177.195.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.250.200 C10.668.829.250.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.600.200 C10.668.829.600.200]

|

|

|-

| cavernous hemangioma

| class of disease
symptom or sign

| vascular hemostatic disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:483 DOID:483]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.645.375.385 C04.557.645.375.385]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.454.385 C14.907.454.385]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463.515.385 C15.378.463.515.385]

| Cavernous hemangiomas

|

|-

| cavernous hemangioma of orbit

| class of disease

| cavernous hemangioma
hemangioma of orbit

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14463 DOID:14463]

|

|

|

|-

| cavernous sinus thrombosis

| class of disease

| cerebral venous sinus thrombosis
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3575 DOID:3575]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.525.425.500.375 C10.228.140.300.525.425.500.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.566.350.500.375 C14.907.253.566.350.500.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.355.590.213.350.500.375 C14.907.355.590.213.350.500.375]

|

| File:Gray571.png

|-

| cecal disease

| class of disease

| intestinal disease

| intestinal disease located in the cecum

| [http://www.disease-ontology.org/?id=DOID:1518 DOID:1518]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.110 C06.405.469.110]

|

|

|-

| cecum adenoma

| class of disease

| cecal benign neoplasm
benign neoplasms by histologic type
adenoma

| cecal benign neoplasm that has material basis in epithelial tissue with glandular origin

| [http://www.disease-ontology.org/?id=DOID:0050910 DOID:0050910]

|

|

|

|-

| cecum cancer

| class of disease

| large intestine cancer
cecal neoplasm
cecal disease

| large intestine cancer that is located in the cecum

| [http://www.disease-ontology.org/?id=DOID:1521 DOID:1521]

|

|

|

|-

| cecum lymphoma

| class of disease

| cecum cancer
lymphoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:1522 DOID:1522]

|

|

|

|-

| cefaclor allergy

| class of disease

| cephalosporin allergy

| cephalosporin allergy that has allergic trigger cefaclor

| [http://www.disease-ontology.org/?id=DOID:0040023 DOID:0040023]

|

|

|

|-

| cefixime allergy

| class of disease

| cephalosporin allergy

| cephalosporin allergy that has allergic trigger cefixime

| [http://www.disease-ontology.org/?id=DOID:0040030 DOID:0040030]

|

|

|

|-

| cefotaxime allergy

| class of disease

| cephalosporin allergy

| cephalosporin allergy that has allergic trigger cefotaxime

| [http://www.disease-ontology.org/?id=DOID:0040020 DOID:0040020]

|

|

|

|-

| cefotiam allergy

| class of disease

| cephalosporin allergy

| cephalosporin allergy that has allergic trigger cefotiam

| [http://www.disease-ontology.org/?id=DOID:0040103 DOID:0040103]

|

|

|

|-

| ceftazidime allergy

| class of disease

| cephalosporin allergy

| cephalosporin allergy that has allergic trigger ceftazidime

| [http://www.disease-ontology.org/?id=DOID:0040024 DOID:0040024]

|

|

|

|-

| ceftriaxone allergy

| class of disease

| cephalosporin allergy

| cephalosporin allergy that has allergic trigger ceftriaxone

| [http://www.disease-ontology.org/?id=DOID:0040005 DOID:0040005]

|

|

|

|-

| cefuroxime allergy

| class of disease

| cephalosporin allergy

| cephalosporin allergy that has allergic trigger cefuroxime

| [http://www.disease-ontology.org/?id=DOID:0040025 DOID:0040025]

|

|

|

|-

| celery allergy

| class of disease

| vegetable allergy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070335 DOID:0070335]

|

|

|

|-

| celiac disease

| class of disease
symptom or sign

| autoimmune disease of gastrointestinal tract
gluten-related disorder
disease

| long term autoimmune disorder caused by a reaction to gluten

| [http://www.disease-ontology.org/?id=DOID:10608 DOID:10608]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.637.250 C06.405.469.637.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.603.250 C18.452.603.250]

| Coeliac disease

| File:Coeliac path.jpg

|-

| cell type cancer

| class of disease

| cancer

| cancer that is classified by the type of cell from which it is derived

| [http://www.disease-ontology.org/?id=DOID:0050687 DOID:0050687]

|

| Cancers by histological type

|

|-

| cellular congenital mesoblastic nephroma

| class of disease

| congenital mesoblastic nephroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8082 DOID:8082]

|

|

|

|-

| cellular ependymoma

| class of disease

| benign ependymoma

| An ependymoma which shows conspicuous cellularity without a significant increase in mitotic rate. (Adapted from WHO)

| [http://www.disease-ontology.org/?id=DOID:5500 DOID:5500]

|

|

|

|-

| cellular leiomyoma

| class of disease

| leiomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5139 DOID:5139]

|

|

|

|-

| cellular myxoid liposarcoma

| class of disease

| liposarcoma
myxoid liposarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5692 DOID:5692]

|

|

|

|-

| cellular neurofibroma

| class of disease

| neurofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5152 DOID:5152]

|

|

|

|-

| cellular phase chronic idiopathic myelofibrosis

| class of disease

| myelofibrosis
chronic idiopathic myelofibrosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8106 DOID:8106]

|

|

|

|-

| cellular schwannoma

| class of disease

| neurilemmoma

| neurilemmoma with a predominantly cellular growth but no Verocay bodies

| [http://www.disease-ontology.org/?id=DOID:3196 DOID:3196]

|

|

|

|-

| central breast papilloma

| class of disease

| breast duct papilloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8224 DOID:8224]

|

|

|

|-

| central conducting lymphatic anomaly

| class of disease

| lymphatic system disease
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0081030 DOID:0081030]

|

|

|

|-

| central corneal ulcer

| class of disease

| corneal ulcer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9910 DOID:9910]

|

|

|

|-

| central epithelioid sarcoma

| class of disease

| epithelioid sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7492 DOID:7492]

|

|

|

|-

| central gyrate choroidal dystrophy

| class of disease

| partial central choroid dystrophy

| human disease

| [http://www.disease-ontology.org/?id=DOID:9820 DOID:9820]

|

|

|

|-

| central nervous system adult germ cell tumor

| class of disease

| central nervous system germ cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5349 DOID:5349]

|

|

|

|-

| central nervous system angiosarcoma

| class of disease

| central nervous system sarcoma

| central nervous system sarcoma that is located in the inner lining of blood vessels

| [http://www.disease-ontology.org/?id=DOID:4504 DOID:4504]

|

|

|

|-

| central nervous system cancer

| class of disease

| nervous system cancer
central nervous system neoplasm
central nervous system disease

| nervous system cancer that is located in the central nervous system

| [http://www.disease-ontology.org/?id=DOID:3620 DOID:3620]

|

|

|

|-

| central nervous system childhood germ cell tumor

| class of disease

| central nervous system germ cell tumor
germ cell cancer
pediatric germ cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6052 DOID:6052]

|

|

|

|-

| central nervous system chondroma

| class of disease

| chondroma
central nervous system organ benign neoplasm
soft tissue chondroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3813 DOID:3813]

|

|

|

|-

| central nervous system disease

| class of disease

| neurological disorder
nervous system disease

| nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system

| [http://www.disease-ontology.org/?id=DOID:331 DOID:331]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228 C10.228]

| Diseases and disorders of the central nervous system

|

|-

| central nervous system embryonal carcinoma

| class of disease

| central nervous system germ cell tumor
embryonal carcinoma
primary germ cell tumor of central nervous system

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7232 DOID:7232]

|

|

|

|-

| central nervous system endodermal sinus tumor

| class of disease

| central nervous system germ cell tumor
malignant mixed tumor
sarcoma
germ cell cancer
primary germ cell tumor of central nervous system

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5343 DOID:5343]

|

|

|

|-

| central nervous system fibrosarcoma

| class of disease

| central nervous system sarcoma
fibrosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6451 DOID:6451]

|

|

|

|-

| central nervous system germ cell tumor

| class of disease

| central nervous system cancer
extragonadal germ cell tumor
germ cell cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4439 DOID:4439]

|

|

|

|-

| central nervous system germinoma

| class of disease

| central nervous system germ cell tumor
germinoma
germ cell cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4438 DOID:4438]

|

|

|

|-

| central nervous system hemangioma

| class of disease

| hemangioma
central nervous system organ benign neoplasm

| hemangioma arising from the brain and spinal cord

| [http://www.disease-ontology.org/?id=DOID:501 DOID:501]

|

|

|

|-

| central nervous system hematologic cancer

| class of disease

| central nervous system cancer
hematologic cancer

| hematologic cancer and central nervous system neoplasm that is located in the central nervous system

| [http://www.disease-ontology.org/?id=DOID:5772 DOID:5772]

|

|

|

|-

| central nervous system immature teratoma

| class of disease

| central nervous system teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6019 DOID:6019]

|

|

|

|-

| central nervous system leiomyoma

| class of disease

| central nervous system organ benign neoplasm
leiomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5126 DOID:5126]

|

|

|

|-

| central nervous system leiomyosarcoma

| class of disease

| central nervous system mesenchymal non-meningothelial tumor
leiomyosarcoma
malignant central nervous system mesenchymal, non-meningothelial neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5254 DOID:5254]

|

|

|

|-

| central nervous system leukemia

| class of disease

| leukemia
central nervous system hematologic cancer
central nervous system cancer

| hematologic cancer located in the central nervous system

| [http://www.disease-ontology.org/?id=DOID:12969 DOID:12969]

|

|

|

|-

| central nervous system lipoma

| class of disease

| central nervous system organ benign neoplasm
lipoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:6293 DOID:6293]

|

|

|

|-

| central nervous system lymphoma

| class of disease

| lymphoma
central nervous system hematologic cancer

| hematologic cancer that has material basis in lymphoma located in central nervous system

| [http://www.disease-ontology.org/?id=DOID:3234 DOID:3234]

|

|

|

|-

| central nervous system mature teratoma

| class of disease

| central nervous system teratoma
mature teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6017 DOID:6017]

|

|

|

|-

| central nervous system melanocytic neoplasm

| class of disease

| central nervous system neoplasm
melanocytic tumor
central nervous system cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4955 DOID:4955]

|

|

|

|-

| central nervous system organ benign neoplasm

| class of disease

| nervous system benign neoplasm
central nervous system neoplasm
central nervous system disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060090 DOID:0060090]

|

|

|

|-

| central nervous system origin vertigo

| class of disease

| central nervous system disease
encephalopathy
vertigo

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2479 DOID:2479]

|

|

|

|-

| central nervous system osteosarcoma

| class of disease

| central nervous system mesenchymal non-meningothelial tumor
extraosseous osteosarcoma
malignant central nervous system mesenchymal, non-meningothelial neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7994 DOID:7994]

|

|

|

|-

| central nervous system primitive neuroectodermal neoplasm

| class of disease

| central nervous system cancer
neuroectodermal tumor
Embryonal tumors of the central nervous system
primitive neuroectodermal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060103 DOID:0060103]

|

| Primitive neuroectodermal tumor

|

|-

| central nervous system rhabdomyosarcoma

| class of disease

| central nervous system sarcoma
rhabdomyosarcoma
nervous system cancer
central nervous system disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4048 DOID:4048]

|

|

|

|-

| central nervous system sarcoma

| class of disease

| central nervous system cancer
sarcoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:2133 DOID:2133]

|

|

|

|-

| central nervous system teratoma

| class of disease

| central nervous system germ cell tumor
primary germ cell tumor of central nervous system
sarcoma
germ cell cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3640 DOID:3640]

|

|

|

|-

| central nervous system vasculitis

| class of disease

| vasculitis
central nervous system disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:525 DOID:525]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.114.875 C10.114.875]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.850 C10.228.140.300.850]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.946 C14.907.253.946]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.940.907 C14.907.940.907]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.258.962 C20.111.258.962]

|

|

|-

| central neurocytoma

| class of disease

| neurocytoma
cerebral ventricle cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14174 DOID:14174]

|

| Central neurocytoma

|

|-

| central pontine myelinolysis

| class of disease

| demyelinating disease
demyelinating disease of central nervous system

| demyelination disease that is characterized by severe damage to the myelin sheath of the pons' nerve cells and has symptom acute paralysis, has symptom dysphagia, and has symptom dysarthria

| [http://www.disease-ontology.org/?id=DOID:636 DOID:636]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.163.560 C10.228.140.163.560]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.314.500 C10.314.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.132.560 C18.452.132.560]

| Central pontine myelinolysis

| File:Illu pituitary pineal glands.jpg

|-

| central precocious puberty

| class of disease

| endocrine system disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112308 DOID:0112308]

|

|

|

|-

| central precocious puberty 1

| class of disease

| autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112310 DOID:0112310]

|

|

|

|-

| central pterygium

| class of disease

| progressive peripheral pterygium

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13473 DOID:13473]

|

|

|

|-

| central retinal artery occlusion

| class of disease

| retinal artery occlusion

| retinal artery occlusion characterized by blockage of blood flow through the central retinal artery

| [http://www.disease-ontology.org/?id=DOID:13098 DOID:13098]

|

| Central retinal artery occlusion

|

|-

| central retinal vein occlusion

| class of disease

| retinal vein occlusion

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2450 DOID:2450]

|

|

|

|-

| central sleep apnea

| class of disease

| sleep apnea

| sleep apnea that is characterized by a malfunction of the basic neurological controls for breathing rate and the failure to give the signal to inhale, causing the individual to miss one or more cycles of breathing

| [http://www.disease-ontology.org/?id=DOID:9220 DOID:9220]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.618.085.852.800 C08.618.085.852.800]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.886.425.800.750.800 C10.886.425.800.750.800]

|

|

|-

| centronuclear myopathy 1

| class of disease

|

| An autosomal dominant centronuclear myopathy characterized by slowly progressive muscle wasting and weakness involving mainly the limb girdle, trunk, and neck muscles that has material basis in heterozygous mutation in DNM2 on 19p13.2.

| [http://www.disease-ontology.org/?id=DOID:0111223 DOID:0111223]

|

|

|

|-

| centronuclear myopathy 2

| class of disease

| centronuclear myopathy
autosomal recessive centronuclear myopathy

| An autosomal recessive centronuclear myopathy that has material basis in homozygous or compound heterozygous mutation in BIN1 on 2q14.3.

| [http://www.disease-ontology.org/?id=DOID:0111220 DOID:0111220]

|

|

|

|-

| centronuclear myopathy 4

| class of disease

| autosomal dominant centronuclear myopathy

| An autosomal dominant centronuclear myopathy that has material basis in heterozygous mutation in CCDC78 on 16p13.3.

| [http://www.disease-ontology.org/?id=DOID:0111224 DOID:0111224]

|

|

|

|-

| centronuclear myopathy 5

| class of disease

| autosomal recessive centronuclear myopathy

| autosomal recessive centronuclear myopathy characterized by severe neonatal hypotonia, respiratory insufficiency, and difficulty feeding that has material basis in homozygous or compound heterozygous mutation in SPEG on 2q35

| [http://www.disease-ontology.org/?id=DOID:0111222 DOID:0111222]

|

|

|

|-

| centronuclear myopathy 6 with fiber-type disproportion

| class of disease

| congenital fiber-type disproportion

| A congenital fiber-type disproportion characterized by onset in infancy or early childhood of slowly progressive centronuclear myopathy that has material basis in homozygous or compound heterozygous mutation in ZAK on 2q31.1.

| [http://www.disease-ontology.org/?id=DOID:0111221 DOID:0111221]

|

|

|

|-

| centronuclear myopathy X-linked

| class of disease

| centronuclear myopathy

| centronuclear myopathy that has material basis in X-linked inheritance of mutations in MTM1 on Xq28

| [http://www.disease-ontology.org/?id=DOID:0111225 DOID:0111225]

|

|

|

|-

| cephalosporin allergy

| class of disease

| drug allergy
beta-lactam allergy

| drug allergy that has allergic trigger cephalosporin

| [http://www.disease-ontology.org/?id=DOID:0040021 DOID:0040021]

|

|

|

|-

| cercarial dermatitis

| class of disease

| schistosomiasis
skin disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:11302 DOID:11302]

|

| Schistosome cercarial dermatitis

| File:Cercarial dermatitis lower legs.jpg

|-

| cerebellar angioblastoma

| class of disease

| cerebellum cancer
hemangioblastoma
benign neoplasm of cerebellum
carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6500 DOID:6500]

|

| Cerebellar hemangioblastoma

|

|-

| cerebellar astrocytoma

| class of disease

| cerebellum cancer
brain astrocytoma
glioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4848 DOID:4848]

|

|

|

|-

| cerebellar ataxia

| class of disease

| cerebellar disease
hereditary ataxia

| cerebellar disease characterized by ataxia originating in the cerebellum.

| [http://www.disease-ontology.org/?id=DOID:0050753 DOID:0050753]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.252.190 C10.228.140.252.190]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.350.090.500 C10.597.350.090.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.350.090.200 C23.888.592.350.090.200]

| Cerebellar ataxia

|

|-

| cerebellar ataxia type 48

| class of disease

| spinocerebellar ataxia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111746 DOID:0111746]

|

|

|

|-

| cerebellar hyplasia/atrophy, epilepsy, and global developmental delay

| class of disease

| syndrome
neurodevelopmental disorder

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070339 DOID:0070339]

|

|

|

|-

| cerebellar hypoplasia

| class of disease

| neurological disorder

| rare disorder in which the cerebellum is either missing entirely or is smaller than usual

| [http://www.disease-ontology.org/?id=DOID:0070338 DOID:0070338]

|

| Cerebellar hypoplasia

|

|-

| cerebellar liponeurocytoma

| class of disease

| cerebellum cancer
neuronal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6458 DOID:6458]

|

|

| File:Cerebellar liponeurocytoma.jpg

|-

| cerebellar medulloblastoma

| class of disease

| cerebellum cancer
medulloblastoma

| cerebellum cancer that begins in the lower part of the brain on the floor of the skull

| [http://www.disease-ontology.org/?id=DOID:0060104 DOID:0060104]

|

|

| File:Cerebellar medulloblastoma (1) in adult.JPG

|-

| cerebellar vermis medulloblastoma

| class of disease

| cerebellar medulloblastoma
medulloblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3860 DOID:3860]

|

|

|

|-

| cerebellopontine angle meningioma

| class of disease

| cerebellopontine angle tumor
meningioma
brain meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6337 DOID:6337]

|

|

|

|-

| cerebellopontine angle primitive neuroectodermal

| class of disease

| cerebellopontine angle tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4787 DOID:4787]

|

|

|

|-

| cerebellopontine angle tumor

| class of disease

| brain stem neoplasm
brain stem cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3200 DOID:3200]

|

|

|

|-

| cerebellum cancer

| class of disease

| infratentorial cancer
cerebellar disease
infratentorial neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4205 DOID:4205]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.614.250.195.411.211 C04.588.614.250.195.411.211]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.211.500.200 C10.228.140.211.500.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.252.200 C10.228.140.252.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.551.240.250.400.300 C10.551.240.250.400.300]

|

|

|-

| cerebral amyloid angiopathy

| class of disease

| amyloidosis

| amyloidosis where amyloid protein progressively deposits in cerebral blood vessel walls with subsequent degenerative vascular changes

| [http://www.disease-ontology.org/?id=DOID:9246 DOID:9246]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.510.200.200 C10.228.140.300.510.200.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.560.200.200 C14.907.253.560.200.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.845.500.100 C18.452.845.500.100]

| Cerebral amyloid angiopathy

| File:Cerebral amyloid angiopathy - very high mag.jpg

|-

| cerebral angioma

| class of disease

| brain angioma
benign neoplasm of cerebrum

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6621 DOID:6621]

|

|

|

|-

| cerebral arterial disease

| class of disease

| intracranial arterial disease
artery disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3527 DOID:3527]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.510.200 C10.228.140.300.510.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.560.200 C14.907.253.560.200]

|

|

|-

| cerebral arteriovenous malformation

| class of disease

| rare genetic vascular tumor
rare nervous system tumor
central nervous system vascular malformation
rare genetic epilepsy
genetic central nervous system and retinal vascular disease
central nervous system organ benign neoplasm
hemangioma
encephalopathy
cerebrovascular disease

| arteriovenous malformation that is located in the brain

| [http://www.disease-ontology.org/?id=DOID:0060688 DOID:0060688]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.520 C10.228.140.300.520]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.500.190.500 C10.500.190.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.240.850.750.295 C14.240.850.750.295]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.240.850.875.500 C14.240.850.875.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.150.295 C14.907.150.295]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.560.400 C14.907.253.560.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.240.850.750.295 C16.131.240.850.750.295]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.240.850.875.500 C16.131.240.850.875.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.666.190.500 C16.131.666.190.500]

| Cerebral arteriovenous malformation

|

|-

| cerebral arteritis

| class of disease

| central nervous system vasculitis
cerebrovascular disease
arteritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11390 DOID:11390]

|

|

|

|-

| cerebral artery occlusion

| class of disease

| cerebral infarction
cerebrovascular disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:10127 DOID:10127]

|

|

|

|-

| cerebral atherosclerosis

| class of disease

| atherosclerosis
intracranial arteriosclerosis

| type of atherosclerosis where build-up of plaque in the blood vessels of the brain occurs

| [http://www.disease-ontology.org/?id=DOID:12720 DOID:12720]

|

|

|

|-

| cerebral cavernous angioma

| class of disease

| central nervous system cavernous hemangioma
cerebrovascular disease

| vascular anomaly of the central nervous system characterized by dilated blood-filled capillaries lacking structural support

| [http://www.disease-ontology.org/?id=DOID:0060669 DOID:0060669]

|

|

|

|-

| cerebral cavernous malformation 1

| class of disease

| cerebral cavernous angioma

| cerebral cavernous malformation that has material basis in heterozygous mutation in the KRIT1 gene on chromosome 7q21

| [http://www.disease-ontology.org/?id=DOID:0080491 DOID:0080491]

|

|

|

|-

| cerebral convexity meningioma

| class of disease

| cerebral meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6114 DOID:6114]

|

|

|

|-

| cerebral creatine deficiency syndrome

| class of disease

| amino acid metabolic disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050798 DOID:0050798]

|

|

|

|-

| cerebral degeneration

| class of disease
disease

| encephalopathy
neurodegeneration

| human disease

| [http://www.disease-ontology.org/?id=DOID:1443 DOID:1443]

|

| Cerebral atrophy

|

|-

| cerebral edema

| class of disease

| encephalopathy
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:4724 DOID:4724]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.187 C10.228.140.187]

| Cerebral edema

| File:Tumor Meningioma3.JPG

|-

| cerebral hemisphere lipoma

| class of disease

| central nervous system lipoma
benign neoplasm of cerebrum
intracranial lipoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6291 DOID:6291]

|

|

|

|-

| cerebral infarction

| class of disease

| brain infarction
disease

| type of ischemic stroke resulting from a blockage in the blood vessels supplying blood to the brain

| [http://www.disease-ontology.org/?id=DOID:3526 DOID:3526]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.150.477.200 C10.228.140.300.150.477.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.775.200.200 C10.228.140.300.775.200.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.092.477.200 C14.907.253.092.477.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.855.200.200 C14.907.253.855.200.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.513.355.250.200 C23.550.513.355.250.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.717.489.250.200 C23.550.717.489.250.200]

| Cerebral infarction

| File:Infarction.svg

|-

| cerebral lipidosis

| class of disease

| cerebral degeneration
lipid storage disease
encephalopathy
metabolic disease with dementia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10742 DOID:10742]

|

|

|

|-

| cerebral lymphoma

| class of disease

| cerebrum cancer
central nervous system lymphoma
lymphoma
central nervous system hematologic cancer

| cerebrum cancer that affects the lymph cells and derives from the brain

| [http://www.disease-ontology.org/?id=DOID:5815 DOID:5815]

|

|

|

|-

| cerebral malaria

| class of disease

| malaria

| malaria that involves neurologic damage resulting from blockage of the blood vessels, caused due to the infection of the red blood cells by Plasmodium species

| [http://www.disease-ontology.org/?id=DOID:14069 DOID:14069]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.207.205.300.500 C01.207.205.300.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.610.105.300.500 C01.610.105.300.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.610.752.530.620 C01.610.752.530.620]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.920.875.620 C01.920.875.620]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.228.205.300.500 C10.228.228.205.300.500]

| Cerebral malaria

|

|-

| cerebral meningioma

| class of disease

| cerebrum cancer
meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6112 DOID:6112]

|

|

|

|-

| cerebral neuroblastoma

| class of disease

| brain cancer
cerebrum cancer
intracranial primitive neuroectodermal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4164 DOID:4164]

|

|

|

|-

| cerebral palsy

| class of disease

| encephalopathy
cerebral degeneration
palsy
disease

| group of permanent movement disorders that appear in early childhood

| [http://www.disease-ontology.org/?id=DOID:1969 DOID:1969]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.140.254 C10.228.140.140.254]

| Cerebral palsy

| File:Gray764.png

|-

| cerebral primitive neuroectodermal tumor

| class of disease

| cerebrum cancer
primitive neuroectodermal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7398 DOID:7398]

|

|

|

|-

| cerebral sarcoidosis

| class of disease

| sarcoidosis
neurosarcoidosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13403 DOID:13403]

|

|

|

|-

| cerebral venous sinus thrombosis

| class of disease

| venous thrombosis
intracranial thrombosis
stroke
disease

| presence of acute thrombosis (a blood clot) in the dural venous sinuses, which drain blood from the brain.

| [http://www.disease-ontology.org/?id=DOID:3572 DOID:3572]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.525.425.500 C10.228.140.300.525.425.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.566.350.500 C14.907.253.566.350.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.355.590.213.350.500 C14.907.355.590.213.350.500]

| Cerebral venous sinus thrombosis

| File:MBq sinusvenenthrombose.jpg

|-

| cerebral ventricle cancer

| class of disease

| cerebrum cancer
cerebral ventricle neoplasm

| cerebrum cancer that is located in the cerebral ventricles

| [http://www.disease-ontology.org/?id=DOID:3541 DOID:3541]

|

|

|

|-

| cerebritis

| class of disease

| encephalopathy
brain inflammatory disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3431 DOID:3431]

|

|

|

|-

| cerebrooculofacioskeletal syndrome

| class of disease

| Cockayne syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080910 DOID:0080910]

|

|

|

|-

| cerebrooculofacioskeletal syndrome 1

| class of disease

|

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080911 DOID:0080911]

|

|

|

|-

| cerebrovascular benign neoplasm

| class of disease

| cardiovascular organ benign neoplasm
cerebrovascular disease

| cardiovascular organ benign neoplasm that is located in the cerebrovascular system

| [http://www.disease-ontology.org/?id=DOID:60007 DOID:60007]

|

|

|

|-

| cerebrovascular disease

| class of disease

| central nervous system disease
vascular disease
encephalopathy
central nervous system and retinal vascular disease
disease

| artery disease that is characterized by dysfunction of the blood vessels supplying the brain

| [http://www.disease-ontology.org/?id=DOID:6713 DOID:6713]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300 C10.228.140.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253 C14.907.253]

| Cerebrovascular diseases

| File:1471-2415-12-28-1Cerebral angiogram.jpg

|-

| cerebrum cancer

| class of disease

| supratentorial cancer
neoplasm of cerebral hemisphere

| supratentorial cancer that is located in the cerebrum

| [http://www.disease-ontology.org/?id=DOID:368 DOID:368]

|

|

|

|-

| ceruminoma

| class of disease

| apocrine sweat gland neoplasm
ceruminous tumor
apocrine adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7549 DOID:7549]

|

|

|

|-

| cervical Mullerian papilloma

| class of disease

| cervical benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9442 DOID:9442]

|

|

|

|-

| cervical Wilms' tumor

| class of disease

| cervical carcinosarcoma

| cervical carcinosarcoma is located in the cervix with morphological features resembling Wilms tumor of the kidney

| [http://www.disease-ontology.org/?id=DOID:5190 DOID:5190]

|

|

|

|-

| cervical adenocarcinoma

| class of disease

| cervix carcinoma
adenocarcinoma

| cervix carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:3702 DOID:3702]

|

| Adenocarcinoma of the cervix

|

|-

| cervical adenofibroma

| class of disease

| cervical benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5476 DOID:5476]

|

|

|

|-

| cervical adenoid basal carcinoma

| class of disease

| cervix carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6428 DOID:6428]

|

|

|

|-

| cervical adenoid cystic carcinoma

| class of disease

| cervix carcinoma
adenoid cystic carcinoma of the cervix uteri

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4867 DOID:4867]

|

|

|

|-

| cervical adenoma malignum

| class of disease

| cervical mucinous adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6627 DOID:6627]

|

|

|

|-

| cervical adenomyoma

| class of disease

| adenomyoma
cervical uterine cancer
cervical benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4995 DOID:4995]

|

|

|

|-

| cervical adenosarcoma

| class of disease

| cervical carcinosarcoma
malignant mixed epithelial and mesenchymal tumor of cervix uteri
adenosarcoma

| cervical carcinosarcoma that is located in the cervix

| [http://www.disease-ontology.org/?id=DOID:4111 DOID:4111]

|

|

|

|-

| cervical adenosquamous carcinoma

| class of disease

| adenosquamous carcinoma
cervical squamous cell carcinoma
squamous cell carcinoma
cervical uterine cancer

| cervical carcinoma that derives from squamous cells and gland-like cells

| [http://www.disease-ontology.org/?id=DOID:5636 DOID:5636]

|

|

|

|-

| cervical alveolar soft part sarcoma

| class of disease

| cervical uterine cancer

| alveolar soft part sarcoma and cervical soft tissue tumor and malignant neoplasm of cervix uteri that is located in the cervix

| [http://www.disease-ontology.org/?id=DOID:4442 DOID:4442]

|

|

|

|-

| cervical atypical polypoid adenomyoma

| class of disease

| cervical adenomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8179 DOID:8179]

|

|

|

|-

| cervical basaloid squamous cell carcinoma

| class of disease

| cervical squamous cell carcinoma
basaloid squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7046 DOID:7046]

|

|

|

|-

| cervical benign neoplasm

| class of disease

| uterine benign neoplasm
cervix disease
uterine cervix neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060110 DOID:0060110]

|

|

|

|-

| cervical carcinosarcoma

| class of disease

| cervical uterine cancer
malignant mixed epithelial and mesenchymal tumor of cervix uteri

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4112 DOID:4112]

|

|

|

|-

| cervical clear cell adenocarcinoma

| class of disease

| cervical adenocarcinoma
clear cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5303 DOID:5303]

|

|

|

|-

| cervical dystonia

| class of disease

| focal dystonia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050840 DOID:0050840]

|

|

|

|-

| cervical endometrial stromal sarcoma

| class of disease

| cervix endometrial stromal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4520 DOID:4520]

|

|

|

|-

| cervical endometrioid adenocarcinoma

| class of disease

| cervical adenocarcinoma
endometrial carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5830 DOID:5830]

|

|

|

|-

| cervical incompetence

| class of disease

| abnormality of organs and soft tissues of pelvis complicating pregnancy, childbirth, or the puerperium
cervix disease
disease

| cervix disease that is characterized by the beginning of dilation and effacement of a pregnant woman's cervix before her pregnancy has reached term

| [http://www.disease-ontology.org/?id=DOID:9681 DOID:9681]
[http://www.disease-ontology.org/?id=DOID:9678 DOID:9678]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.500.852.593.120 C12.050.351.500.852.593.120]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.703.039.089.339 C12.050.703.039.089.339]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.100.250.852.593.120 C12.100.250.852.593.120]

|

|

|-

| cervical keratinizing squamous cell carcinoma

| class of disease

| cervical squamous cell carcinoma
keratinizing squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7483 DOID:7483]

|

|

|

|-

| cervical large cell neuroendocrine carcinoma

| class of disease

| cervix carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6659 DOID:6659]

|

|

|

|-

| cervical lymphoepithelioma-like carcinoma

| class of disease

| cervical squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7598 DOID:7598]

|

|

|

|-

| cervical mucinous adenocarcinoma

| class of disease

| cervical adenocarcinoma
mucinous adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3701 DOID:3701]

|

|

|

|-

| cervical neuroblastoma

| class of disease

| extracranial neuroblastoma

| extracranial neuroblastoma that has material basis in immature nerve cells

| [http://www.disease-ontology.org/?id=DOID:0050935 DOID:0050935]

|

|

|

|-

| cervical non-keratinizing squamous cell carcinoma

| class of disease

| cervical squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7961 DOID:7961]

|

|

|

|-

| cervical polyp

| class of disease

| cervix disease
Uterine polyp

| cervix disease characterized by a benign polyp on the surface of the cervical canal

| [http://www.disease-ontology.org/?id=DOID:0060325 DOID:0060325]

|

| Cervical polyp

|

|-

| cervical serous adenocarcinoma

| class of disease

| cervical adenocarcinoma
serous cystadenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5752 DOID:5752]

|

|

|

|-

| cervical spinal canal and spinal cord meningioma

| class of disease

| spinal canal and spinal cord meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7915 DOID:7915]

|

|

|

|-

| cervical squamous cell carcinoma

| class of disease

| cervix carcinoma
squamous cell carcinoma

| cervix carcinoma that has material basis in squamous cells of the cervix

| [http://www.disease-ontology.org/?id=DOID:3744 DOID:3744]

|

|

|

|-

| cervical uterine cancer

| class of disease

| uterine cancer
cervix disease
uterine cervix neoplasm
disease

| cancer arising from the cervix

| [http://www.disease-ontology.org/?id=DOID:4362 DOID:4362]

|

| Cervical cancer

| File:Ca in situ, cervix 2.jpg

|-

| cervical verrucous carcinoma

| class of disease

| cervical squamous cell carcinoma
papillary carcinoma of the cervix uteri
verrucous carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3743 DOID:3743]

|

|

|

|-

| cervicitis

| class of disease

| cervix disease
disease

| inflammation of the uterine cervix

| [http://www.disease-ontology.org/?id=DOID:2568 DOID:2568]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.852.593.150 C13.351.500.852.593.150]

| Cervicitis

| File:Herpetic Cervicitis (8539801948).jpg

|-

| cervicomedullary junction neoplasm

| class of disease

| infratentorial cancer
Spinal cord cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4707 DOID:4707]

|

|

|

|-

| cervix carcinoma

| class of disease

| cervical uterine cancer
carcinoma

| cervical cancer that is located in the cervix uteri or located in the cervical area and that has material basis in abnormally proliferating cells derives from epithelial cells

| [http://www.disease-ontology.org/?id=DOID:2893 DOID:2893]

|

|

|

|-

| cervix disease

| class of disease

| uterine disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:2253 DOID:2253]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.852.593 C13.351.500.852.593]

| Diseases and disorders of cervix uteri

|

|-

| cervix endometrial stromal tumor

| class of disease

| cervical uterine cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4521 DOID:4521]

|

|

|

|-

| cervix endometriosis

| class of disease

| cervix disease
endometriosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:361 DOID:361]

|

|

|

|-

| cervix erosion

| class of disease

| cervix disease
disease

| ectropion

| [http://www.disease-ontology.org/?id=DOID:3456 DOID:3456]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.852.593.112 C13.351.500.852.593.112]

| Cervical ectropion

|

|-

| cervix melanoma

| class of disease

| cervical uterine cancer
mucosal melanoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4413 DOID:4413]

|

|

|

|-

| cervix small cell carcinoma

| class of disease

| cervix carcinoma
small cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6740 DOID:6740]

|

|

|

|-

| cervix squamous papilloma

| class of disease

| cervical benign neoplasm
papilloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9445 DOID:9445]

|

|

|

|-

| cervix uteri carcinoma in situ

| class of disease

| cervical intraepithelial neoplasia
cervix disease
uterus carcinoma in situ

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8991 DOID:8991]

|

|

|

|-

| cheilitis

| class of disease

| lip disease
inflammation

| inflammation of the lips

| [http://www.disease-ontology.org/?id=DOID:1762 DOID:1762]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.409.215 C07.465.409.215]

| Cheilitis

|

|-

| chemical colitis

| class of disease

| colitis

| colitis caused by introduction of various chemicals

| [http://www.disease-ontology.org/?id=DOID:0060186 DOID:0060186]

|

|

|

|-

| cherry allergy

| class of disease

| fruit allergy

| fruit allergy triggered by Prunus avium plant fruit food product.

| [http://www.disease-ontology.org/?id=DOID:0060506 DOID:0060506]

|

|

|

|-

| chest wall bone cancer

| class of disease

| bone cancer
chest wall lymphoma

| bone cancer and malignant neoplasm of chest wall that is located in the chest wall

| [http://www.disease-ontology.org/?id=DOID:6579 DOID:6579]

|

|

|

|-

| chest wall lymphoma

| class of disease

| malignant neoplasm of chest wall
thoracic cancer
lymphoma

| thoracic cancer that is located in the chest wall

| [http://www.disease-ontology.org/?id=DOID:6758 DOID:6758]

|

|

|

|-

| chest wall parachordoma

| class of disease

| parachordoma
chest wall lymphoma
neoplasm of chest wall
mesenchymal cell neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8043 DOID:8043]

|

|

|

|-

| chiasmal syndrome

| class of disease

| optic nerve disease
encephalopathy

| optic nerve disease that is characterized by lesions of the optic chiasm, manifesting as various impairments of the sufferer's visual field according to the location of the lesion along the optic nerve

| [http://www.disease-ontology.org/?id=DOID:5655 DOID:5655]

|

|

|

|-

| chicken egg allergy

| class of disease

| egg allergy

| egg allergy triggered by Gallus gallus eggs

| [http://www.disease-ontology.org/?id=DOID:0060492 DOID:0060492]

|

|

|

|-

| chief cell adenoma

| class of disease

| parathyroid adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7607 DOID:7607]

|

|

|

|-

| childhood absence epilepsy

| class of disease
symptom or sign

| absence seizure
childhood electroclinical syndrome
Idiopathic generalized epilepsy
generalized seizure

| childhood electroclinical syndrome characterized by the occurrence of typical absence seizures, starting between the age of four and ten years

| [http://www.disease-ontology.org/?id=DOID:1825 DOID:1825]

|

|

|

|-

| childhood acute lymphocytic leukemia

| class of disease

| acute lymphocytic leukemia
childhood leukemia

| acute lymphocytic leukemia occuring during childhood

| [http://www.disease-ontology.org/?id=DOID:0080144 DOID:0080144]

|

|

|

|-

| childhood acute megakaryoblastic leukemia

| class of disease

| acute megakaryoblastic leukemia

| disease

| [http://www.disease-ontology.org/?id=DOID:0080794 DOID:0080794]

|

|

|

|-

| childhood acute myeloid leukemia

| class of disease

| childhood leukemia
bilineal acute myeloid leukemia
acute myeloid leukemia

| Acute myeloid leukemia occurring in childhood

| [http://www.disease-ontology.org/?id=DOID:0070323 DOID:0070323]

|

|

|

|-

| childhood asthma

| class of disease

| asthma
chronic asthma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080815 DOID:0080815]

|

|

|

|-

| childhood botryoid rhabdomyosarcoma

| class of disease

| botryoid embryo rhabdomyosarcoma
Childhood Rhabdomyosarcoma
rare childhood malignant neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6786 DOID:6786]

|

|

|

|-

| childhood brain germinoma

| class of disease

| brain germinoma
childhood central nervous system germinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7429 DOID:7429]

|

|

|

|-

| childhood brain meningioma

| class of disease

| brain meningioma
rare childhood malignant neoplasm
pediatric meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6939 DOID:6939]

|

|

|

|-

| childhood brain stem glioma

| class of disease

| childhood brain stem neoplasm
Brainstem glioma
rare childhood malignant neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6383 DOID:6383]

|

|

|

|-

| childhood brain stem neoplasm

| class of disease

| brain stem neoplasm
childhood cancer
childhood infratentorial neoplasm
brain stem cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4206 DOID:4206]

|

|

|

|-

| childhood brainstem astrocytoma

| class of disease

| childhood brain stem glioma
brain stem astrocytic neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:6386 DOID:6386]

|

|

|

|-

| childhood central nervous system germinoma

| class of disease

| central nervous system germinoma
malignant childhood germ cell neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8078 DOID:8078]

|

|

|

|-

| childhood central nervous system immature teratoma

| class of disease

| central nervous system immature teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6654 DOID:6654]

|

|

|

|-

| childhood central nervous system mature teratoma

| class of disease

| central nervous system mature teratoma
pediatric central nervous system tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6423 DOID:6423]

|

|

|

|-

| childhood central nervous system mixed germ cell tumor

| class of disease

| central nervous system childhood germ cell tumor
malignant childhood germ cell neoplasm
mixed germ cell tumor of central nervous system
rare childhood malignant neoplasm
brain cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7516 DOID:7516]

|

|

|

|-

| childhood central nervous system primitive neuroectodermal neoplasm

| class of disease

| central nervous system primitive neuroectodermal neoplasm
childhood cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3870 DOID:3870]

|

|

|

|-

| childhood cerebellar astrocytic neoplasm

| class of disease

| cerebellar astrocytoma
childhood cerebellar neoplasm
juvenile astrocytoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6286 DOID:6286]

|

|

|

|-

| childhood cerebellar neoplasm

| class of disease

| cerebellum cancer
childhood infratentorial neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5059 DOID:5059]

|

|

|

|-

| childhood cerebral astrocytoma

| class of disease

| cerebrum cancer
juvenile astrocytoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7007 DOID:7007]

|

|

|

|-

| childhood choriocarcinoma of the ovary

| class of disease

| choriocarcinoma of ovary
rare childhood malignant neoplasm
non-gestational ovarian choriocarcinoma
malignant childhood germ cell neoplasm
pediatric ovarian germ cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8336 DOID:8336]

|

|

|

|-

| childhood choriocarcinoma of the testis

| class of disease

| choriocarcinoma of the testis
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm
pediatric testicular germ cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6160 DOID:6160]

|

|

|

|-

| childhood choroid plexus cancer

| class of disease

| childhood cancer
childhood choroid plexus neoplasm
choroid plexus neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3545 DOID:3545]

|

|

|

|-

| childhood disintegrative disease

| class of disease

| pervasive developmental disorder
disease

| neurodevelopmental condition

| [http://www.disease-ontology.org/?id=DOID:13487 DOID:13487]

|

|

|

|-

| childhood electroclinical syndrome

| class of disease

| electroclinical syndrome
Epilepsy in children
absence seizure

| electroclinical syndrome with onset in childhood between one and 12 years of age

| [http://www.disease-ontology.org/?id=DOID:0050704 DOID:0050704]

|

|

|

|-

| childhood embryonal testis carcinoma

| class of disease

| embryonal testis carcinoma
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm
pediatric testicular germ cell tumor

| embryonal testis carcinoma that occurs in children

| [http://www.disease-ontology.org/?id=DOID:6162 DOID:6162]

|

|

|

|-

| childhood endodermal sinus tumor

| class of disease

| endodermal sinus tumor
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm

| endodermal sinus tumor that occurs in children

| [http://www.disease-ontology.org/?id=DOID:5342 DOID:5342]

|

|

|

|-

| childhood extraosseous osteosarcoma

| class of disease

| extraosseous osteosarcoma
pediatric osteosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7297 DOID:7297]

|

|

|

|-

| childhood germ cell brain tumor

| class of disease

| central nervous system childhood germ cell tumor
brain cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7430 DOID:7430]

|

|

|

|-

| childhood hypophosphatasia

| class of disease

| hypophosphatasia

| A hypophosphatasia that has material basis in an autosomal recessive mutation of ALPL on chromosome 1p36.12.

| [http://www.disease-ontology.org/?id=DOID:0110915 DOID:0110915]

|

|

|

|-

| childhood immature teratoma of ovary

| class of disease

| immature teratoma of ovary
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm
childhood teratoma of the ovary

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7037 DOID:7037]

|

|

|

|-

| childhood infratentorial neoplasm

| class of disease

| brain stem cancer
infratentorial cancer
childhood neoplasm
childhood brain tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4207 DOID:4207]

|

|

|

|-

| childhood intracortical osteosarcoma

| class of disease

| pediatric osteosarcoma
intracortical osteogenic sarcoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:7612 DOID:7612]

|

|

|

|-

| childhood kidney angiomyolipoma

| class of disease

| childhood kidney neoplasm
kidney angiomyolipoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8410 DOID:8410]

|

|

|

|-

| childhood kidney cell carcinoma

| class of disease

| renal cell carcinoma
rare childhood malignant neoplasm
childhood malignant kidney neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4454 DOID:4454]

|

|

|

|-

| childhood kidney neoplasm

| class of disease

| kidney neoplasm
childhood neoplasm
kidney cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3675 DOID:3675]

|

|

|

|-

| childhood leukemia

| class of disease

| leukemia
childhood cancer
rare childhood malignant neoplasm
bone marrow cancer

| leukemia that occurs in children

| [http://www.disease-ontology.org/?id=DOID:7757 DOID:7757]

|

|

|

|-

| childhood malignant hemangiopericytoma

| class of disease

| hemangiopericytoma
hemangiopericytoma, malignant

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7731 DOID:7731]

|

|

|

|-

| childhood malignant mesenchymoma

| class of disease

| malignant mesenchymoma
childhood cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5893 DOID:5893]

|

|

|

|-

| childhood malignant schwannoma

| class of disease

| malignant peripheral nerve sheath tumor
neurilemmoma
rare childhood malignant neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7732 DOID:7732]

|

|

|

|-

| childhood mature teratoma of the ovary

| class of disease

| childhood teratoma of the ovary
mature teratoma of the ovary

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6229 DOID:6229]

|

|

|

|-

| childhood mediastinal neurogenic tumor

| class of disease

| malignant mediastinal neurogenic neoplasm
childhood neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4690 DOID:4690]

|

|

|

|-

| childhood medulloblastoma

| class of disease

| medulloblastoma
childhood infratentorial neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3869 DOID:3869]

|

|

|

|-

| childhood multilocular cystic kidney neoplasm

| class of disease

| kidney benign neoplasm
childhood kidney neoplasm
multiloculated renal cyst

| A childhood renal Wilms cancer that occurs in children. It encompasses two histologically distinct but grossly indistinguishable lesions: cystic nephroma and cystic partially differentiated nephroblastoma (CPDN).

| [http://www.disease-ontology.org/?id=DOID:7762 DOID:7762]

|

|

|

|-

| childhood oligodendroglioma

| class of disease

| oligodendroglioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3183 DOID:3183]

|

|

|

|-

| childhood onset epileptic encephalopathy

| class of disease

| generalized epilepsy
Epilepsy in children

| An idiopathic generalized epilepsy characterized by onset of multiple seizure types in the first few years of life and associated with poor prognosis. Affected individuals have cognitive regression and intellectual disability.

| [http://www.disease-ontology.org/?id=DOID:0060475 DOID:0060475]

|

|

|

|-

| childhood optic nerve glioma

| class of disease

| optic nerve glioma

| human disease

| [http://www.disease-ontology.org/?id=DOID:6576 DOID:6576]

|

|

|

|-

| childhood ovarian embryonal carcinoma

| class of disease

| ovarian embryonal carcinoma
pediatric ovarian germ cell tumor
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm

| ovarian embryonal carcinoma that occurs in childhood

| [http://www.disease-ontology.org/?id=DOID:8036 DOID:8036]

|

|

|

|-

| childhood ovarian endodermal sinus tumor

| class of disease

| ovarian endodermal sinus tumor
pediatric ovarian germ cell tumor
childhood endodermal sinus tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6083 DOID:6083]

|

|

|

|-

| childhood parosteal osteogenic sarcoma

| class of disease

| juxtacortical osteosarcoma
pediatric osteosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5809 DOID:5809]

|

|

|

|-

| childhood pilocytic astrocytoma

| class of disease

| pilocytic astrocytoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6812 DOID:6812]

|

|

|

|-

| childhood pleomorphic rhabdomyosarcoma

| class of disease

| pleomorphic rhabdomyosarcoma
Childhood Rhabdomyosarcoma
rare childhood malignant neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7463 DOID:7463]

|

|

|

|-

| childhood spinal cord tumor

| class of disease

| Spinal cord cancer
childhood cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3637 DOID:3637]

|

|

|

|-

| childhood teratocarcinoma of the testis

| class of disease

| childhood testicular mixed germ cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6474 DOID:6474]

|

|

|

|-

| childhood teratoma of the ovary

| class of disease

| ovarian germ cell teratoma
pediatric ovarian germ cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6230 DOID:6230]

|

|

|

|-

| childhood testicular mixed germ cell tumor

| class of disease

| mixed testicular germ cell tumor
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm
pediatric testicular germ cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6161 DOID:6161]

|

|

|

|-

| childhood type dermatomyositis

| class of disease

| dermatomyositis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14203 DOID:14203]

|

|

|

|-

| childhood vagina botryoid rhabdomyosarcoma

| class of disease

| vagina botryoid rhabdomyosarcoma
childhood botryoid rhabdomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6787 DOID:6787]

|

|

|

|-

| chloramine T respiratory allergy

| class of disease

| metal allergy
respiratory allergy

| respiratory allergy that has allergic trigger chloramine T

| [http://www.disease-ontology.org/?id=DOID:0040062 DOID:0040062]

|

|

|

|-

| chlorhexidine allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger chlorhexidine

| [http://www.disease-ontology.org/?id=DOID:0040026 DOID:0040026]

|

|

|

|-

| cholangiocarcinoma

| class of disease

| bile duct adenocarcinoma
disease

| bile duct adenocarcinoma that has material basis in bile duct epithelial cells.

| [http://www.disease-ontology.org/?id=DOID:4947 DOID:4947]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.450 C04.557.470.200.025.450]

| Cholangiocarcinoma

| File:ERCP cholangioca.jpg

|-

| cholangiolocellular carcinoma

| class of disease

| intrahepatic cholangiocarcinoma
rare parenchymal liver disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7642 DOID:7642]

|

|

|

|-

| cholecystitis

| class of disease
symptom or sign

| ascending cholangitis
disease

| cholangitis that is characterized by an inflammation that is located in the gallbladder

| [http://www.disease-ontology.org/?id=DOID:1949 DOID:1949]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.564.263 C06.130.564.263]

| Cholecystitis

|

|-

| cholecystolithiasis

| class of disease

| gallbladder disease
gallstone

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11151 DOID:11151]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.409.178 C06.130.409.178]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.564.332 C06.130.564.332]

|

|

|-

| choledochal cyst

| class of disease

| bile duct disease
disease

| congenital disorder of digestive system

| [http://www.disease-ontology.org/?id=DOID:899 DOID:899]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.182.198 C04.182.198]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.120.127 C06.130.120.127]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.198.184 C06.198.184]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.314.184 C16.131.314.184]

| Choledochal cysts

|

|-

| choledocholithiasis

| class of disease

| gallbladder disease
common bile duct disease
endocrine system disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11755 DOID:11755]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.120.250.174 C06.130.120.250.174]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.409.267 C06.130.409.267]

| Choledocholithiasis

| File:MRCP Choledocholithiasis.jpg

|-

| cholelithiasis

| class of disease

| gallbladder disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10211 DOID:10211]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.409 C06.130.409]

| Cholelithiasis

| File:Gallstones.jpg

|-

| cholestasis

| class of disease

| bile duct disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13580 DOID:13580]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.120.135 C06.130.120.135]

| Cholestasis

| File:Bilirubin pigment in cholestatic liver 40X.jpg

|-

| cholesteatoma

| class of disease

| keratosis
disease

| keratosis characterized by keratinizing squamous epithelium located in middle ear and/or mastoid, subepithelial connective tissue and by the progressive accumulation of keratin debris with or without surrounding inflammatory reaction

| [http://www.disease-ontology.org/?id=DOID:869 DOID:869]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.428.260 C17.800.428.260]

| Cholesteatoma

| File:Cholesteatom kuppelraum 1a.jpg

|-

| cholesterol embolism

| class of disease

| vascular disease
embolism

| vascular disease with blood vessel obstruction resulting from the release of cholesterol

| [http://www.disease-ontology.org/?id=DOID:1461 DOID:1461]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.355.350.454.500 C14.907.355.350.454.500]

| Cholesterol embolism

|

|-

| choline deficiency disease

| class of disease

| nutritional deficiency disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8456 DOID:8456]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.654.521.500.133.699.160 C18.654.521.500.133.699.160]

|

|

|-

| cholinergic urticaria

| class of disease

| physical urticaria
disease

| urticaria induced by sweating

| [http://www.disease-ontology.org/?id=DOID:14443 DOID:14443]

|

|

|

|-

| chondroblastic osteosarcoma

| class of disease

| osteosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3372 DOID:3372]

|

|

|

|-

| chondroblastoma

| class of disease

| connective tissue neoplasm
connective tissue benign neoplasm
benign neoplasms by histologic type
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2649 DOID:2649]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.250 C04.557.450.565.250]

| Chondroblastoma

| File:Chondroblastoma - very high mag.jpg

|-

| chondrodysplasia with joint dislocations gPAPP type

| class of disease

| autosomal recessive disease
osteochondrodysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112224 DOID:0112224]

|

|

|

|-

| chondroid chordoma

| class of disease

| chordoma

| chordoma that histologically derives from chordoma, derives from chondroma, and derives from chondrosarcoma

| [http://www.disease-ontology.org/?id=DOID:4152 DOID:4152]

|

|

|

|-

| chondroid lipoma

| class of disease

| lipoma

| lipoma that is a deep-seated, firm, yellow tumors that characteristically occur on the legs of women

| [http://www.disease-ontology.org/?id=DOID:10208 DOID:10208]

|

|

|

|-

| chondroid syringoma of the vulva

| class of disease

| eccrine mixed tumor of skin
vulvar benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2078 DOID:2078]

|

|

|

|-

| chondroma

| class of disease

| benign neoplasms by histologic type
cartilage tumor
disease

| cell type benign neoplasm that is a cartilaginous tumor encapsulated with a lobular growing pattern

| [http://www.disease-ontology.org/?id=DOID:2602 DOID:2602]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.265 C04.557.450.565.265]

| Chondroma

|

|-

| chondromalacia

| class of disease

| articular cartilage disease

|

| [http://www.disease-ontology.org/?id=DOID:2557 DOID:2557]

|

|

|

|-

| chondropathy

| class of disease

| osteochondropathy
connective tissue disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1222 DOID:1222]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.182 C05.182]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.182 C17.300.182]

| Chondropathies

|

|-

| chordoid meningioma

| class of disease

| clear cell meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8368 DOID:8368]

|

|

|

|-

| chordoma

| class of disease

| notochordal cancer
disease

| notochordal cancer that derives from cellular remnants of the notochord

| [http://www.disease-ontology.org/?id=DOID:3302 DOID:3302]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.220 C04.557.465.220]

| Chordoma

| File:Chordoma.JPG

|-

| chorea gravidarum

| class of disease

| choreatic disease
complications of pregnancy
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14483 DOID:14483]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.079.294 C10.228.140.079.294]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.662.262.249.500 C10.228.662.262.249.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.141 C13.703.141]

|

|

|-

| chorioamnionitis

| class of disease

| placenta disease
disease

| placenta disease that is an inflammation of the fetal membranes (amnion and chorion) due to a bacterial infection

| [http://www.disease-ontology.org/?id=DOID:0050697 DOID:0050697]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.277.030 C13.703.277.030]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.420.339.260 C13.703.420.339.260]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.590.268 C13.703.590.268]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.300.030 C16.300.030]

| Chorioamnionitis

| File:Chorioamnionitis - high mag.jpg

|-

| chorioangioma

| class of disease

| placenta disease
uterine benign neoplasm
hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:277 DOID:277]

|

| Chorangioma

| File:Chorangioma - low mag.jpg

|-

| choriocarcinoma

| class of disease

| placenta cancer
trophoblastic neoplasm
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3594 DOID:3594]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.955.207 C04.557.465.955.207]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.455 C04.557.470.200.025.455]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.850.908.208 C04.850.908.208]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.720.949.208 C13.703.720.949.208]

| Choriocarcinoma

| File:Metastatic choriocarcinoma Case 140 (4858357750).jpg

|-

| choriocarcinoma of ovary

| class of disease

| malignant ovarian germ cell neoplasm
non-gestational choriocarcinoma
choriocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5550 DOID:5550]

|

|

|

|-

| choriocarcinoma of the testis

| class of disease

| non-gestational choriocarcinoma
testicular non-seminomatous germ cell cancer
choriocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5551 DOID:5551]

|

|

|

|-

| chorioretinal scar

| class of disease

| retinal disease
scar

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11086 DOID:11086]

|

|

|

|-

| chorioretinitis

| class of disease
symptom or sign

| eye disease
uveitis
disease

| inflammation of the choroid

| [http://www.disease-ontology.org/?id=DOID:8886 DOID:8886]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.768.773.348 C11.768.773.348]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.160.478.400 C11.941.160.478.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.879.780.900.300.318 C11.941.879.780.900.300.318]

| Chorioretinitis

| File:Chorioretinitis AIDS nci-vol-2169-300.jpg

|-

| choroid cancer

| class of disease

| uveal cancer
choroid neoplasm
choroid disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12759 DOID:12759]

|

|

|

|-

| choroid disease

| class of disease

| uveal disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1417 DOID:1417]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.160 C11.941.160]

|

|

|-

| choroid plexus carcinoma

| class of disease

| choroid plexus neoplasm
carcinoma

| choroid plexus cancer that has material basis in epithelial cells of the choroid plexus

| [http://www.disease-ontology.org/?id=DOID:5648 DOID:5648]

|

| Choroid plexus carcinoma

| File:Choroidplexuscarcinoma.png

|-

| choroid plexus meningioma

| class of disease

| choroid plexus neoplasm
meningioma
cerebral meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4584 DOID:4584]

|

|

|

|-

| choroid plexus neoplasm

| class of disease

| cerebral ventricle neoplasm
cerebral ventricle cancer

| cerebral ventricle neoplasm that is located in the plexus located in the ventricles of the brain

| [http://www.disease-ontology.org/?id=DOID:3540 DOID:3540]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.614.250.195.205.200 C04.588.614.250.195.205.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.211.280.300 C10.228.140.211.280.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.551.240.250.200.200 C10.551.240.250.200.200]

| Choroid plexus cancers

|

|-

| choroid plexus papilloma

| class of disease

| papilloma
choroid plexus neoplasm
cerebrovascular benign neoplasm

| Benign brain tumor

| [http://www.disease-ontology.org/?id=DOID:2626 DOID:2626]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.614.250.195.205.200.500 C04.588.614.250.195.205.200.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.211.280.300.500 C10.228.140.211.280.300.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.551.240.250.200.200.500 C10.551.240.250.200.200.500]

| Choroid plexus papilloma

| File:Plexuspapillom Makroskopie.png

|-

| choroidal sclerosis

| class of disease

| eye degenerative disease
choroid disease

| neurodegenerative disease that involves the optic choroid

| [http://www.disease-ontology.org/?id=DOID:980 DOID:980]

|

|

|

|-

| choroiditis

| class of disease

| choroid disease
uveitis

| inflammation of the choroid

| [http://www.disease-ontology.org/?id=DOID:11406 DOID:11406]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.160.478 C11.941.160.478]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.879.780.900.300 C11.941.879.780.900.300]

|

|

|-

| chromium allergic contact dermatitis

| class of disease

| allergic contact dermatitis
metal allergy

| allergic contact dermatitis that has allergic trigger chromium atom

| [http://www.disease-ontology.org/?id=DOID:0040056 DOID:0040056]

|

|

|

|-

| chromophobe renal cell carcinoma

| class of disease

| renal cell carcinoma

| renal cell carcinoma that has material basis in chromophobe cell that appear pale when viewed under microscope, but that are larger and display different features than clear cells

| [http://www.disease-ontology.org/?id=DOID:4471 DOID:4471]

|

| Chromophobe renal cell carcinoma

|

|-

| chromosomal deletion syndrome

| class of disease

| chromosomal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060388 DOID:0060388]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.210.050.500.500 C23.550.210.050.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=G05.365.590.029.530.175 G05.365.590.029.530.175]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=G05.365.590.175.050.500.500 G05.365.590.175.050.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=G05.365.590.762.180 G05.365.590.762.180]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=G05.558.800.180 G05.558.800.180]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=G05.700.131.500.500 G05.700.131.500.500]

| Chromosome deletion

|

|-

| chromosomal duplication syndrome

| class of disease

| chromosomal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060429 DOID:0060429]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.210.182 C23.550.210.182]

|

|

|-

| chromosome 10q23 deletion syndrome

| class of disease

| chromosomal deletion syndrome
partial monosomy of the long arm of chromosome 10

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060389 DOID:0060389]

|

|

|

|-

| chromosome 13q14 deletion syndrome

| class of disease

| chromosomal deletion syndrome
autosomal dominant disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060391 DOID:0060391]

|

|

|

|-

| chromosome 17p13.1 deletion syndrome

| class of disease

| chromosomal deletion syndrome
classical lissencephalies and subcortical band heterotopias
autosomal dominant disease
partial monosomy of the short arm of chromosome 17

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060402 DOID:0060402]

|

|

|

|-

| chromosome 18p deletion syndrome

| class of disease

| chromosomal deletion syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060406 DOID:0060406]

|

|

|

|-

| chromosome 18q deletion syndrome

| class of disease

| chromosomal deletion syndrome
partial deletion of the long arm of chromosome 18
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060407 DOID:0060407]

|

| Distal 18q-

|

|-

| chromosome 19p13.13 deletion syndrome

| class of disease

| chromosomal deletion syndrome
autosomal dominant disease
partial deletion of the short arm of chromosome 19

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060426 DOID:0060426]

|

|

|

|-

| chromosome 1q41-q42 deletion syndrome

| class of disease

| chromosomal deletion syndrome

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060412 DOID:0060412]

|

|

|

|-

| chromosome 3-linked frontotemporal dementia

| class of disease

| frontotemporal dementia

| A frontotemporal dementia that has material basis in heterozygous mutation in CHMP2B on 3p11.2.

| [http://www.disease-ontology.org/?id=DOID:0111227 DOID:0111227]

|

|

|

|-

| chromosome Xp11.22 duplication syndrome

| class of disease

| partial duplication of the short arm of chromosome X
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112037 DOID:0112037]

|

|

|

|-

| chronic NK-cell lymphocytosis

| class of disease

| type IV hypersensitivity
mature T-cell neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7465 DOID:7465]

|

|

|

|-

| chronic apical periodontitis

| class of disease

| periapical periodontitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11269 DOID:11269]

|

|

|

|-

| chronic asthma

| class of disease

| asthma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080809 DOID:0080809]

|

|

|

|-

| chronic atticoantral disease

| class of disease

| chronic purulent otitis media

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14248 DOID:14248]

|

|

|

|-

| chronic cervicitis

| class of disease

| cervicitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1513 DOID:1513]

|

|

|

|-

| chronic cholangitis

| class of disease

| ascending cholangitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9439 DOID:9439]

|

|

|

|-

| chronic closed-angle glaucoma

| class of disease

| primary angle-closure glaucoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14445 DOID:14445]

|

|

|

|-

| chronic conjunctivitis

| class of disease

| conjunctivitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2475 DOID:2475]

|

|

|

|-

| chronic cystitis

| class of disease

| cystitis
chronic condition

| Recurrent infections of the urinary bladder

| [http://www.disease-ontology.org/?id=DOID:1680 DOID:1680]

|

| Chronic cystitis

|

|-

| chronic dacryoadenitis

| class of disease

| dacryoadenitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:949 DOID:949]

|

|

|

|-

| chronic dacryocystitis

| class of disease

| chronic inflammation of lacrimal passage
dacryocystitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9937 DOID:9937]

|

|

|

|-

| chronic duodenal ileus

| class of disease

| duodenal obstruction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13687 DOID:13687]

|

|

|

|-

| chronic eosinophilic leukemia

| class of disease

| chronic leukemia
eosinophilic leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080367 DOID:0080367]

|

|

|

|-

| chronic ethmoiditis

| class of disease

| ethmoid sinusitis
chronic rhinosinusitis

| ethmoid sinusitis which lasts for 12 weeks or more

| [http://www.disease-ontology.org/?id=DOID:9312 DOID:9312]

|

|

|

|-

| chronic eustachian salpingitis

| class of disease

| otosalpingitis

| otosalpingitis which is persistent and long-lasting

| [http://www.disease-ontology.org/?id=DOID:1999 DOID:1999]

|

|

|

|-

| chronic fatigue syndrome

| class of disease
symptom or sign

| syndrome
primary immunodeficiency disease
disease

| medical condition involving extreme fatigue and a wide range of other symptoms

| [http://www.disease-ontology.org/?id=DOID:8544 DOID:8544]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C02.330 C02.330]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.310 C05.651.310]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.440.600 C10.228.440.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.364 C10.668.364]

|

| File:Statistical parametric maps of BPND of 11C-(R)-PK11195 in CFS.ME patients and healthy controls.gif

|-

| chronic follicular conjunctivitis

| class of disease

| chronic conjunctivitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13326 DOID:13326]

|

|

|

|-

| chronic frontal sinusitis

| class of disease

| frontal sinusitis
chronic condition

| frontal sinusitis which lasts for 12 weeks or more. This causes steady headache, localized tenderness and intermittent, purulent nasal and postnasal drainage.

| [http://www.disease-ontology.org/?id=DOID:10790 DOID:10790]

|

|

|

|-

| chronic fungal otitis externa

| class of disease

| otomycosis
fungal infectious disease

| otomycosis which is persistent and long-lasting or recurrent

| [http://www.disease-ontology.org/?id=DOID:10519 DOID:10519]

|

|

|

|-

| chronic gastritis

| class of disease

| gastritis
stomach disease

| Inflammation of the stomach that is chronic in nature

| [http://www.disease-ontology.org/?id=DOID:4029 DOID:4029]

|

|

|

|-

| chronic gonococcal salpingitis

| class of disease

| chronic salpingitis
gonococcal infectious diseases

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12718 DOID:12718]

|

|

|

|-

| chronic gonorrhea of cervix

| class of disease

| chronic cervicitis
gonococcal infectious diseases

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1512 DOID:1512]

|

|

|

|-

| chronic inducible urticaria

| class of disease

| chronic urticaria

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080748 DOID:0080748]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.862.945.533.500 C17.800.862.945.533.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.904.533.500 C20.543.480.904.533.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.291.500.360.500 C23.550.291.500.360.500]

|

|

|-

| chronic inflammation of lacrimal passage

| class of disease

| chronic inflammatory response
lacrimal apparatus disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9935 DOID:9935]

|

|

|

|-

| chronic inflammatory demyelinating polyneuritis

| class of disease

| inflammatory and toxic neuropathy
chronic inflammatory demyelinating polyradiculoneuropathy
demyelinating polyneuropathy

| An immunologic inflammatory disorder characterized by loss of myelin in the peripheral nerves. Patients present with progressive weakness and loss of sensory function in the legs and arms.

| [http://www.disease-ontology.org/?id=DOID:2536 DOID:2536]

|

|

|

|-

| chronic interstitial cystitis

| class of disease

| interstitial cystitis
chronic cystitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:1678 DOID:1678]

|

|

|

|-

| chronic intestinal vascular insufficiency

| class of disease

| intestinal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8633 DOID:8633]

|

|

|

|-

| chronic lacrimal gland enlargement

| class of disease

| dacryoadenitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12809 DOID:12809]

|

|

|

|-

| chronic laryngitis

| class of disease

| laryngitis

| A laryngitis in which symptoms last longer than three weeks. Gastroesophageal reflux, and lingering bronchitis can cause the disease.

| [http://www.disease-ontology.org/?id=DOID:11797 DOID:11797]

|

|

|

|-

| chronic leukemia

| class of disease

| leukemia

| broad type of leukemia; disjoint with acute leukemia

| [http://www.disease-ontology.org/?id=DOID:1036 DOID:1036]

|

| Chronic leukemias

|

|-

| chronic lymphocytic leukemia

| class of disease
symptom or sign

| lymphoblastic leukemia
chronic leukemia
small lymphocytic lymphoma
lymphoma
leukemia
disease

| lymphoblastic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood

| [http://www.disease-ontology.org/?id=DOID:1040 DOID:1040]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.428.080.125 C04.557.337.428.080.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.560.080.125 C15.604.515.560.080.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.528.080.125 C20.683.515.528.080.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.508.428.080.125 C15.378.508.428.080.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.291.500.483 C23.550.291.500.483]

| Chronic lymphocytic leukemia

| File:Chronic lymphocytic leukemia.jpg

|-

| chronic lymphocytic leukemia and small lymphocytic lymphoma

| class of disease

| chronic lymphocytic leukemia

| chronic lymphocytic leukemia that is characterized by the presence of immature lymphocytes in the blood and bone marrow and/or in the lymph nodes

| [http://www.disease-ontology.org/?id=DOID:6354 DOID:6354]

|

|

|

|-

| chronic maxillary sinusitis

| class of disease

| maxillary sinusitis
chronic condition

| maxillary sinusitis which lasts for 12 weeks or more

| [http://www.disease-ontology.org/?id=DOID:10792 DOID:10792]

|

|

|

|-

| chronic meningitis

| class of disease

| meningitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10341 DOID:10341]

|

|

|

|-

| chronic metabolic polyneuropathy

| class of disease

| chronic polyneuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7441 DOID:7441]

|

|

|

|-

| chronic monocytic leukemia

| class of disease

| monocytic leukemia
chronic myelomonocytic leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:8593 DOID:8593]

|

|

|

|-

| chronic myeloid leukemia

| class of disease

| myeloid leukemia
chronic leukemia
disease

| myeloid leukemia that is characterized by over production of white blood cells

| [http://www.disease-ontology.org/?id=DOID:8552 DOID:8552]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.539.250 C04.557.337.539.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.190.636.370 C15.378.190.636.370]

| Chronic myeloid leukemia

| File:Bcrablmet.jpg

|-

| chronic myelomonocytic leukemia

| class of disease

| monocytic leukemia
chronic myeloid leukemia
chronic leukemia

| chronic leukemia characterized by monocytosis, increased monocytes in the bone marrow, variable degrees of dysplasia, but an absence of immature granulocytes in the blood

| [http://www.disease-ontology.org/?id=DOID:0080188 DOID:0080188]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.539.522 C04.557.337.539.522]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.190.615.510 C15.378.190.615.510]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.508.539.522 C15.378.508.539.522]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.291.500.495 C23.550.291.500.495]

| Chronic myelomonocytic leukemia

|

|-

| chronic neutrophilic leukemia

| class of disease

| myeloproliferative disorders
chronic leukemia

| chronic leukemia characterized by neutrophilic leukocytosis with no detectable Philadelphia chromosome or BCR/ABL fusion gene

| [http://www.disease-ontology.org/?id=DOID:0080187 DOID:0080187]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.190.636.380 C15.378.190.636.380]

|

|

|-

| chronic obstructive pulmonary disease

| class of disease

| obstructive lung disease
disease

| lung disease involving long-term poor airflow

| [http://www.disease-ontology.org/?id=DOID:3083 DOID:3083]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.495.389 C08.381.495.389]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.291.500.875 C23.550.291.500.875]

| Chronic obstructive pulmonary disease

| File:Centrilobular emphysema 865 lores.jpg

|-

| chronic orbital inflammation

| class of disease

| orbital disease
chronic inflammatory response

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1397 DOID:1397]

|

|

|

|-

| chronic perichondritis of pinna

| class of disease

| perichondritis of auricle
pinna disease

| perichondritis of auricle which is persistent and long-lasting

| [http://www.disease-ontology.org/?id=DOID:14243 DOID:14243]

|

|

|

|-

| chronic polyneuropathy

| class of disease

| polyneuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5221 DOID:5221]

|

|

|

|-

| chronic pulmonary eosinophilia

| class of disease

| eosinophilic pneumonia

| An eosinophilic pneumonia which slowly progresses over weeks to months. Life-threatening shortness of breath can develop if the condition is not treated. Individuals are often diagnosed with asthma before the advent of this disease.

| [http://www.disease-ontology.org/?id=DOID:9502 DOID:9502]

|

|

|

|-

| chronic pulmonary heart disease

| class of disease

| cor pulmonale

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12326 DOID:12326]

|

|

|

|-

| chronic purulent otitis media

| class of disease

| suppurative otitis media
chronic otitis media

| suppurative otitis media which is persistent and long-lasting

| [http://www.disease-ontology.org/?id=DOID:14247 DOID:14247]

|

|

|

|-

| chronic pyelonephritis

| class of disease

| pyelonephritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1076 DOID:1076]

|

| Chronic pyelonephritis

|

|-

| chronic rapidly progressive glomerulonephritis

| class of disease

| glomerulonephritis
rapidly progressive glomerulonephritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11036 DOID:11036]

|

|

|

|-

| chronic rheumatic pericarditis

| class of disease

| pericarditis
rheumatic heart disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1869 DOID:1869]
[http://www.disease-ontology.org/?id=DOID:14044 DOID:14044]

|

|

|

|-

| chronic salpingitis

| class of disease

| salpingitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5731 DOID:5731]

|

|

|

|-

| chronic salpingo-oophoritis

| class of disease

| salpingo-oophoritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12265 DOID:12265]

|

|

|

|-

| chronic sphenoidal sinusitis

| class of disease

| sphenoid sinusitis
chronic condition

| sphenoid sinusitis which lasts for 12 weeks or more

| [http://www.disease-ontology.org/?id=DOID:10793 DOID:10793]

|

|

|

|-

| chronic spontaneous urticaria

| class of disease

| chronic urticaria
idiopathic urticaria

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080749 DOID:0080749]

|

| Chronic spontaneous urticaria

| File:Chronic spontaneous urticaria.jpg

|-

| chronic subinvolution of uterus

| class of disease

| uterine disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13811 DOID:13811]

|

|

|

|-

| chronic toxic polyneuropathy

| class of disease

| chronic polyneuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7825 DOID:7825]

|

|

|

|-

| chronic tubotympanic suppurative otitis media

| class of disease

| chronic purulent otitis media
suppurative otitis media

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14435 DOID:14435]

|

|

|

|-

| chronic tympanitis

| class of disease

| tympanic membrane disease
myringitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11217 DOID:11217]

|

|

|

|-

| chronic ulcer of skin

| class of disease
symptom or sign

| skin disease
ulcer

| human disease

| [http://www.disease-ontology.org/?id=DOID:8549 DOID:8549]

|

|

|

|-

| chronic urticaria

| class of disease

| urticaria

| urticaria with symptoms lasting for more than 6 weeks

| [http://www.disease-ontology.org/?id=DOID:0080747 DOID:0080747]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.862.945.533 C17.800.862.945.533]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.904.533 C20.543.480.904.533]

|

|

|-

| chronic venous insufficiency

| class of disease

| venous insufficiency
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050853 DOID:0050853]

|

| Chronic venous insufficiency

|

|-

| chronic wasting disease

| class of disease

| animal disease
transmissible spongiform encephalopathy

| animal disease

| [http://www.disease-ontology.org/?id=DOID:3530 DOID:3530]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.228.800.858 C10.228.228.800.858]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.843.925 C10.574.843.925]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C22.955 C22.955]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.207.800.858 C01.207.800.858]

| Chronic wasting disease

| File:Deer1 tkreeger.jpg

|-

| chylocele of tunica vaginalis

| class of disease

| male reproductive system disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10835 DOID:10835]

|

|

|

|-

| cicatricial ectropion

| class of disease

| ectropion

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12782 DOID:12782]

|

|

|

|-

| cicatricial entropion

| class of disease

| entropion

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13113 DOID:13113]

|

|

|

|-

| cicatricial lagophthalmos

| class of disease

| lagophthalmos

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13038 DOID:13038]

|

|

|

|-

| cicatricial pemphigoid

| class of disease

| bullous skin disease
pemphigoid
eye inflammation
autoimmune disease of musculoskeletal system

| autoimmune blistering disease

| [http://www.disease-ontology.org/?id=DOID:11656 DOID:11656]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.187.482 C11.187.482]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.865.670 C17.800.865.670]

|

|

|-

| ciliary body cancer

| class of disease

| iris cancer
ciliary body neoplasm
ciliary body disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4352 DOID:4352]

|

|

|

|-

| ciliary body disease

| class of disease

| iris disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4353 DOID:4353]

|

|

|

|-

| citrullinemia type I

| class of disease

| citrullinemia

| medical condition

| [http://www.disease-ontology.org/?id=DOID:0070340 DOID:0070340]

|

|

|

|-

| classic congenital mesoblastic nephroma

| class of disease

| congenital mesoblastic nephroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8083 DOID:8083]

|

|

|

|-

| classic pulmonary blastoma

| class of disease

| pulmonary blastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4767 DOID:4767]

|

|

|

|-

| classic type lipoma

| class of disease

| lipoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10193 DOID:10193]

|

|

|

|-

| classic variant of chromophobe renal cell carcinoma

| class of disease

| chromophobe renal cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6605 DOID:6605]

|

|

|

|-

| clear cell acanthoma

| class of disease

| skin benign neoplasm
acanthoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:172 DOID:172]

|

|

|

|-

| clear cell adenocarcinoma

| class of disease

| adenocarcinoma
clear cell carcinoma

| adenocarcinoma that derives from epithelial cells which have clear cytoplasm

| [http://www.disease-ontology.org/?id=DOID:4468 DOID:4468]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.045 C04.557.470.200.025.045]

|

|

|-

| clear cell adenofibroma

| class of disease

| adenofibroma

| benign neoplasm characterized by the presence of glandular structures which contain clear cells and a fibrotic stroma

| [http://www.disease-ontology.org/?id=DOID:5477 DOID:5477]

|

|

|

|-

| clear cell adenoma

| class of disease

| adenoma

| adenoma that is composed of cells with a clear cytoplasm located in ovary

| [http://www.disease-ontology.org/?id=DOID:5390 DOID:5390]

|

|

|

|-

| clear cell basal cell carcinoma

| class of disease

| basal-cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4293 DOID:4293]

|

|

|

|-

| clear cell carcinoma

| class of disease

| carcinoma
connective tissue benign neoplasm
clear-cell tumor
sarcoma

| carcinoma (i.e. not a sarcoma) showing clear cells

| [http://www.disease-ontology.org/?id=DOID:4233 DOID:4233]

|

|

|

|-

| clear cell chondrosarcoma

| class of disease

| chondrosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5867 DOID:5867]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.280.140 C04.557.450.565.280.140]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.300.140 C04.557.450.795.300.140]

|

|

|-

| clear cell cystadenofibroma

| class of disease

| cystadenofibroma
clear cell adenofibroma

| benign neoplasm characterized by the presence of cystic glandular and fibrous tissues and clear cells

| [http://www.disease-ontology.org/?id=DOID:5895 DOID:5895]

|

|

|

|-

| clear cell ependymoma

| class of disease

| benign ependymoma

| ependymoma, often supratentorial in location, characterized by the presence of ependymal cells with a perinuclear halo

| [http://www.disease-ontology.org/?id=DOID:5507 DOID:5507]

|

|

|

|-

| clear cell hidradenoma

| class of disease

| hidradenoma
clear cell adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5443 DOID:5443]

|

|

|

|-

| clear cell meningioma

| class of disease

| meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4210 DOID:4210]

|

|

|

|-

| clear cell squamous cell skin carcinoma

| class of disease

| cutaneous squamous-cell carcinoma
clear cell carcinoma
keratinizing squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8288 DOID:8288]

|

|

|

|-

| clear cell variant infiltrating bladder urothelial carcinoma

| class of disease

| invasive bladder transitional cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6476 DOID:6476]

|

|

|

|-

| clear-cell ovarian carcinoma

| class of disease

| ovarian carcinoma
clear cell carcinoma
ovarian clear cell tumor

| ovarian carcinoma that has material basis in cells with clear cytoplasm and glycogen secreting hob nail cells

| [http://www.disease-ontology.org/?id=DOID:0050934 DOID:0050934]
[http://www.disease-ontology.org/?id=DOID:5305 DOID:5305]

|

| Clear-cell ovarian carcinoma

|

|-

| cleft lip

| class of disease

| lip disease
cleft lip and cleft palate

| human disease

| [http://www.disease-ontology.org/?id=DOID:9296 DOID:9296]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.409.225 C07.465.409.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.525.164 C07.465.525.164]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.650.525.164 C07.650.525.164]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.850.525.164 C16.131.850.525.164]

|

|

|-

| cleft palate

| class of disease

| cleft lip and cleft palate

| orofacial cleft characterized by a fissure of the soft and/or hard palate, due to faulty fusion of the two plates of the skull that form the hard palate

| [http://www.disease-ontology.org/?id=DOID:674 DOID:674]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.500.460.185 C05.500.460.185]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.660.207.540.460.185 C05.660.207.540.460.185]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.320.440.185 C07.320.440.185]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.525.185 C07.465.525.185]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.650.500.460.185 C07.650.500.460.185]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.650.525.185 C07.650.525.185]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.621.207.540.460.185 C16.131.621.207.540.460.185]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.850.500.460.185 C16.131.850.500.460.185]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.850.525.185 C16.131.850.525.185]

| Cleft palate

|

|-

| cleft soft palate

| class of disease

| cleft palate

| Cleft velum is a fissure type embryopathy that affects in varying degrees the soft palate

| [http://www.disease-ontology.org/?id=DOID:0110214 DOID:0110214]

|

|

|

|-

| clitoris cancer

| class of disease

| clitoris neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:2401 DOID:2401]

|

|

|

|-

| cloacogenic carcinoma

| class of disease

| anal squamous cell carcinoma
anal canal carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7173 DOID:7173]

|

|

|

|-

| co-trimoxazole allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger co-trimoxazole

| [http://www.disease-ontology.org/?id=DOID:0040070 DOID:0040070]

|

|

|

|-

| cobalt allergic asthma

| class of disease

| allergic asthma
cobalt allergy
metal allergy

| allergic asthma that has allergic trigger cobalt atom

| [http://www.disease-ontology.org/?id=DOID:0040054 DOID:0040054]

|

|

|

|-

| cobalt allergic contact dermatitis

| class of disease

| allergic contact dermatitis
cobalt allergy
metal allergy

| allergic contact dermatitis that has allergic trigger cobalt atom

| [http://www.disease-ontology.org/?id=DOID:0040053 DOID:0040053]

|

|

|

|-

| cobblestone retinal degeneration

| class of disease

| peripheral retinal degeneration

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12166 DOID:12166]

|

|

|

|-

| cocaine dependence

| class of disease

| cocaine-related disorder
substance dependence
substance abuse
disease

| drug dependence that is a psychological dependency on the regular use of cocaine

| [http://www.disease-ontology.org/?id=DOID:9975 DOID:9975]
[http://www.disease-ontology.org/?id=DOID:809 DOID:809]

|

|

|

|-

| coccidioidomycosis

| class of disease

| primary systemic mycosis
disease

| fungal infection

| [http://www.disease-ontology.org/?id=DOID:13450 DOID:13450]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.703.203 C01.150.703.203]

| Coccidioidomycosis

| File:Coccidioidomycosis granulomas on forehead.png

|-

| coenurosis

| class of disease

| parasitic helminthiasis infectious disease
Coenurosis
skin disease
central nervous system disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050251 DOID:0050251]

|

|

|

|-

| cognitive disorder

| class of disease

| mental disorder
organic brain syndrome

| disease of mental health that affects cognitive functions including memory processing, perception and problem solving

| [http://www.disease-ontology.org/?id=DOID:1561 DOID:1561]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.615.250 F03.615.250]

| Neurocognitive disorders

|

|-

| cold-induced sweating syndrome 1

| class of disease

| cold-induced sweating syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080329 DOID:0080329]

|

|

|

|-

| cold-induced sweating syndrome 2

| class of disease

| cold-induced sweating syndrome

| cold-induced sweating syndrome that has material basis in compound heterozygous mutation in the CLCF1 gene on chromosome 11q13

| [http://www.disease-ontology.org/?id=DOID:0080330 DOID:0080330]

|

|

|

|-

| cold-induced sweating syndrome 3; CISS3

| class of disease

| cold-induced sweating syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080331 DOID:0080331]

|

|

|

|-

| colitis

| class of disease

| inflammatory bowel diseases
colonic disease
disease

| inflammation of the colon or the large intestine

| [http://www.disease-ontology.org/?id=DOID:0060180 DOID:0060180]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.265 C06.405.205.265]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.158.188 C06.405.469.158.188]

| Colitis

| File:Cryptitis high mag.jpg

|-

| collagen disease

| class of disease

| connective tissue disease

| group of diseases affecting connective tissue

| [http://www.disease-ontology.org/?id=DOID:854 DOID:854]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.200 C17.300.200]

| Collagen diseases

|

|-

| collagenous colitis

| class of disease

| microscopic colitis
disease

| colitis characterized by a distinctive thickening of the subepithelial collagen table

| [http://www.disease-ontology.org/?id=DOID:0060183 DOID:0060183]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.265.173.500 C06.405.205.265.173.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.158.188.173.500 C06.405.469.158.188.173.500]

| Collagenous colitis

|

|-

| colloid adenoma

| class of disease

| follicular adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8419 DOID:8419]

|

|

|

|-

| colloid carcinoma of the pancreas

| class of disease

| pancreatic carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7717 DOID:7717]

|

|

|

|-

| coloboma of optic nerve

| class of disease

| coloboma
optic nerve disease
visual pathway disease

| rare defect of the optic nerve that causes moderate to severe visual field defects.

| [http://www.disease-ontology.org/?id=DOID:11975 DOID:11975]

|

|

|

|-

| colon adenocarcinoma

| class of disease

| colon carcinoma
adenocarcinoma

| colon carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:234 DOID:234]

|

|

| File:Metastatic colonic adenocarcinoma Case 165 (5477628150).jpg

|-

| colon adenoma

| class of disease

| colonic benign neoplasm
benign neoplasms by histologic type
colorectal adenoma
adenoma

| colonic benign neoplasm that has material basis in epithelial tissue with glandular origin

| [http://www.disease-ontology.org/?id=DOID:0050912 DOID:0050912]

|

|

|

|-

| colon carcinoma

| class of disease

| plump cancer
carcinoma

| colon cancer that has material basis in abnormally proliferating cells derives_from epithelial cells

| [http://www.disease-ontology.org/?id=DOID:1520 DOID:1520]

|

|

|

|-

| colon leiomyoma

| class of disease

| leiomyoma
colonic benign neoplasm
colonic disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10656 DOID:10656]

|

| Colonic leiomyoma

|

|-

| colon lymphoma

| class of disease

| plump cancer
lymphoma
colorectal lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1523 DOID:1523]

|

|

|

|-

| colon signet ring adenocarcinoma

| class of disease

| colon adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3033 DOID:3033]

|

|

|

|-

| colonic benign neoplasm

| class of disease

| intestinal benign neoplasm
colonic neoplasm
lymphangioma
colonic disease

| intestinal benign neoplasm that is located in the colon

| [http://www.disease-ontology.org/?id=DOID:235 DOID:235]

|

|

|

|-

| colonic disease

| class of disease

| intestinal disease

| pathological processes in the colon or large intestine

| [http://www.disease-ontology.org/?id=DOID:5353 DOID:5353]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.158 C06.405.469.158]

| Diseases and disorders of colon

|

|-

| colonic lymphangioma

| class of disease

| colonic benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10657 DOID:10657]

|

|

|

|-

| color agnosia

| class of disease

| agnosia
visual agnosia

| agnosia that is a loss of the ability to recognize a color, while being able to perceive or distinguish it

| [http://www.disease-ontology.org/?id=DOID:0060139 DOID:0060139]

|

|

|

|-

| color blindness

| class of disease

| vision disorder
colour vision deficiency
blindness
disease

| inability or decreased ability to see colour, or perceive colour differences, under normal lighting conditions

| [http://www.disease-ontology.org/?id=DOID:13399 DOID:13399]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.751.941.256 C10.597.751.941.256]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.966.256 C11.966.256]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.763.941.256 C23.888.592.763.941.256]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.270.151.500 C11.270.151.500]

| Color blindness

| File:Ishihara 9.svg

|-

| colorectal adenocarcinoma

| class of disease

| colorectal carcinoma
adenocarcinoma

| colorectal cancer that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:0050861 DOID:0050861]

|

| Colorectal adenocarcinoma

|

|-

| colorectal adenoma

| class of disease

| colonic benign neoplasm
gastrointestinal adenoma
colorectal polyp
intestinal benign neoplasm
adenoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050860 DOID:0050860]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.035.215 C04.557.470.035.215]

|

| File:Colon cancer.jpg

|-

| colorectal cancer

| class of disease

| colorectal neoplasm
large intestine cancer
disease

| cancer of the colon or rectum

| [http://www.disease-ontology.org/?id=DOID:9256 DOID:9256]

|

| Colorectal cancer

| File:Stomach colon rectum diagram-en.svg

|-

| colorectal carcinoma

| class of disease

| colorectal cancer
carcinoma

| colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa

| [http://www.disease-ontology.org/?id=DOID:0080199 DOID:0080199]

|

|

|

|-

| columnar cell variant papillary carcinoma

| class of disease

| papillary thyroid cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7088 DOID:7088]

|

|

|

|-

| combat disorder

| class of disease

| acute stress disorder
post-traumatic stress disorder
disease

| acute stress disorder that involves neurotic reactions to unusual, severe, or overwhelming military stress

| [http://www.disease-ontology.org/?id=DOID:6950 DOID:6950]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.950.750.249 F03.950.750.249]

| Combat stress reaction

|

|-

| combined T cell and B cell immunodeficiency

| class of disease

| combined immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:628 DOID:628]

|

|

|

|-

| combined cellular and humoral immune defects with granulomas

| class of disease

| autosomal recessive disease
combined immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112253 DOID:0112253]

|

|

|

|-

| combined oxidative phosphorylation deficiency 10

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111480 DOID:0111480]

|

|

|

|-

| combined oxidative phosphorylation deficiency 11

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111481 DOID:0111481]

|

|

|

|-

| combined oxidative phosphorylation deficiency 13

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111467 DOID:0111467]

|

|

|

|-

| combined oxidative phosphorylation deficiency 14

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111477 DOID:0111477]

|

|

|

|-

| combined oxidative phosphorylation deficiency 15

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111491 DOID:0111491]

|

|

|

|-

| combined oxidative phosphorylation deficiency 16

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111469 DOID:0111469]

|

|

|

|-

| combined oxidative phosphorylation deficiency 17

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111496 DOID:0111496]

|

|

|

|-

| combined oxidative phosphorylation deficiency 18

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111484 DOID:0111484]

|

|

|

|-

| combined oxidative phosphorylation deficiency 19

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111476 DOID:0111476]

|

|

|

|-

| combined oxidative phosphorylation deficiency 2

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111483 DOID:0111483]

|

|

|

|-

| combined oxidative phosphorylation deficiency 20

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111478 DOID:0111478]

|

|

|

|-

| combined oxidative phosphorylation deficiency 21

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111465 DOID:0111465]

|

|

|

|-

| combined oxidative phosphorylation deficiency 22

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111498 DOID:0111498]

|

|

|

|-

| combined oxidative phosphorylation deficiency 23

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111500 DOID:0111500]

|

|

|

|-

| combined oxidative phosphorylation deficiency 24

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111485 DOID:0111485]

|

|

|

|-

| combined oxidative phosphorylation deficiency 27

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111489 DOID:0111489]

|

|

|

|-

| combined oxidative phosphorylation deficiency 3

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111486 DOID:0111486]

|

|

|

|-

| combined oxidative phosphorylation deficiency 31

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111488 DOID:0111488]

|

|

|

|-

| combined oxidative phosphorylation deficiency 32

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111492 DOID:0111492]

|

|

|

|-

| combined oxidative phosphorylation deficiency 33

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

|

| [http://www.disease-ontology.org/?id=DOID:0111495 DOID:0111495]

|

|

|

|-

| combined oxidative phosphorylation deficiency 34

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111497 DOID:0111497]

|

|

|

|-

| combined oxidative phosphorylation deficiency 35

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111464 DOID:0111464]

|

|

|

|-

| combined oxidative phosphorylation deficiency 36

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111482 DOID:0111482]

|

|

|

|-

| combined oxidative phosphorylation deficiency 37

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111499 DOID:0111499]

|

|

|

|-

| combined oxidative phosphorylation deficiency 38

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111466 DOID:0111466]

|

|

|

|-

| combined oxidative phosphorylation deficiency 39

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111475 DOID:0111475]

|

|

|

|-

| combined oxidative phosphorylation deficiency 4

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111494 DOID:0111494]

|

|

|

|-

| combined oxidative phosphorylation deficiency 40

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112117 DOID:0112117]

|

|

|

|-

| combined oxidative phosphorylation deficiency 41

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112119 DOID:0112119]

|

|

|

|-

| combined oxidative phosphorylation deficiency 42

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112118 DOID:0112118]

|

|

|

|-

| combined oxidative phosphorylation deficiency 43

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112116 DOID:0112116]

|

|

|

|-

| combined oxidative phosphorylation deficiency 45

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112113 DOID:0112113]

|

|

|

|-

| combined oxidative phosphorylation deficiency 46

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112115 DOID:0112115]

|

|

|

|-

| combined oxidative phosphorylation deficiency 47

| class of disease

| combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112114 DOID:0112114]

|

|

|

|-

| combined oxidative phosphorylation deficiency 48

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112112 DOID:0112112]

|

|

|

|-

| combined oxidative phosphorylation deficiency 49

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112110 DOID:0112110]

|

|

|

|-

| combined oxidative phosphorylation deficiency 5

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111473 DOID:0111473]

|

|

|

|-

| combined oxidative phosphorylation deficiency 50

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112111 DOID:0112111]

|

|

|

|-

| combined oxidative phosphorylation deficiency 51

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112137 DOID:0112137]

|

|

|

|-

| combined oxidative phosphorylation deficiency 6

| class of disease

| combined oxidative phosphorylation deficiency
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111502 DOID:0111502]

|

|

|

|-

| combined oxidative phosphorylation deficiency 7

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111487 DOID:0111487]

|

|

|

|-

| combined oxidative phosphorylation deficiency 8

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111479 DOID:0111479]

|

|

|

|-

| combined oxidative phosphorylation deficiency 9

| class of disease

| autosomal recessive disease
combined oxidative phosphorylation deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111472 DOID:0111472]

|

|

|

|-

| combined thymoma

| class of disease

| thymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3281 DOID:3281]

|

|

|

|-

| comedocarcinoma

| class of disease

| intraductal carcinoma
disease

| carcinoma that is in situ

| [http://www.disease-ontology.org/?id=DOID:5670 DOID:5670]

|

|

|

|-

| commensal Klebsiella infectious disease

| class of disease

| klebsiellosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050479 DOID:0050479]

|

|

|

|-

| commensal bacterial infectious disease

| class of disease

| bacterial infectious disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050339 DOID:0050339]

|

|

|

|-

| common bile duct disease

| class of disease

| bile duct disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4137 DOID:4137]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.120.250 C06.130.120.250]

|

|

|-

| common bile duct neoplasm

| class of disease

| biliary tract neoplasm
common bile duct disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:4608 DOID:4608]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.120.250.250 C04.588.274.120.250.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.120.120.280 C06.130.120.120.280]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.120.250.280 C06.130.120.250.280]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.320.120.280 C06.130.320.120.280]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.120.250.250 C06.301.120.250.250]

|

|

|-

| common peroneal nerve lesion

| class of disease

| mononeuritis of lower limb

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12527 DOID:12527]

|

|

|

|-

| common wart

| class of disease

| viral infectious disease
wart

| viral infectious disease that results in infection located in skin, has material basis in human papillomavirus (types 2 and 4)

| [http://www.disease-ontology.org/?id=DOID:11165 DOID:11165]

|

| Verruca vulgaris

|

|-

| communicating hydrocephalus

| class of disease

| hydrocephalus

| abnormal accumulation of cerebrospinal fluid within the ventricles of the brain that occurs as a consequence of impaired cerebrospinal fluid reabsorption by the arachnoid granulations

| [http://www.disease-ontology.org/?id=DOID:1573 DOID:1573]

|

|

|

|-

| compartment syndrome

| class of disease

| ischemia
disease

| condition in which increased pressure within one of the body's compartments results in insufficient blood supply to tissue within that space

| [http://www.disease-ontology.org/?id=DOID:682 DOID:682]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.180 C05.651.180]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.303 C14.907.303]

| Compartment syndrome

| File:Fasciotomy leg.jpg

|-

| complement component 5 deficiency

| class of disease

| complement deficiency

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8158 DOID:8158]

|

|

|

|-

| complement component 6 deficiency

| class of disease

| complement deficiency

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060299 DOID:0060299]

|

|

|

|-

| complement component 7 deficiency

| class of disease

| complement deficiency

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060300 DOID:0060300]

|

|

|

|-

| complement deficiency

| class of disease

| primary immunodeficiency disease
metabolic disease

| primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation

| [http://www.disease-ontology.org/?id=DOID:626 DOID:626]

|

| Complement deficiencies

|

|-

| complete generalized lipodystrophy

| class of disease

| lipodystrophy

| lipodystrophy that is characterized by complete loss of adipose tissue

| [http://www.disease-ontology.org/?id=DOID:0080298 DOID:0080298]

|

|

|

|-

| complex cortical dysplasia with other brain malformations

| class of disease

| encephalopathy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0090131 DOID:0090131]

|

|

|

|-

| complex partial seizure

| class of disease
symptom or sign

| focal epilepsy
focal seizure

| human disease

| [http://www.disease-ontology.org/?id=DOID:12382 DOID:12382]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490.360.260 C10.228.140.490.360.260]

|

|

|-

| composite lymphoma

| class of disease

| B-cell lymphoma

| lymphoma that begins in cells of the immune system in which different types of lymphoma cells occur at the same time

| [http://www.disease-ontology.org/?id=DOID:5820 DOID:5820]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386.150 C04.557.386.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.435.295 C04.557.435.295]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.569.150 C15.604.515.569.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.761.150 C20.683.515.761.150]

|

|

|-

| conduct disorder

| class of disease

| specific developmental disorder
behavioral disorder
disease

| specific developmental disorder marked by a pattern of repetitive behavior wherein the rights of others or social norms are violated

| [http://www.disease-ontology.org/?id=DOID:12995 DOID:12995]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.625.094.300 F03.625.094.300]

|

|

|-

| cone-rod dystrophy

| class of disease

| retinal degeneration
monogenic disease

| retinal degeneration that characterized by progressive deterioration of the cone and rod photoreceptor cells

| [http://www.disease-ontology.org/?id=DOID:0050572 DOID:0050572]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.270.152 C11.270.152]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.768.585.658.250 C11.768.585.658.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.290.152 C16.320.290.152]

|

|

|-

| cone-rod dystrophy 1

| class of disease

| cone-rod dystrophy

| A cone-rod dystrophy that has material basis in variation in the chromosome region 18q21.1-q21.3.

| [http://www.disease-ontology.org/?id=DOID:0111009 DOID:0111009]

|

|

|

|-

| cone-rod dystrophy 17

| class of disease

| cone-rod dystrophy

| cone-rod dystrophy that has material basis in variation in the chromosome region 10q26

| [http://www.disease-ontology.org/?id=DOID:0111023 DOID:0111023]

|

|

|

|-

| cone-rod dystrophy 8

| class of disease

| cone-rod dystrophy

| cone-rod dystrophy that has material basis in variation in the chromosome region 1q12-q24

| [http://www.disease-ontology.org/?id=DOID:0111014 DOID:0111014]

|

|

|

|-

| congenital Zika virus infection

| class of disease

| Zika virus infection
vertically transmitted infection
syndrome
infectious embryofetopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080180 DOID:0080180]

|

|

|

|-

| congenital aphakia

| class of disease

| lens disease
aphakia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11367 DOID:11367]

|

|

|

|-

| congenital bile acid synthesis defect

| class of disease

| steroid inherited metabolic disorder
bile acid synthesis defect with cholestasis and malabsorption
congenital disorder

| steroid inherited metabolic disorder characterized by abnormal conversion of cholesterol into bile acids which occurs predominantly in the liver

| [http://www.disease-ontology.org/?id=DOID:0050674 DOID:0050674]

|

|

|

|-

| congenital chylothorax

| class of disease

| pleural disease
chylothorax
rare genetic respiratory disease
primary interstitial lung disease specific to childhood due to alveolar vascular disorder

| pleural disease characterized by the accumulation of chyle within the pleural space leading to respiratory distress, malnutrition and immunological compromise, either immediately after birth or within the first few weeks of life

| [http://www.disease-ontology.org/?id=DOID:0060646 DOID:0060646]

|

|

|

|-

| congenital diarrhea

| class of disease

| diarrhea
congenital disorder

| diarrhea characterized by frequent loose or liquid bowel movements where the disease is present from birth

| [http://www.disease-ontology.org/?id=DOID:0060774 DOID:0060774]

|

|

|

|-

| congenital disorder

| class of disease

| disease

| condition present at birth regardless of cause; human disease or disorder developed prior to birth

| [http://www.disease-ontology.org/?id=DOID:0080015 DOID:0080015]
[http://www.disease-ontology.org/?id=DOID:0060035 DOID:0060035]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16 C16]

| Congenital diseases and disorders

|

|-

| congenital disorder of glycosylation 1cc

| class of disease

| X-linked recessive disease
congenital disorder of glycosylation type I

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111839 DOID:0111839]

|

|

|

|-

| congenital disorder of glycosylation type I

| class of disease

| congenital disorder of glycosylation

| congenital disorder of glycosylation involve disrupted synthesis of the lipid-linked oligosaccharide precursor

| [http://www.disease-ontology.org/?id=DOID:0050570 DOID:0050570]

|

|

|

|-

| congenital disorder of glycosylation type IIa

| class of disease

| congenital disorder of glycosylation type II
autosomal recessive disease

| A congenital disorder of glycosylation type II that has material basis in an autosomal recessive mutation of MGAT2 on chromosome 14q21.3.

| [http://www.disease-ontology.org/?id=DOID:0070253 DOID:0070253]

|

|

|

|-

| congenital disorder of glycosylation type IIq

| class of disease

| congenital disorder of glycosylation type II
autosomal recessive disease

| A congenital disorder of glycosylation type II that has material basis in an autosomal recessive mutation of COG2 on chromosome 1q42.2.

| [http://www.disease-ontology.org/?id=DOID:0070269 DOID:0070269]

|

|

|

|-

| congenital disorder of glycosylation type Ia

| class of disease

| congenital disorder of glycosylation type I
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080552 DOID:0080552]

|

|

|

|-

| congenital dyserythropoietic anemia type I

| class of disease

| congenital dyserythropoietic anemia

| Congenital dyserythropoietic anemiatype I (CDA I) is a hematologic disorder of erythropoiesis characterized by moderate to severe macrocytic anemia occasionally associated with limb or nail deformities and scoliosis

| [http://www.disease-ontology.org/?id=DOID:0111396 DOID:0111396]

|

|

|

|-

| congenital dyserythropoietic anemia type II

| class of disease

| congenital dyserythropoietic anemia
autosomal recessive disease

| medical condition

| [http://www.disease-ontology.org/?id=DOID:0111401 DOID:0111401]

|

|

|

|-

| congenital dyserythropoietic anemia type III

| class of disease

| congenital dyserythropoietic anemia

| medical condition

| [http://www.disease-ontology.org/?id=DOID:0111399 DOID:0111399]

|

|

|

|-

| congenital dyserythropoietic anemia type IV

| class of disease

| congenital dyserythropoietic anemia
autosomal dominant disease

| medical condition

| [http://www.disease-ontology.org/?id=DOID:0111400 DOID:0111400]

|

|

|

|-

| congenital dyserythropoietic anemia type Ia

| class of disease

| autosomal recessive disease
congenital dyserythropoietic anemia type I

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111398 DOID:0111398]

|

|

|

|-

| congenital dyserythropoietic anemia type Ib

| class of disease

| autosomal recessive disease
congenital dyserythropoietic anemia type I

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111397 DOID:0111397]

|

|

|

|-

| congenital fiber-type disproportion

| class of disease

| congenital myopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0080102 DOID:0080102]

|

| Congenital fiber type disproportion

|

|-

| congenital fibrosarcoma

| class of disease

| pediatric fibrosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8418 DOID:8418]

|

|

|

|-

| congenital generalized lipodystrophy type 1

| class of disease

| congenital generalized lipodystrophy

| A congenital generalized lipodystrophy that has material basis in an autosomal recessive mutation of AGPAT2 on chromosome 9q34.3.

| [http://www.disease-ontology.org/?id=DOID:0111135 DOID:0111135]

|

|

|

|-

| congenital granular cell tumor

| class of disease

| mesenchymal cell neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8303 DOID:8303]

|

|

|

|-

| congenital heart block

| class of disease

| congenital heart disease
genetic cardiac rhythm disease
atrioventricular block
heart conduction disease

| atrioventricular block characterized by the presence of conduction system disease of any form, which is diagnosed on or before 28 days of life

| [http://www.disease-ontology.org/?id=DOID:990 DOID:990]

|

|

|

|-

| congenital hemolytic anemia

| class of disease
symptom or sign

| hemolytic anemia
congenital anemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:589 DOID:589]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.141.150 C15.378.071.141.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.070 C16.320.070]

|

|

|-

| congenital hypogammaglobulinemia

| class of disease

| B cell deficiency
agammaglobulinemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14177 DOID:14177]

|

|

|

|-

| congenital hypoplastic anemia

| class of disease

| aplastic anemia
congenital anemia
congenital bone marrow failure syndromes
congenital disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1342 DOID:1342]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.085.080 C15.378.071.085.080]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.190.223.500.500 C15.378.190.223.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.077 C16.320.077]

|

|

|-

| congenital hypothyroidism

| class of disease

| hypothyroidism
congenital disorder

| hypothyroidism that is present at birth

| [http://www.disease-ontology.org/?id=DOID:0050328 DOID:0050328]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.099.343.347 C05.116.099.343.347]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.132.256 C05.116.132.256]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.240.625 C16.320.240.625]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.297.155 C19.297.155]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.874.482.281 C19.874.482.281]

| Congenital hypothyroidism

| File:Jaundice in newborn.jpg

|-

| congenital intrinsic factor deficiency

| class of disease

| vitamin B12 deficiency
inborn disorder of cobalamin metabolism and transport
vitamin B12 deficiency anemia
congenital disorder

| vitamin B12 deficiency that is characterized by megaloblastic anemia due to the absence of gastric intrinsic factor which results in abnormal vitamin B12 absorption

| [http://www.disease-ontology.org/?id=DOID:0050734 DOID:0050734]

|

|

|

|-

| congenital lactase deficiency

| class of disease

| lactase deficiency
carbohydrate metabolic disorder
disorder of carbohydrate absorption and transport
congenital intestinal disease due to an enzymatic defect
metabolic disease with intestinal involvement
autosomal recessive disease

| rare severe gastrointestinal disorder in newborns primarily reported in Finland

| [http://www.disease-ontology.org/?id=DOID:0111646 DOID:0111646]

|

|

|

|-

| congenital limbs-face contractures-hypotonia-developmental delay syndrome

| class of disease

| syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0081048 DOID:0081048]

|

|

|

|-

| congenital megabladder

| class of disease

| bladder disease
autosomal dominant disease
Megacystis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112014 DOID:0112014]

|

|

|

|-

| congenital mesoblastic nephroma

| class of disease

| mesoblastic nephroma
kidney cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4773 DOID:4773]

|

|

|

|-

| congenital muscular dystrophy

| class of disease

| muscular dystrophy
autosomal recessive disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050557 DOID:0050557]

|

|

|

|-

| congenital muscular dystrophy 1B

| class of disease

| congenital muscular dystrophy
genetic disease
autosomal recessive disease

| congenital muscular dystrophy characterized by autosomal recessive inheritance of proximal muscle weakness, muscle hypertrophy, and early respiratory failure that has material basis in variation in the chromosome region 1q42

| [http://www.disease-ontology.org/?id=DOID:0110634 DOID:0110634]

|

|

|

|-

| congenital muscular dystrophy merosin-positive

| class of disease

| congenital muscular dystrophy
genetic disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110638 DOID:0110638]

|

|

|

|-

| congenital muscular dystrophy with cataracts and intellectual disability

| class of disease

| congenital muscular dystrophy
genetic disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080197 DOID:0080197]

|

|

|

|-

| congenital muscular dystrophy-dystroglycanopathy A14

| class of disease

| congenital muscular dystrophy-dystroglycanopathy type A

| A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in in GMPPB on 3p21.31.

| [http://www.disease-ontology.org/?id=DOID:0111233 DOID:0111233]

|

|

|

|-

| congenital muscular dystrophy-dystroglycanopathy A7

| class of disease

| congenital muscular dystrophy-dystroglycanopathy type A

| A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in ISPD on 7p21.2-p21.1.

| [http://www.disease-ontology.org/?id=DOID:0111234 DOID:0111234]

|

|

|

|-

| congenital muscular dystrophy-dystroglycanopathy type A

| class of disease

| muscular dystrophy-dystroglycanopathy

| muscular dystrophy-dystroglycanopathy characterized by cobblestone lissencephaly, muscle weakness, and brain and eye anomalies that has material basis in autosomal recessive inheritance a defect in alpha-dystroglycan post-translational processing

| [http://www.disease-ontology.org/?id=DOID:0111229 DOID:0111229]

|

|

|

|-

| congenital muscular dystrophy-dystroglycanopathy type A1

| class of disease

| congenital muscular dystrophy-dystroglycanopathy type A

| A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in POMT1 on 9q34.13.

| [http://www.disease-ontology.org/?id=DOID:0111237 DOID:0111237]

|

|

|

|-

| congenital muscular dystrophy-dystroglycanopathy type A10

| class of disease

| congenital muscular dystrophy-dystroglycanopathy type A

| A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in RXYLT1 on 12q14.2.

| [http://www.disease-ontology.org/?id=DOID:0111239 DOID:0111239]

|

|

|

|-

| congenital muscular dystrophy-dystroglycanopathy type A11

| class of disease

| congenital muscular dystrophy-dystroglycanopathy type A

| A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in B3GALNT2 on 1q42.3.

| [http://www.disease-ontology.org/?id=DOID:0111230 DOID:0111230]

|

|

|

|-

| congenital muscular dystrophy-dystroglycanopathy type A12

| class of disease

| congenital muscular dystrophy-dystroglycanopathy type A

| A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in POMK on 8p11.21.

| [http://www.disease-ontology.org/?id=DOID:0111235 DOID:0111235]

|

|

|

|-

| congenital muscular dystrophy-dystroglycanopathy type A13

| class of disease

| congenital muscular dystrophy-dystroglycanopathy type A

| A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in B4GAT1 on 11q13.2.

| [http://www.disease-ontology.org/?id=DOID:0111238 DOID:0111238]

|

|

|

|-

| congenital muscular dystrophy-dystroglycanopathy type A3

| class of disease

| congenital muscular dystrophy-dystroglycanopathy type A

| A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in POMGNT1 on 1p34.1.

| [http://www.disease-ontology.org/?id=DOID:0111236 DOID:0111236]

|

|

|

|-

| congenital muscular dystrophy-dystroglycanopathy type A5

| class of disease

| congenital muscular dystrophy-dystroglycanopathy type A

| A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in FKRP on 19q13.32.

| [http://www.disease-ontology.org/?id=DOID:0111241 DOID:0111241]

|

|

|

|-

| congenital muscular dystrophy-dystroglycanopathy type A6

| class of disease

| congenital muscular dystrophy-dystroglycanopathy type A

| A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in LARGE on 22q12.3.

| [http://www.disease-ontology.org/?id=DOID:0111242 DOID:0111242]

|

|

|

|-

| congenital muscular dystrophy-dystroglycanopathy type A8

| class of disease

| congenital muscular dystrophy-dystroglycanopathy type A

| A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in POMGNT2 on 3p22.1.

| [http://www.disease-ontology.org/?id=DOID:0111231 DOID:0111231]

|

|

|

|-

| congenital muscular dystrophy-dystroglycanopathy type A9

| class of disease

| congenital muscular dystrophy-dystroglycanopathy type A

| A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in DAG1 on 3p21.31.

| [http://www.disease-ontology.org/?id=DOID:0111232 DOID:0111232]

|

|

|

|-

| congenital myasthenic syndrome 10

| class of disease

| congenital myasthenic syndrome
genetic disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110668 DOID:0110668]

|

|

|

|-

| congenital myasthenic syndrome 1A

| class of disease

| congenital myasthenic syndrome
genetic disease
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110663 DOID:0110663]

|

|

|

|-

| congenital nongoitrous hypothryoidism 1

| class of disease

| hypothyroidism, congenital, nongoitrous
genetic disease
autosomal recessive disease

| congenital hypothyroidism that has material basis in mutation in the TSHR gene on chromosome 14q31

| [http://www.disease-ontology.org/?id=DOID:0070126 DOID:0070126]

|

|

|

|-

| congenital nongoitrous hypothryoidism 2

| class of disease

| hypothyroidism, congenital, nongoitrous
congenital hypothyroidism due to developmental anomaly
congenital thyroid malformation without hypothyroidism
thyroid hormone resistance syndrome
genetic disease
autosomal dominant disease

| congenital hypothyroidism that has material basis in heterozygous mutation in the PAX8 gene on chromosome 2q13

| [http://www.disease-ontology.org/?id=DOID:0070124 DOID:0070124]

|

|

|

|-

| congenital nongoitrous hypothryoidism 3

| class of disease

| hypothyroidism, congenital, nongoitrous
genetic disease
autosomal dominant disease

| A congenital hypothyroidism characterized by autosomal dominant inheritance of resistance to thyrotropin that has material basis in variation in the chromosome region 15q25.3-q26.1.

| [http://www.disease-ontology.org/?id=DOID:0070127 DOID:0070127]

|

|

|

|-

| congenital nongoitrous hypothryoidism 4

| class of disease

| hypothyroidism, congenital, nongoitrous
genetic disease
autosomal recessive disease

| congenital hypothyroidism characterized by a permanent thyroid deficiency present at birth and resulting from deficiency in TSH synthesis that has material basis in homozygous mutation in the TSHB gene on chromosome 1p13

| [http://www.disease-ontology.org/?id=DOID:0070123 DOID:0070123]

|

|

|

|-

| congenital nongoitrous hypothryoidism 5

| class of disease

| hypothyroidism, congenital, nongoitrous
genetic disease
autosomal dominant disease
congenital hypothyroidism

| congenital hypothyroidism that has material basis in heterozygous mutation in the NKX2-5 gene on chromosome 5q35

| [http://www.disease-ontology.org/?id=DOID:0070125 DOID:0070125]

|

|

|

|-

| congenital nongoitrous hypothryoidism 6

| class of disease

| hypothyroidism, congenital, nongoitrous
genetic disease
autosomal dominant disease

| A congenital hypothyroidism that has material basis in heterozygous mutation in the THRA gene on chromosome 17q21.1.

| [http://www.disease-ontology.org/?id=DOID:0070128 DOID:0070128]

|

|

|

|-

| congenital nongoitrous hypothyroidism 7

| class of disease

| autosomal recessive disease
hypothyroidism, congenital, nongoitrous

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111836 DOID:0111836]

|

|

|

|-

| congenital nongoitrous hypothyroidism 8

| class of disease

| autosomal dominant disease
hypothyroidism, congenital, nongoitrous

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111837 DOID:0111837]

|

|

|

|-

| congenital nongoitrous hypothyroidism 9

| class of disease

| X-linked recessive disease
hypothyroidism, congenital, nongoitrous

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111835 DOID:0111835]

|

|

|

|-

| congenital nystagmus 1

| class of disease

| autosomal genetic disease
congenital nystagmus

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111790 DOID:0111790]

|

|

|

|-

| congenital nystagmus 2

| class of disease

| congenital nystagmus
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111792 DOID:0111792]

|

|

|

|-

| congenital nystagmus 3

| class of disease

| autosomal dominant disease
congenital nystagmus

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111793 DOID:0111793]

|

|

|

|-

| congenital nystagmus 4

| class of disease

| congenital nystagmus
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111794 DOID:0111794]

|

|

|

|-

| congenital nystagmus 5

| class of disease

| X-linked dominant disease
congenital nystagmus

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111796 DOID:0111796]

|

|

|

|-

| congenital nystagmus 6

| class of disease

| congenital nystagmus

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111795 DOID:0111795]

|

|

|

|-

| congenital nystagmus 7

| class of disease

| autosomal dominant disease
congenital nystagmus

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111791 DOID:0111791]

|

|

|

|-

| congenital ptosis

| class of disease

| ptosis

| ptosis characterized by eyelid drop present at birth

| [http://www.disease-ontology.org/?id=DOID:0060261 DOID:0060261]

|

|

|

|-

| congenital stationary night blindness

| class of disease

| hereditary night blindness

| night blindness that is characterized by hemeralopia with a moderate loss of visual acuity and caused by defective photoreceptor-to-bipolar cell signaling with common ERG findings of reduced or absent b-waves and generally normal a-waves

| [http://www.disease-ontology.org/?id=DOID:0050534 DOID:0050534]

|

|

|

|-

| congenital stationary night blindness 1A

| class of disease

| congenital stationary night blindness
X-linked recessive disease

| A congenital stationary night blindness that has material basis in mutation in the NYX gene on chromosome Xp11.4.

| [http://www.disease-ontology.org/?id=DOID:0110870 DOID:0110870]

|

|

|

|-

| congenital stationary night blindness 2A

| class of disease

| congenital stationary night blindness
X-linked recessive disease

| A congenital stationary night blindness that has material basis in mutation in the CACNA1F gene on chromosome Xp11.23.

| [http://www.disease-ontology.org/?id=DOID:0110871 DOID:0110871]

|

|

|

|-

| congenital structural myopathy

| class of disease

| muscular disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:422 DOID:422]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.575 C05.651.575]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.491.550 C10.668.491.550]

|

|

|-

| congenital symmetric circumferential skin creases 1

| class of disease

| autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112242 DOID:0112242]

|

|

|

|-

| congestive heart failure

| class of disease

| heart disease
heart failure

| human disease

| [http://www.disease-ontology.org/?id=DOID:6000 DOID:6000]

|

|

|

|-

| conidiobolomycosis

| class of disease

| subcutaneous mycosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050279 DOID:0050279]

|

|

|

|-

| conjugate gaze palsy

| class of disease

| strabismus
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12445 DOID:12445]

|

|

|

|-

| conjunctival cancer

| class of disease

| ocular cancer
conjunctival neoplasm
conjunctival disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5467 DOID:5467]

|

|

|

|-

| conjunctival concretion

| class of disease

| conjunctival deposit

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11988 DOID:11988]

|

|

|

|-

| conjunctival degeneration

| class of disease

| conjunctival disease
conjunctival degenerations and deposits
eye degenerative disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10139 DOID:10139]

|

|

|

|-

| conjunctival deposit

| class of disease

| conjunctival disease
conjunctival degenerations and deposits

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11653 DOID:11653]

|

|

|

|-

| conjunctival disease

| class of disease

| eye disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4251 DOID:4251]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.187 C11.187]

|

|

|-

| conjunctival folliculosis

| class of disease

| acute conjunctivitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11219 DOID:11219]

|

|

|

|-

| conjunctival pigmentation

| class of disease

| pigmentation disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12304 DOID:12304]

|

|

|

|-

| conjunctival pterygium

| class of disease

| conjunctival degeneration
pterygium

| human disease

| [http://www.disease-ontology.org/?id=DOID:10526 DOID:10526]

|

|

|

|-

| conjunctival vascular disease

| class of disease

| conjunctival disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10989 DOID:10989]

|

|

|

|-

| conjunctivochalasis

| class of disease

| conjunctival disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4250 DOID:4250]

|

| Conjunctivochalasis

|

|-

| connective tissue benign neoplasm

| class of disease

| musculoskeletal system benign neoplasm
connective tissue disease
connective tissue neoplasm

| musculoskeletal system benign neoplasm that is located in connective tissue

| [http://www.disease-ontology.org/?id=DOID:0060123 DOID:0060123]

|

|

|

|-

| connective tissue disease

| class of disease

| musculoskeletal disorder
skin and connective tissue diseases

| musculoskeletal system disease that affects tissues such as skin, tendons, and cartilage

| [http://www.disease-ontology.org/?id=DOID:65 DOID:65]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300 C17.300]

| Connective tissue diseases

|

|-

| connective tissue neoplasm

| class of disease

| musculoskeletal system cancer
connective tissue disease
connective and soft tissue neoplasms

| musculoskeletal system cancer that is located in connective tissue

| [http://www.disease-ontology.org/?id=DOID:201 DOID:201]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565 C04.557.450.565]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.680 C17.300.680]

|

|

|-

| constant exophthalmos

| class of disease

| orbital disease
exophthalmos

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9945 DOID:9945]

|

|

|

|-

| constipation

| class of disease
symptom or sign

| bowel dysfunction
clinical sign
feces and droppings symptom
disease

| bowel dysfunction that is characterized by infrequent or difficult evacuation of feces

| [http://www.disease-ontology.org/?id=DOID:2089 DOID:2089]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.821.150 C23.888.821.150]

| Constipation

|

|-

| constrictive pericarditis

| class of disease

| pericarditis

| heart disorder in which the pericardial sac becomes thickened and fibrotic, tightening the myocardium and impeding the normal myocardial function

| [http://www.disease-ontology.org/?id=DOID:11481 DOID:11481]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.720.595 C14.280.720.595]

| Constrictive pericarditis

| File:Constrictive pericarditis.jpg

|-

| contact blepharoconjunctivitis

| class of disease

| blepharoconjunctivitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13999 DOID:13999]

|

|

|

|-

| contact dermatitis

| class of disease

| dermatitis
eczema
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:2773 DOID:2773]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.174.255 C17.800.174.255]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.815.255 C17.800.815.255]

| Contact dermatitis

| File:Contact dermatitis.jpg

|-

| contact lens corneal edema

| class of disease

| corneal edema

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11034 DOID:11034]

|

|

|

|-

| conus medullaris neoplasm

| class of disease

| Spinal cord cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3641 DOID:3641]

|

|

|

|-

| conventional angiosarcoma

| class of disease

| angiosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4512 DOID:4512]

|

|

|

|-

| conventional central osteosarcoma

| class of disease

| bone osteosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3378 DOID:3378]

|

|

|

|-

| conventional fibrosarcoma

| class of disease

| fibrosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3517 DOID:3517]

|

|

|

|-

| conventional leiomyosarcoma

| class of disease

| leiomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5253 DOID:5253]

|

|

|

|-

| conventional malignant hemangiopericytoma

| class of disease

| hemangiopericytoma
hemangiopericytoma, malignant

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6197 DOID:6197]

|

|

|

|-

| conversion disorder

| class of disease
symptom or sign

| somatoform disorder
functional neurologic disorder
disease

| physical illness or symptoms caused by serious emotional stress

| [http://www.disease-ontology.org/?id=DOID:1768 DOID:1768]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.875.300 F03.875.300]

|

|

|-

| cor pulmonale

| class of disease

| congestive heart failure
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:8515 DOID:8515]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.832 C14.280.832]

| Pulmonary heart disease

|

|-

| core binding factor acute myeloid leukemia

| class of disease

| acute myeloid leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080796 DOID:0080796]

|

|

|

|-

| cork-handlers' disease

| class of disease

| extrinsic allergic alveolitis

| An extrinsic allergic alveolitis caused by inhalation of cork dust containing the antigens produced by the fungus Penicillium glabrum. The symptoms include dyspnea, wheezing cough, fever and asthenia.

| [http://www.disease-ontology.org/?id=DOID:840 DOID:840]

|

|

|

|-

| cornea cancer

| class of disease

| ocular cancer
cornea neoplasm
corneal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6199 DOID:6199]

|

|

|

|-

| cornea plana

| class of disease

| corneal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060287 DOID:0060287]

|

|

|

|-

| cornea squamous cell carcinoma

| class of disease

| cornea cancer
squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13538 DOID:13538]

|

|

|

|-

| corneal abscess

| class of disease

| deep keratitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11543 DOID:11543]

|

|

|

|-

| corneal argyrosis

| class of disease

| corneal disease
argyria

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13447 DOID:13447]

|

|

|

|-

| corneal degeneration

| class of disease

| corneal disease
eye degenerative disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1237 DOID:1237]

|

|

|

|-

| corneal deposit

| class of disease

| corneal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11547 DOID:11547]

|

|

|

|-

| corneal disease

| class of disease

| eye disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:10124 DOID:10124]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.204 C11.204]

| Disorders of sclera and cornea

|

|-

| corneal dystrophy

| class of disease

| corneal disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:2566 DOID:2566]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.204.236 C11.204.236]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.270.162 C11.270.162]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.290.162 C16.320.290.162]

| Corneal dystrophy

|

|-

| corneal ectasia

| class of disease

| corneal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1436 DOID:1436]

|

|

|

|-

| corneal edema

| class of disease

| corneal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11030 DOID:11030]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.204.267 C11.204.267]

|

|

|-

| corneal endothelial dystrophy

| class of disease

| corneal dystrophy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060443 DOID:0060443]

|

|

|

|-

| corneal granular dystrophy

| class of disease

| epithelial-stromal TGFBI dystrophy
autosomal dominant disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12318 DOID:12318]

|

| Granular corneal dystrophy

|

|-

| corneal neovascularization

| class of disease

| keratitis
neovascularization

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11382 DOID:11382]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.204.290 C11.204.290]

| Corneal neovascularization

|

|-

| corneal opacification and other ocular anomalies

| class of disease

| sclerocornea
genetic disease
monogenic disease
eye disease

| sclerocornea that has material basis in homozygous or compound heterozygous mutation in the PXDN gene on chromosome 2p25 and is characterized by corneal opacifiaction, cataract, microcornea, microphthalmia, and anterior segment dysgenesis

| [http://www.disease-ontology.org/?id=DOID:0060648 DOID:0060648]

|

|

|

|-

| corneal staphyloma

| class of disease

| corneal disease
staphyloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12753 DOID:12753]

|

|

|

|-

| corneal ulcer

| class of disease
symptom or sign

| keratitis
corneal disease
eye ulceration
cornea symptom
disease

| area of epithelial tissue loss from corneal surface; associated with inflammatory cells in the cornea and anterior chamber

| [http://www.disease-ontology.org/?id=DOID:8463 DOID:8463]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.539.375.177 C01.539.375.177]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.204.564.225 C11.204.564.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.294.177 C11.294.177]

| Corneal ulcer

|

|-

| coronary aneurysm

| class of disease

| aneurysm
aneurysm of heart
coronary artery disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3362 DOID:3362]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.647.250.250 C14.280.647.250.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.055.395 C14.907.055.395]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.585.250.250 C14.907.585.250.250]

| Coronary aneurysm

|

|-

| coronary artery anomaly

| class of disease

| coronary artery disease
vascular malformation
congenital heart disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11843 DOID:11843]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.240.400.210 C14.240.400.210]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.400.210 C14.280.400.210]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.240.400.210 C16.131.240.400.210]

| Coronary artery anomalies

|

|-

| coronary artery disease

| class of disease

| artery disease
cardiovascular disease
disease

| disease characterized by plaque building up in the arteries of the heart

| [http://www.disease-ontology.org/?id=DOID:3393 DOID:3393]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.647.250.260 C14.280.647.250.260]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.137.126.339 C14.907.137.126.339]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.585.250.260 C14.907.585.250.260]

| Coronary artery disease

| File:Blausen 0257 CoronaryArtery Plaque.png

|-

| coronary artery vasospasm

| class of disease

| coronary artery disease
vasospasm
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11840 DOID:11840]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.647.250.295 C14.280.647.250.295]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.585.250.295 C14.907.585.250.295]

|

|

|-

| coronary restenosis

| class of disease

| coronary stenosis
restenosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4247 DOID:4247]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.647.250.285.200 C14.280.647.250.285.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.585.250.285.200 C14.907.585.250.285.200]

|

|

|-

| coronary stenosis

| class of disease

| coronary artery disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4248 DOID:4248]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.647.250.285 C14.280.647.250.285]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.585.250.285 C14.907.585.250.285]

|

|

|-

| coronary thrombosis

| class of disease

| coronary artery disease
thrombosis
arterial thrombosis
disease

| disease: formation of a blood clot inside a blood vessel of the heart, which clot may then restrict blood flow within the heart, leading to heart tissue damage, or a myocardial infarction, also known as a heart attack

| [http://www.disease-ontology.org/?id=DOID:11847 DOID:11847]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.647.250.290 C14.280.647.250.290]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.355.830.220 C14.907.355.830.220]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.585.250.290 C14.907.585.250.290]

| Cardiac thrombosis

|

|-

| corpus callosum lipoma

| class of disease

| cerebral hemisphere lipoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6294 DOID:6294]

|

|

|

|-

| corpus callosum oligodendroglioma

| class of disease

| brain oligodendroglioma
oligodendroglioma

| brain oligodendroglioma located in the corpus callosum

| [http://www.disease-ontology.org/?id=DOID:0050901 DOID:0050901]

|

|

|

|-

| corpus luteum cyst

| class of disease

| ovarian cyst

| human disease

| [http://www.disease-ontology.org/?id=DOID:13050 DOID:13050]

|

|

|

|-

| cortical deafness

| class of disease

| sensorineural hearing loss
agnosia
central auditory disease
auditory agnosia

| agnosia that is a loss of the ability to perceive any auditory information but whose hearing is intact

| [http://www.disease-ontology.org/?id=DOID:0060140 DOID:0060140]

|

|

|

|-

| cortical senile cataract

| class of disease

| senile cataract

| human disease

| [http://www.disease-ontology.org/?id=DOID:13574 DOID:13574]

|

|

|

|-

| cortical thymoma

| class of disease

| dendritic cell thymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6530 DOID:6530]

|

|

|

|-

| corticosteroid allergy

| class of disease

| drug allergy
steroids allergy

| drug allergy that has allergic trigger corticosteroid

| [http://www.disease-ontology.org/?id=DOID:0040014 DOID:0040014]

|

|

|

|-

| corticosterone methyloxidase deficiency 1

| class of disease

| autosomal recessive disease
adrenal gland disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080626 DOID:0080626]

|

|

|

|-

| cortisone reductase deficiency

| class of disease

| endocrine system disease
hyperandrogenism

| endocrine system disease characterized by failure to regenerate the active glucocorticoid cortisol from cortisone resulting in adrenal hyperandrogenism

| [http://www.disease-ontology.org/?id=DOID:0090139 DOID:0090139]

|

|

|

|-

| costochondritis

| class of disease

| chondropathy
syndrome
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:14021 DOID:14021]

|

|

|

|-

| cough variant asthma

| class of disease

| asthma
chronic asthma

| asthma that is characterized by chronic nonproductive cough without shortness of breath

| [http://www.disease-ontology.org/?id=DOID:12323 DOID:12323]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.127.108.784 C08.127.108.784]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.495.108.750 C08.381.495.108.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.674.095.784 C08.674.095.784]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.680.095.688 C20.543.480.680.095.688]

|

|

|-

| cow milk allergy

| class of disease

| milk allergy

| milk allergy triggered by Bos taurus milk

| [http://www.disease-ontology.org/?id=DOID:0060521 DOID:0060521]

|

|

|

|-

| cranial nerve III tumor

| class of disease

| third cranial nerve disease
cranial nerve neoplasm
peripheral nervous system neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2817 DOID:2817]

|

|

|

|-

| cranial nerve disease

| class of disease

| peripheral neuropathy

| neuropathy that is located in one of the twelve cranial nerves

| [http://www.disease-ontology.org/?id=DOID:5656 DOID:5656]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292 C10.292]

|

|

|-

| cranial nerve neoplasm

| class of disease

| nervous system neoplasm
cranial nerve disease
central nervous system cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:338 DOID:338]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.614.300 C04.588.614.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.614.596.240 C04.588.614.596.240]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.225 C10.292.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.551.360 C10.551.360]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.551.775.250 C10.551.775.250]

| Cranial nerve neoplasms

|

|-

| cranial nerve palsy

| class of disease
symptom or sign

| cranial nerve disease
palsy
eye symptom

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3817 DOID:3817]

|

|

|

|-

| cranial pseudosarcomatous fasciitis

| class of disease

| pseudosarcomatous fibromatosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7326 DOID:7326]

|

|

|

|-

| cranio-facial dystonia

| class of disease

| focal dystonia

| focal dystonia that is characterized as dystonia that affects the muscles of the head, face, and neck

| [http://www.disease-ontology.org/?id=DOID:0050845 DOID:0050845]

|

|

|

|-

| craniodiaphyseal dysplasia

| class of disease

| osteosclerosis

| osteosclerosis that results in increased calcium concentration located in skull which decreases the size of cranium foramina and cervical spinal canal

| [http://www.disease-ontology.org/?id=DOID:0080032 DOID:0080032]

|

|

|

|-

| cranioectodermal dysplasia 1

| class of disease

| Sensenbrenner syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080803 DOID:0080803]

|

|

|

|-

| cranioectodermal dysplasia 2

| class of disease

| Sensenbrenner syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080804 DOID:0080804]

|

|

|

|-

| cranioectodermal dysplasia 3

| class of disease

| Sensenbrenner syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080805 DOID:0080805]

|

|

|

|-

| cranioectodermal dysplasia 4

| class of disease

| Sensenbrenner syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080806 DOID:0080806]

|

|

|

|-

| craniopharyngioma

| class of disease

| central nervous system organ benign neoplasm
Rathke's pouch tumor

| type of brain tumor derived from pituitary gland embryonic tissue that occurs most commonly in children, but also affects adults

| [http://www.disease-ontology.org/?id=DOID:3840 DOID:3840]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.200 C04.557.465.625.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.200 C04.557.580.625.200]

| Craniopharyngiomas

| File:Adamantinomatous craniopharyngioma - very low mag.jpg

|-

| craniosynostosis

| class of disease

| synostosis
rare disease
craniofacial disease
disease

| premature fusion of bones in the skull

| [http://www.disease-ontology.org/?id=DOID:2340 DOID:2340]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.099.370.894.232 C05.116.099.370.894.232]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.660.207.240 C05.660.207.240]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.660.906.364 C05.660.906.364]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.621.207.240 C16.131.621.207.240]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.621.906.364 C16.131.621.906.364]

| Craniosynostosis

| File:Cranialsynostosis.jpg

|-

| crater-like holes of optic disc

| class of disease

| visual pathway disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13295 DOID:13295]

|

| Optic pit

|

|-

| crescentic glomerulonephritis

| class of disease

| acute proliferative glomerulonephritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13139 DOID:13139]

|

|

|

|-

| cribriform carcinoma

| class of disease

| breast carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5675 DOID:5675]

|

|

|

|-

| cribriform variant testicular seminoma

| class of disease

| testis seminoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7269 DOID:7269]

|

|

|

|-

| critical illness polyneuropathy

| class of disease

| inflammatory and toxic neuropathy
polyneuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14402 DOID:14402]

|

|

|

|-

| crustacean allergy

| class of disease

| shellfish allergy
seafood allergy

| shellfish allergy triggered by Crustacea

| [http://www.disease-ontology.org/?id=DOID:0060524 DOID:0060524]

|

|

|

|-

| cryptococcal meningitis

| class of disease

| cryptococcosis
fungal meningitis

| fungal meningitis that has material basis in Crypococcus fungal infection

| [http://www.disease-ontology.org/?id=DOID:0080159 DOID:0080159]
[http://www.disease-ontology.org/?id=DOID:12052 DOID:12052]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.703.181.500.500 C01.150.703.181.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.703.248.290 C01.150.703.248.290]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.228.198.500.500 C10.228.228.198.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.586.625.300.500 C10.586.625.300.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.207.198.500.500 C01.207.198.500.500]

| Meningeal cryptococcosis

|

|-

| cryptophthalmos

| class of disease

| eyelid disease
congenital disorder

| congenital abnormality characterized by the presence of a continuous layer of skin extending over the eyeballs and the absence of eyelids and the palpebral fissure

| [http://www.disease-ontology.org/?id=DOID:0111716 DOID:0111716]

|

|

|

|-

| cryptorchidism

| class of disease

| congenital disorder
testicular disease
male reproductive system disease
genetic disease
sex differentiation disease
disease

| defective mammal development

| [http://www.disease-ontology.org/?id=DOID:11383 DOID:11383]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.294.829.258 C12.200.294.829.258]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.706.258 C12.200.706.258]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.258 C16.131.939.258]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.829.258 C19.391.829.258]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.100.500.829.258 C12.100.500.829.258]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.800.258 C12.800.258]

| Cryptorchidism

|

|-

| cutaneous Paget's disease

| class of disease

| skin carcinoma
extramammary Paget's disease

| skin carcinoma that is characterized by infiltration of the skin by neoplastic large cells with abundant pale cytoplasm and large nuclei with prominent nucleoli

| [http://www.disease-ontology.org/?id=DOID:3450 DOID:3450]

|

|

|

|-

| cutaneous T cell lymphoma

| class of disease

| peripheral T-cell lymphoma
genetic disease
cutaneous lymphoma
disease

| non-Hodgkin's lymphoma that has material basis in a mutation of T cells

| [http://www.disease-ontology.org/?id=DOID:0060061 DOID:0060061]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386.480.750.800 C04.557.386.480.750.800]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.569.480.750.800 C15.604.515.569.480.750.800]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.761.480.750.800 C20.683.515.761.480.750.800]

| Cutaneous T-cell lymphoma

|

|-

| cutaneous candidiasis

| class of disease
symptom or sign

| dermatomycosis
candidiasis
skin disease

| candidiasis that is characterized by Candida infection located in the skin

| [http://www.disease-ontology.org/?id=DOID:0080161 DOID:0080161]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.703.160.132 C01.150.703.160.132]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.703.302.105 C01.150.703.302.105]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.800.200.105 C01.800.200.105]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.838.208.170 C17.800.838.208.170]

| Candidiasis of the skin

|

|-

| cutaneous diphtheria

| class of disease

| pyoderma
diphtheria

| pyoderma that is a milder form of diphtheria restricted to the skin producing shallow skin ulcers is caused by direct physical contact of individuals infected with Corynebacterium diphtheriae as the bacteria releases the diphtheria toxin

| [http://www.disease-ontology.org/?id=DOID:12275 DOID:12275]

|

|

|

|-

| cutaneous endometriosis

| class of disease

| endometriosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:11430 DOID:11430]

|

|

|

|-

| cutaneous ganglioneuroma

| class of disease

| skin benign neoplasm
ganglioneuroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2425 DOID:2425]

|

|

|

|-

| cutaneous leiomyosarcoma

| class of disease

| skin sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5273 DOID:5273]

|

| Cutaneous leiomyosarcoma

|

|-

| cutaneous liposarcoma

| class of disease

| skin sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5712 DOID:5712]

|

|

|

|-

| cutaneous lupus erythematosus

| class of disease

| lupus erythematosus
skin disease

| lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight

| [http://www.disease-ontology.org/?id=DOID:0050169 DOID:0050169]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.475 C17.300.475]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.480 C17.800.480]

|

|

|-

| cutaneous mastocytosis

| class of disease

| mastocytosis
skin disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3663 DOID:3663]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.465.500 C04.557.450.565.465.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.508.473 C17.800.508.473]

|

|

|-

| cutaneous meningioma

| class of disease

| skin benign neoplasm
ectopic meningioma
skin cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8006 DOID:8006]

|

|

|

|-

| cutaneous mucoepidermoid carcinoma

| class of disease

| skin benign neoplasm
mucoepidermoid carcinoma
skin carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4683 DOID:4683]

|

|

|

|-

| cutaneous small-vessel vasculitis

| class of disease

| hypersensitivity vasculitis
skin disease
microvasculitis
allergy
disease

| hypersensitivity vasculitis that results in inflammation of small blood vessels, characterized clinically by palpable purpura, which is a slightly elevated purpuric rash over one or more areas of the skin

| [http://www.disease-ontology.org/?id=DOID:11450 DOID:11450]

|

| Cutaneous small-vessel vasculitis

|

|-

| cutaneous squamous-cell carcinoma

| class of disease

| skin carcinoma
squamous cell carcinoma
disease

| skin carcinoma that has material basis in squamous cells

| [http://www.disease-ontology.org/?id=DOID:3151 DOID:3151]

|

| Squamous-cell carcinoma of the skin

|

|-

| cyclophosphamide allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger cyclophosphamide

| [http://www.disease-ontology.org/?id=DOID:0040027 DOID:0040027]

|

|

|

|-

| cycloplegia

| class of disease

| eye accommodation disease
disease

| paralysis of the ciliary muscle of the eye, resulting in a loss of accommodation

| [http://www.disease-ontology.org/?id=DOID:10033 DOID:10033]

|

|

|

|-

| cyclothymia

| class of disease

| bipolar disorder
disease

| persistent instability of mood that involves recurrent hypomanic and dysthymic episodes, but no full manic episodes or full major depressive episodes

| [http://www.disease-ontology.org/?id=DOID:845 DOID:845]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.600.500 F03.600.500]

|

|

|-

| cyclotropia

| class of disease

| strabismus

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9838 DOID:9838]

|

|

|

|-

| cylindrical spirals myopathy

| class of disease

| congenital myopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0080103 DOID:0080103]

|

|

|

|-

| cystadenocarcinoma

| class of disease

| cystic neoplasm
malignant cystadenoma
disease

| adenocarcinoma that derives from epithelial cells originating in glandular tissue, in which cystic accumulations of retained secretions are formed

| [http://www.disease-ontology.org/?id=DOID:3111 DOID:3111]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.480 C04.557.470.200.025.480]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.590.480 C04.557.470.590.480]

|

| File:Mucinous lmp ovarian tumour intermed mag.jpg

|-

| cystadenofibroma

| class of disease

| adenofibroma
ovarian benign neoplasm

| adenofibroma composed of epithelial ovarian tissue

| [http://www.disease-ontology.org/?id=DOID:5482 DOID:5482]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.590.595.050.500 C04.557.450.565.590.595.050.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.590.482 C04.557.470.590.482]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.625.050.500 C04.557.470.625.050.500]

|

|

|-

| cystadenoma

| class of disease

| adenoma

| adenoma that is a cystic

| [http://www.disease-ontology.org/?id=DOID:2634 DOID:2634]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.035.320 C04.557.470.035.320]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.590.485 C04.557.470.590.485]

| Cystadenomas

| File:Pancreatic serous cystadenoma - high mag.jpg

|-

| cystathioninuria

| class of disease

| sulfuraminoacidemia
amino acid metabolic disorder
genetic disease

| amino acid metabolic disorder characterized by elevated plasma and urinary cystathionine levels that has material basis in homozygous or compound heterozygous mutation in the CTH gene on chromosome 1p31

| [http://www.disease-ontology.org/?id=DOID:0090142 DOID:0090142]

|

|

|

|-

| cystic basal cell carcinoma

| class of disease

| basal-cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4302 DOID:4302]

|

|

|

|-

| cystic echinococcosis

| class of disease

| echinococcosis
lung disease
bone disease
heart disease
liver disease
encephalopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1495 DOID:1495]

|

|

| File:Hydatid cyst.JPG

|-

| cystic kidney disease

| class of disease

| renal cyst
kidney disease

| congenital or acquired kidney disorder characterized by the presence of renal cysts

| [http://www.disease-ontology.org/?id=DOID:2975 DOID:2975]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.419.403 C12.777.419.403]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.419.403 C13.351.968.419.403]

| Cystic kidney diseases

|

|-

| cystic lymphangioma

| class of disease

| lymphangioma
Cystic lymphatic malformation
hygroma

| human disease

| [http://www.disease-ontology.org/?id=DOID:3081 DOID:3081]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.375.450.450 C04.557.375.450.450]

| Cystic hygroma

|

|-

| cystic nephroma

| class of disease

| kidney benign neoplasm
nephroma
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2673 DOID:2673]

|

| Cystic nephroma

|

|-

| cystic teratoma

| class of disease

| teratoma
benign teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2660 DOID:2660]

|

|

|

|-

| cystinuria

| class of disease

| amino acid metabolic disorder
ureteral disease
bladder disease
kidney disease
disease

| amino acid metabolic disorder that involves the formation of cystine stones in the kidneys, ureter, and bladder

| [http://www.disease-ontology.org/?id=DOID:9266 DOID:9266]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.419.815.885.250 C12.777.419.815.885.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.419.815.885.250 C13.351.968.419.815.885.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.861.885.250 C16.320.565.861.885.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.861.885.250 C18.452.648.861.885.250]

| Cystine crystals in urine

|

|-

| cystitis

| class of disease
symptom or sign

| bladder disease
inflammation
inflammatory disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1679 DOID:1679]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.777.829.495 C12.200.777.829.495]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.968.829.495 C12.050.351.968.829.495]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.950.829.495 C12.950.829.495]

| Cystitis

| File:Diverse e Coli.png

|-

| cystitis cystica

| class of disease

| cystitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:7138 DOID:7138]

|

| Cystitis cystica

|

|-

| cystoid macular edema

| class of disease

| macular retinal edema

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4447 DOID:4447]

|

|

|

|-

| cystoid macular retinal degeneration

| class of disease

| degeneration of macula and posterior pole

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14245 DOID:14245]

|

|

|

|-

| cytochrome P450 oxidoreductase deficiency

| class of disease

| steroid inherited metabolic disorder
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080925 DOID:0080925]

|

|

|

|-

| cytomegalovirus retinitis

| class of disease

| cytomegaloviral disease
retinitis
viral eye infection
disease

| retinitis that has material basis in Cytomegalovirus

| [http://www.disease-ontology.org/?id=DOID:0080160 DOID:0080160]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.375.725.270 C01.375.725.270]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.256.466.245.150 C01.925.256.466.245.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.294.800.270 C11.294.800.270]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.768.773.360 C11.768.773.360]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.325.270 C01.925.325.270]

| Cytomegalovirus retinitis

| File:Fundus photograph-CMV retinitis EDA07.JPG

|-

| dacryoadenitis

| class of disease

| lacrimal apparatus disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:950 DOID:950]

|

|

| File:Tear system.svg

|-

| dacryocystitis

| class of disease

| acute inflammation of lacrimal passage
disease

| infection of the lacrimal sac

| [http://www.disease-ontology.org/?id=DOID:9938 DOID:9938]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.496.221 C11.496.221]

| Dacryocystitis

|

|-

| dacryocystocele

| class of disease

| chronic inflammation of lacrimal passage

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9939 DOID:9939]

|

|

|

|-

| deafness, aminoglycoside-induced

| class of disease

| drug-induced hearing loss

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111734 DOID:0111734]

|

|

|

|-

| dedifferentiated liposarcoma

| class of disease

| liposarcoma

| liposarcoma that is characterized as a high-grade tumor that occurs when a lower-grade tumor changes and creates new high-grade cells

| [http://www.disease-ontology.org/?id=DOID:0080531 DOID:0080531]

|

|

|

|-

| deep angioma

| class of disease

| hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:469 DOID:469]

|

|

|

|-

| deep corneal vascularisation

| class of disease

| corneal neovascularization

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12087 DOID:12087]

|

|

|

|-

| deep keratitis

| class of disease

| keratitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:9858 DOID:9858]

|

|

|

|-

| deep leiomyoma

| class of disease

| leiomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5128 DOID:5128]

|

|

|

|-

| deficiency anemia

| class of disease

| anemia
nutritional deficiency disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13121 DOID:13121]

|

| Nutritional anemias

|

|-

| degeneration of macula and posterior pole

| class of disease

| macular degeneration

| human disease

| [http://www.disease-ontology.org/?id=DOID:2007 DOID:2007]

|

|

|

|-

| degenerative disc disease

| class of disease

| Intervertebral disc disorder
bone deterioration disease

| bone deterioration disease that has material basis in gradual dehydration and tears located in intervertebral disc

| [http://www.disease-ontology.org/?id=DOID:90 DOID:90]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.900.153 C05.116.900.153]

| Degenerative disc disease

| File:Cervical Spine MRI showing degenerative changes closeup.jpg

|-

| degenerative myopia

| class of disease

| eye degenerative disease
myopia

| Excessive axial myopia associated with complications (especially posterior staphyloma and choroidal neovascularization) that can lead to blindness

| [http://www.disease-ontology.org/?id=DOID:11829 DOID:11829]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.744.636.500 C11.744.636.500]

|

|

|-

| dehydrated hereditary stomatocytosis

| class of disease

| hereditary stomatocytosis
hemolytic anemia

|

| [http://www.disease-ontology.org/?id=DOID:0111575 DOID:0111575]

|

|

|

|-

| dehydrated hereditary stomatocytosis 1

| class of disease

| dehydrated hereditary stomatocytosis
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111576 DOID:0111576]

|

|

|

|-

| dehydration polycythemia

| class of disease

| acquired polycythemia
hemoconcentration

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2833 DOID:2833]

|

|

|

|-

| delayed sleep phase disorder

| class of disease

| sleep disorder
circadian rhythm sleep disorder
disease

| chronic mismatch between a person's normal daily rhythm, compared to other people and societal norms

| [http://www.disease-ontology.org/?id=DOID:0111141 DOID:0111141]

|

|

|

|-

| delta chain disease

| class of disease

| heavy chain disease

| heavy chain disease that results from an overproduction of delta antibody (IgD)

| [http://www.disease-ontology.org/?id=DOID:0060129 DOID:0060129]

|

|

|

|-

| delta thalassemia

| class of disease

| thalassemia
beta thalassemia
autosomal dominant disease

| type of thalassemia

| [http://www.disease-ontology.org/?id=DOID:0080773 DOID:0080773]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.141.150.875.575 C15.378.071.141.150.875.575]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.420.826.200 C15.378.420.826.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.070.875.575 C16.320.070.875.575]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.365.826.575 C16.320.365.826.575]

|

|

|-

| delusional disorder

| class of disease
symptom or sign

| psychosis
disease

| mental disease

| [http://www.disease-ontology.org/?id=DOID:778 DOID:778]

|

|

|

|-

| dementia

| class of disease
symptom or sign

| cognitive disorder
organic brain syndrome
clinical sign
disability affecting intellectual abilities
disease

| long-term brain disorder causing personality changes and impaired memory, reasoning, and social function

| [http://www.disease-ontology.org/?id=DOID:1307 DOID:1307]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.380 C10.228.140.380]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.615.400 F03.615.400]

| Dementia

| File:An old man diagnosed as suffering from senile dementia. Colo Wellcome L0026689.jpg

|-

| demyelinating disease

| class of disease

| neurological disorder
neurodegeneration
central nervous system disease
disease

| type of neurological disease where the myelin sheath of neurons is damaged

| [http://www.disease-ontology.org/?id=DOID:3213 DOID:3213]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.314 C10.314]

| Demyelinating diseases

| File:MS Demyelinisation CD68 10xv2.jpg

|-

| demyelinating polyneuropathy

| class of disease

| polyneuropathy
spinal cord disease
demyelinating disease

| Polyneuropathy that is characterized by demyelination of axons

| [http://www.disease-ontology.org/?id=DOID:5214 DOID:5214]

|

|

|

|-

| dendritic cell deficiency

| class of disease

| primary immunodeficiency disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111963 DOID:0111963]

|

|

|

|-

| dendritic cell sarcoma

| class of disease

| histiocytic and dendritic cell cancer
sarcoma
dendritic cell tumor

| histiocytic and dendritic cell cancer that is mainly located in lymph nodes

| [http://www.disease-ontology.org/?id=DOID:7849 DOID:7849]

|

|

|

|-

| dendritic cell thymoma

| class of disease

| thymoma
leukocyte disease
hematologic cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3282 DOID:3282]

|

|

|

|-

| dengue shock syndrome

| class of disease

| dengue fever
dengue hemorrhagic fever

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050125 DOID:0050125]

|

|

|

|-

| dental abscess

| class of disease
symptom or sign

| tooth pathology
abscess

| tooth disease characterized by a localized collection of pus associated with a tooth

| [http://www.disease-ontology.org/?id=DOID:0060324 DOID:0060324]

|

| Tooth abscess

| File:Abces parulique.jpg

|-

| dental caries

| class of disease

| teeth hard tissue disease
caries

| deformation of teeth made by acids from bacteria

| [http://www.disease-ontology.org/?id=DOID:216 DOID:216]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.793.720.210 C07.793.720.210]

| Dental caries

| File:Tooth model.jpg

|-

| dental enamel hypoplasia

| class of disease

| teeth hard tissue disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:693 DOID:693]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.650.800.255 C07.650.800.255]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.793.700.255 C07.793.700.255]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.850.800.255 C16.131.850.800.255]

| Enamel hypoplasia

| File:법랑질저형성증.jpg

|-

| dental fluorosis

| class of disease

| tooth pathology
fluoride toxicity
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:13711 DOID:13711]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.793.330 C07.793.330]

| Dental fluorosis

| File:Dental Flurosis (teeth with brown stains).jpg

|-

| dental pulp calcification

| class of disease

| dental pulp disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5608 DOID:5608]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.793.237.252 C07.793.237.252]

|

|

|-

| dental pulp disease

| class of disease

| tooth pathology
connective tissue disease

| disease involving the dental pulp

| [http://www.disease-ontology.org/?id=DOID:5330 DOID:5330]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.793.237 C07.793.237]

|

|

|-

| dental pulp necrosis

| class of disease

| dental pulp disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11623 DOID:11623]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.793.237.315 C07.793.237.315]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.717.182 C23.550.717.182]

|

|

|-

| dentin caries

| class of disease

| dental caries

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10461 DOID:10461]

|

|

|

|-

| dentine erosion

| class of disease

| dental erosion

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13629 DOID:13629]

|

|

|

|-

| dentine hypersensitivity

| class of disease

| orofacial pain
teeth hard tissue disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:698 DOID:698]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.793.266 C07.793.266]

|

|

|-

| denture stomatitis

| class of disease

| stomatitis

| lip disease

| [http://www.disease-ontology.org/?id=DOID:11875 DOID:11875]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.864.875 C07.465.864.875]

|

|

|-

| dependent personality disorder

| class of disease

| personality disorder
dependency
disease

| personality disorder that is characterized by a pervasive psychological dependence on other people

| [http://www.disease-ontology.org/?id=DOID:10931 DOID:10931]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.675.200 F03.675.200]

| Dependent personality disorder

|

|-

| depersonalization disorder

| class of disease

| dissociative disorder
depersonalization

| dissociative disorder in which the sufferer is affected by persistent or recurrent feelings of depersonalization and/or derealization

| [http://www.disease-ontology.org/?id=DOID:11038 DOID:11038]

|

|

|

|-

| dermal unilateral segmental cavernous angioma

| class of disease

| cavernous hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3148 DOID:3148]

|

|

|

|-

| dermatitis

| class of disease
symptom or sign

| skin disease
skin and integumentary tissue symptom
disease

| inflammation of the skin

| [http://www.disease-ontology.org/?id=DOID:2723 DOID:2723]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.174 C17.800.174]

| Dermatitis

| File:Dermatitis2015.jpg

|-

| dermatitis herpetiformis

| class of disease
symptom or sign

| autoimmune skin disease
bullous skin disease
pemphigoid
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:8505 DOID:8505]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.174.360 C17.800.174.360]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.865.360 C17.800.865.360]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.318 C20.111.318]

| Dermatitis herpetiformis

|

|-

| dermatographia

| class of disease

| physical urticaria
disease

| human skin condition, responsible for "skin writing" effect in those affected

| [http://www.disease-ontology.org/?id=DOID:743 DOID:743]

|

| Dermatographic urticaria

| File:Dermographism in child.jpg

|-

| dermatomycosis

| class of disease

| skin disease
fungal infectious disease
skin infection

| cutaneous mycosis that results in fungal infection located in skin or of its appendages, has material basis in Ascomycota fungi other than the dermatophytes

| [http://www.disease-ontology.org/?id=DOID:1563 DOID:1563]
[http://www.disease-ontology.org/?id=DOID:0050134 DOID:0050134]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.703.302 C01.150.703.302]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.800.200 C01.800.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.838.208 C17.800.838.208]

|

|

|-

| dermatosis papulosa nigra

| class of disease

| dermatitis
seborrheic keratosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4400 DOID:4400]

|

| Dermatosis papulosa nigra

|

|-

| dermis tumor

| class of disease

| skin benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2438 DOID:2438]

|

|

|

|-

| dermoid cyst

| class of disease

| cystic teratoma
disease

| tissue disease

| [http://www.disease-ontology.org/?id=DOID:2658 DOID:2658]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.182.201 C04.182.201]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.910.250 C04.557.465.910.250]

| Dermoid cysts

| File:Dermoid cyst intracranial.jpg

|-

| dermoid cyst of ovary

| class of disease

| ovarian cyst
ovarian cancer
dermoid cyst
ovarian benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5117 DOID:5117]

|

| Ovarian dermoid cysts

|

|-

| dermoid cyst of skin

| class of disease

| skin cancer
skin benign neoplasm
dermoid cyst

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13691 DOID:13691]

|

|

|

|-

| descending colon cancer

| class of disease

| plump cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12190 DOID:12190]

|

|

|

|-

| desmoid disease, hereditary

| class of disease

| aggressive fibromatosis
syndrome
autosomal genetic disease

| desmoid tumor (DT) is a benign, locally invasive soft tissue tumor associated with a high recurrence rate but with no metastatic potential

| [http://www.disease-ontology.org/?id=DOID:0111349 DOID:0111349]

|

|

|

|-

| desmoplastic small-round-cell tumor

| class of disease

| soft-tissue sarcoma
sarcoma

| aggressive, rare cancer

| [http://www.disease-ontology.org/?id=DOID:6785 DOID:6785]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.315 C04.557.450.795.315]

| Desmoplastic small round cell tumour

|

|-

| detrusor sphincter dyssynergia

| class of disease

| neurogenic bladder
bladder disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12145 DOID:12145]

|

|

|

|-

| deuteranopia

| class of disease

| congenital color blindness
color blindness
red–green color blindness
dichromatopsia

| human disease, green color blindness

| [http://www.disease-ontology.org/?id=DOID:13909 DOID:13909]

|

| Deuteranopia

|

|-

| developmental and epileptic encephalopathy

| class of disease

| electroclinical syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112202 DOID:0112202]

|

|

|

|-

| developmental and epileptic encephalopathy 100

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070386 DOID:0070386]

|

|

|

|-

| developmental and epileptic encephalopathy 101

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070387 DOID:0070387]

|

|

|

|-

| developmental and epileptic encephalopathy 102

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070388 DOID:0070388]

|

|

|

|-

| developmental and epileptic encephalopathy 103

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070389 DOID:0070389]

|

|

|

|-

| developmental and epileptic encephalopathy 104

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070390 DOID:0070390]

|

|

|

|-

| developmental and epileptic encephalopathy 108

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070394 DOID:0070394]

|

|

|

|-

| developmental and epileptic encephalopathy 109

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070378 DOID:0070378]

|

|

|

|-

| developmental and epileptic encephalopathy 110

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070395 DOID:0070395]

|

|

|

|-

| developmental and epileptic encephalopathy 67

| class of disease

| developmental and epileptic encephalopathy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112203 DOID:0112203]

|

|

|

|-

| developmental and epileptic encephalopathy 68

| class of disease

| autosomal recessive disease
developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112204 DOID:0112204]

|

|

|

|-

| developmental and epileptic encephalopathy 69

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112205 DOID:0112205]

|

|

|

|-

| developmental and epileptic encephalopathy 70

| class of disease

| autosomal dominant disease
developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112206 DOID:0112206]

|

|

|

|-

| developmental and epileptic encephalopathy 71

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112207 DOID:0112207]

|

|

|

|-

| developmental and epileptic encephalopathy 72

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112208 DOID:0112208]

|

|

|

|-

| developmental and epileptic encephalopathy 73

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112209 DOID:0112209]

|

|

|

|-

| developmental and epileptic encephalopathy 74

| class of disease

| developmental and epileptic encephalopathy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112210 DOID:0112210]

|

|

|

|-

| developmental and epileptic encephalopathy 75

| class of disease

| developmental and epileptic encephalopathy
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112211 DOID:0112211]

|

|

|

|-

| developmental and epileptic encephalopathy 78

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112214 DOID:0112214]

|

|

|

|-

| developmental and epileptic encephalopathy 79

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112215 DOID:0112215]

|

|

|

|-

| developmental and epileptic encephalopathy 80

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112216 DOID:0112216]

|

|

|

|-

| developmental and epileptic encephalopathy 81

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112217 DOID:0112217]

|

|

|

|-

| developmental and epileptic encephalopathy 83

| class of disease

| autosomal recessive disease
developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112218 DOID:0112218]

|

|

|

|-

| developmental and epileptic encephalopathy 84

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112219 DOID:0112219]

|

|

|

|-

| developmental and epileptic encephalopathy 89

| class of disease

| developmental and epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112223 DOID:0112223]

|

|

|

|-

| developmental coordination disorder

| class of disease

| motor disorder
specific developmental disorder
disease

| neurodevelopmental condition

| [http://www.disease-ontology.org/?id=DOID:9923 DOID:9923]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.625.813 F03.625.813]

| Dyspraxia

|

|-

| developmental delay and seizures with or without movement abnormalities

| class of disease

| syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080473 DOID:0080473]

|

|

|

|-

| developmental disorder

| class of disease

| mental disorder
developmental disability
neurodevelopmental disorder
disease

| disease of mental health that occur during a child's developmental period between birth and age 18 resulting in retarding of the child's psychological or physical development

| [http://www.disease-ontology.org/?id=DOID:0060037 DOID:0060037]

|

|

|

|-

| dextro-looped transposition of the great arteries 1

| class of disease

| dextro-transposition of the great arteries
genetic disease
autosomal dominant disease

| dextro-looped transposition of the great arteries that has material basis in heterozygous missense mutation in the MED13L gene on chromosome 12q24

| [http://www.disease-ontology.org/?id=DOID:0060771 DOID:0060771]

|

|

|

|-

| dextrocardia

| class of disease

| heart position anomaly
congenital heart disease
disease

| rare congenital defect in which the apex of the heart is located on the right side of the body

| [http://www.disease-ontology.org/?id=DOID:9565 DOID:9565]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.240.400.280 C14.240.400.280]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.400.280 C14.280.400.280]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.240.400.280 C16.131.240.400.280]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.810.250 C16.131.810.250]

| Dextrocardia

| File:Situs inversus chest Nevit.jpg

|-

| diabetes

| class of disease

| glucose metabolism disease
disease

| group of metabolic disorders characterized by high blood sugar levels over a prolonged period

| [http://www.disease-ontology.org/?id=DOID:9351 DOID:9351]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.394.750 C18.452.394.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.246 C19.246]

| Diabetes mellitus

| File:Blue circle for diabetes.svg

|-

| diabetes

| class of disease

| glucose metabolism disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0081062 DOID:0081062]

|

|

|

|-

| diabetic angiopathy

| class of disease

| peripheral vascular disease
complications of diabetes mellitus

| human disease

| [http://www.disease-ontology.org/?id=DOID:11713 DOID:11713]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.320 C14.907.320]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.246.099.500 C19.246.099.500]

| Diabetic angiopathy

|

|-

| diabetic autonomic neuropathy

| class of disease

| autonomic neuropathy
diabetic neuropathy

| Autonomic neuropathy that is caused by diabetes mellitus

| [http://www.disease-ontology.org/?id=DOID:11503 DOID:11503]

|

|

|

|-

| diabetic cataract

| class of disease

| cataract
ocular manifestation of diabetes

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13328 DOID:13328]

|

|

|

|-

| diabetic encephalopathy

| class of disease

| encephalopathy
complications of diabetes mellitus

| brain disease that is characterized by functional impairment of cognition, cerebral signal conduction, neurotransmission and synaptic plasticity, and underlying structural pathology associated with diabetes

| [http://www.disease-ontology.org/?id=DOID:0050850 DOID:0050850]

|

|

|

|-

| diabetic ketoacidosis

| class of disease

| complications of diabetes mellitus
type 2 diabetes
ketoacidosis
metabolic acidosis
disease

| potentially life-threatening complication in people with diabetes mellitus

| [http://www.disease-ontology.org/?id=DOID:1837 DOID:1837]
[http://www.disease-ontology.org/?id=DOID:10626 DOID:10626]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.076.176.652.500 C18.452.076.176.652.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.394.750.535 C18.452.394.750.535]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.246.099.812 C19.246.099.812]

| Diabetic ketoacidosis

| File:Infuuszakjes.jpg

|-

| diabetic macular edema

| class of disease

| macular retinal edema
diabetic retinopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9191 DOID:9191]

|

| Diabetic macular edema

|

|-

| diabetic neuropathy

| class of disease

| complications of diabetes mellitus
peripheral neuropathy
disease

| neurological complication of persistently high blood sugar

| [http://www.disease-ontology.org/?id=DOID:9743 DOID:9743]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.300 C10.668.829.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.246.099.937 C19.246.099.937]

| Diabetic neuropathy

| File:Diapason.jpg

|-

| diabetic polyneuropathy

| class of disease

| diabetic neuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12785 DOID:12785]

|

|

|

|-

| diabetic retinopathy

| class of disease

| ocular manifestation of diabetes
diabetic angiopathy
retinal vascular disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:8947 DOID:8947]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.768.257 C11.768.257]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.320.382 C14.907.320.382]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.246.099.500.382 C19.246.099.500.382]

| Diabetic retinopathy

| File:Human eyesight two children and ball normal vision.jpg

|-

| diaphragm disease

| class of disease

| muscular disease
respiratory disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:10481 DOID:10481]

|

| Disorders of diaphragm

|

|-

| diaphragmatic eventration

| class of disease

| diaphragm disease

| congenital or acquired abnormality characterized by elevation of the hemidiaphragm

| [http://www.disease-ontology.org/?id=DOID:10480 DOID:10480]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.198.257 C06.198.257]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.314.244 C16.131.314.244]

|

|

|-

| diarrhea

| class of disease
symptom or sign

| gastrointestinal system disease
clinical sign
feces and droppings symptom
disease

| loose or liquid bowel movements

| [http://www.disease-ontology.org/?id=DOID:13250 DOID:13250]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.821.214 C23.888.821.214]

| Diarrhea

| File:Multiple rotavirus particles.jpg

|-

| diclofenac allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger diclofenac

| [http://www.disease-ontology.org/?id=DOID:0040031 DOID:0040031]

|

|

|

|-

| diencephalic astrocytoma

| class of disease

| diencephalic neoplasm
brain glioma
brain astrocytoma
glioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4855 DOID:4855]

|

|

|

|-

| diencephalic neoplasm

| class of disease

| supratentorial cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:3843 DOID:3843]

|

|

|

|-

| differentiated thyroid carcinoma

| class of disease

| thyroid carcinoma
thyroid gland adenocarcinoma

| Differentiated thyroid carcinoma (DTC), also known as papillary or follicular thyroid carcinoma, is a slow-growing malignancy usually presenting in adults as an asymptomatic thyroid mass

| [http://www.disease-ontology.org/?id=DOID:0080525 DOID:0080525]

|

|

|

|-

| differentiating neuroblastoma

| class of disease

| neuroblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4160 DOID:4160]

|

|

|

|-

| diffuse alopecia areata

| class of disease

| alopecia areata

| alopecia areata that involves diffuse loss of hair over the whole scalp

| [http://www.disease-ontology.org/?id=DOID:0060157 DOID:0060157]

|

|

|

|-

| diffuse cutaneous mastocytosis

| class of disease

| cutaneous mastocytosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3665 DOID:3665]

|

|

|

|-

| diffuse cystic renal dysplasia

| class of disease

| cystic kidney disease
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111682 DOID:0111682]

|

|

|

|-

| diffuse gastric cancer

| class of disease

| stomach cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080763 DOID:0080763]

|

|

|

|-

| diffuse glomerulonephritis

| class of disease

| glomerulonephritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4781 DOID:4781]

|

|

|

|-

| diffuse infiltrative lymphocytosis syndrome

| class of disease

| syndrome
lymphocytosis
AIDS related disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6677 DOID:6677]

|

|

|

|-

| diffuse interstitial keratitis

| class of disease

| interstitial keratitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13353 DOID:13353]

|

|

|

|-

| diffuse large B-cell lymphoma

| class of disease

| B-cell lymphoma
aggressive B-cell non-Hodgkin lymphoma

| type of lymphoma (cancer)

| [http://www.disease-ontology.org/?id=DOID:0050745 DOID:0050745]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386.480.150.585 C04.557.386.480.150.585]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.569.480.150.585 C15.604.515.569.480.150.585]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.761.480.150.585 C20.683.515.761.480.150.585]

| Diffuse large B-cell lymphoma

| File:Diffuse large B cell lymphoma - cytology low mag.jpg

|-

| diffuse lipomatosis

| class of disease

| lipomatosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3923 DOID:3923]

|

|

|

|-

| diffuse meningeal melanocytosis

| class of disease

| central nervous system melanocytic neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6379 DOID:6379]

|

|

|

|-

| diffuse midline glioma, H3 K27M-mutant

| class of disease

| glioma
juvenile astrocytoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080684 DOID:0080684]

|

|

|

|-

| diffuse peritoneal leiomyomatosis

| class of disease

| leiomyomatosis
primary peritoneal tumor
leiomyoma
peritoneal benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5728 DOID:5728]

|

|

|

|-

| diffuse pulmonary fibrosis

| class of disease

| pulmonary fibrosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:5641 DOID:5641]

|

|

|

|-

| diffuse scleroderma

| class of disease

| systemic scleroderma

| variant of systemic scleroderma characterized by sclerosis of the skin, Raynaud phenomenon, and organ involvement, including pulmonary fibrosis, renal disease, and gastrointestinal tract involvement

| [http://www.disease-ontology.org/?id=DOID:1580 DOID:1580]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.799.602 C17.300.799.602]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.784.602 C17.800.784.602]

|

|

|-

| diffuse secondary choroid atrophy

| class of disease

| choroidal sclerosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:981 DOID:981]

|

|

|

|-

| diffuse uterine leiomyomatosis

| class of disease

| uterine fibroid
uterine corpus leiomyomatosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5917 DOID:5917]

|

|

|

|-

| digenic disease

| class of disease

| polygenic disease

| polygenic disease that is characterized by expression of a phenotype that requires the presence of pathogenic variants in two different genes

| [http://www.disease-ontology.org/?id=DOID:0080578 DOID:0080578]

|

|

|

|-

| dihydropyrimidinase deficiency

| class of disease

| pyrimidine metabolic disorder
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111629 DOID:0111629]

|

|

|

|-

| dilated cardiomyopathy 1A

| class of disease

| dilated cardiomyopathy
genetic disease

| dilated cardiomyopathy that has material basis in mutation in the LMNA gene on chromosome 1q21

| [http://www.disease-ontology.org/?id=DOID:0110425 DOID:0110425]

|

|

|

|-

| dilated cardiomyopathy 1B

| class of disease

| dilated cardiomyopathy
genetic disease

| dilated cardiomyopathy that has material basis in variation in the chromosome region 9q13

| [http://www.disease-ontology.org/?id=DOID:0110443 DOID:0110443]

|

|

|

|-

| dilated cardiomyopathy 1H

| class of disease

| dilated cardiomyopathy
genetic disease
monogenic disease

| dilated cardiomyopathy that has material basis in variation in the chromosome region 2q14-q22

| [http://www.disease-ontology.org/?id=DOID:0110429 DOID:0110429]

|

|

|

|-

| dilated cardiomyopathy 1K

| class of disease

| dilated cardiomyopathy
genetic disease
monogenic disease

| dilated cardiomyopathy that has material basis in variation in the chromosome region 6q12-q16

| [http://www.disease-ontology.org/?id=DOID:0110437 DOID:0110437]

|

|

|

|-

| dilated cardiomyopathy 1KK

| class of disease

| dilated cardiomyopathy
genetic disease
autosomal dominant disease

| dilated cardiomyopathy that has material basis in mutation in the MYPN gene on chromosome 10q21

| [http://www.disease-ontology.org/?id=DOID:0110445 DOID:0110445]

|

|

|

|-

| dilated cardiomyopathy 1Q

| class of disease

| dilated cardiomyopathy
genetic disease
monogenic disease

| A dilated cardiomyopathy that has material basis in variation in the chromosome region 7q22.3-q31.1.

| [http://www.disease-ontology.org/?id=DOID:0110442 DOID:0110442]

|

|

|

|-

| dioctophymiasis

| class of disease

| parasitic helminthiasis infectious disease
kidney disease
skin disease

| A parasitic helminthiasis infectious disease that involves parasitic infection by the nematode Dioctophyme renale in humans after eating undercooked food. The larvae are found in the subcutaneous nodules and kidneys.

| [http://www.disease-ontology.org/?id=DOID:0050260 DOID:0050260]

|

|

|

|-

| diphenylmethane-4,4'-diisocyanate allergic asthma

| class of disease

| isocyanates allergic asthma

| allergic asthma to isocyanates that has allergic trigger diphenylmethane-4,4-diisocyanate

| [http://www.disease-ontology.org/?id=DOID:0040042 DOID:0040042]

|

|

|

|-

| diphenylmethane-4,4'-diisocyanate allergic contact dermatitis

| class of disease

| allergic contact dermatitis

| allergic contact dermatitis that has allergic trigger diphenylmethane-4,4-diisocyanate

| [http://www.disease-ontology.org/?id=DOID:0040052 DOID:0040052]

|

|

|

|-

| diphtheritic cystitis

| class of disease

| cystitis
diphtheria

| cystitis which involves inflammation and formation of a dense fibrous false membrane on the mucous membrane of the bladder

| [http://www.disease-ontology.org/?id=DOID:13306 DOID:13306]

|

|

|

|-

| diphtheritic peritonitis

| class of disease

| peritonitis
diphtheria

| peritonitis which involves inflammation of peritoneal cavity by Corynebacterium diphtheriae

| [http://www.disease-ontology.org/?id=DOID:13310 DOID:13310]

|

|

|

|-

| diplegia of upper limb

| class of disease

| neurological disorder
Diplegia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:862 DOID:862]

|

|

|

|-

| discharging ear

| class of disease
symptom or sign

| ear disease
discharge

| human disease

| [http://www.disease-ontology.org/?id=DOID:10261 DOID:10261]

|

|

|

|-

| discoid lupus erythematosus of eyelid

| class of disease

| discoid lupus erythematosus
noninfectious dermatoses of eyelid

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9076 DOID:9076]

|

|

|

|-

| discrete subaortic stenosis

| class of disease

| subvalvular aortic stenosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5804 DOID:5804]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.484.150.070.210 C14.280.484.150.070.210]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.955.249.070.210 C14.280.955.249.070.210]

|

|

|-

| disease

| class of disease

| health problem
biological process

| abnormal condition negatively affecting organisms

| [http://www.disease-ontology.org/?id=DOID:4 DOID:4]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.288 C23.550.288]

| Diseases and disorders

| File:Gabriel von Max Die ekstatische Jungfrau Katharina Emmerich.jpg

|-

| disease of anatomical entity

| class of disease

| disease

| disease that manifests in a defined anatomical structure

| [http://www.disease-ontology.org/?id=DOID:7 DOID:7]

|

|

|

|-

| disease of cellular proliferation

| class of disease

| disease

| disease characterized by abnormally rapid cell division

| [http://www.disease-ontology.org/?id=DOID:14566 DOID:14566]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.697 C04.697]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.727 C23.550.727]

|

|

|-

| dislocation of ear ossicle

| class of disease

| middle ear disease
conductive hearing loss
ear disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11129 DOID:11129]

|

|

|

|-

| disodium cromoglycate allergy

| class of disease

| drug allergy
metal allergy

| drug allergy that has allergic trigger disodium cromoglycate

| [http://www.disease-ontology.org/?id=DOID:0040073 DOID:0040073]

|

|

|

|-

| displacement of cardia through esophageal hiatus

| class of disease

| hiatus hernia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12641 DOID:12641]

|

|

|

|-

| disseminated chorioretinitis

| class of disease

| chorioretinitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8787 DOID:8787]

|

|

|

|-

| disseminated eosinophilic collagen disease

| class of disease

| collagen disease
eosinophilia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9499 DOID:9499]

|

|

|

|-

| disseminated intravascular coagulation

| class of disease

| thrombophilia
disease

| pathological process characterized by the widespread activation of the clotting cascade that results in the formation of blood clots in the small blood vessels throughout the body

| [http://www.disease-ontology.org/?id=DOID:11247 DOID:11247]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100.220 C15.378.100.220]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463.250 C15.378.463.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.925.220 C15.378.925.220]

| Disseminated intravascular coagulation

| File:DIC With Microangiopathic Hemolytic Anemia.jpg

|-

| disseminated superficial actinic porokeratosis

| class of disease

| keratosis
porokeratosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3805 DOID:3805]

|

|

|

|-

| dissociated nystagmus

| class of disease

| pathologic nystagmus

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13174 DOID:13174]

|

|

|

|-

| dissociative amnesia

| class of disease

| dissociative disorder
amnesia
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11037 DOID:11037]

|

| Dissociative amnesia

|

|-

| dissociative disorder

| class of disease

| mental disorder
dissociation
disease

| disease of mental health in which the normally well-integrated functions of memory, identity, perception, or consciousness are separated (dissociated)

| [http://www.disease-ontology.org/?id=DOID:10935 DOID:10935]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.300 F03.300]

|

|

|-

| distal arthrogryposis type 1

| class of disease

| distal arthrogryposis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111596 DOID:0111596]

|

|

|

|-

| distal arthrogryposis type 10

| class of disease

| autosomal dominant disease
distal arthrogryposis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111593 DOID:0111593]

|

|

|

|-

| distal arthrogryposis type 1A

| class of disease

| autosomal dominant disease
distal arthrogryposis type 1

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111597 DOID:0111597]

|

|

|

|-

| distal arthrogryposis type 1B

| class of disease

| distal arthrogryposis type 1
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111598 DOID:0111598]

|

|

|

|-

| distal arthrogryposis type 2A

| class of disease

| Freeman–Sheldon syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111605 DOID:0111605]

|

|

|

|-

| distal arthrogryposis type 2B1

| class of disease

| autosomal dominant disease
Sheldon-Hall syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111600 DOID:0111600]

|

|

|

|-

| distal arthrogryposis type 2B2

| class of disease

| Sheldon-Hall syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111601 DOID:0111601]

|

|

|

|-

| distal arthrogryposis type 2B3

| class of disease

| Sheldon-Hall syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111602 DOID:0111602]

|

|

|

|-

| distal arthrogryposis type 3

| class of disease

| autosomal dominant disease
distal arthrogryposis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111607 DOID:0111607]

|

|

|

|-

| distal arthrogryposis type 4

| class of disease

| distal arthrogryposis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111610 DOID:0111610]

|

|

|

|-

| distal arthrogryposis type 5

| class of disease

| autosomal dominant disease
distal arthrogryposis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111608 DOID:0111608]

|

|

|

|-

| distal arthrogryposis type 5D

| class of disease

| distal arthrogryposis
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111594 DOID:0111594]

|

|

|

|-

| distal arthrogryposis type 6

| class of disease

| distal arthrogryposis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111609 DOID:0111609]

|

|

|

|-

| distal biliary tract carcinoma

| class of disease

| bile duct carcinoma
extrahepatic bile duct carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5923 DOID:5923]

|

|

|

|-

| distal hereditary motor neuronopathy type 2

| class of disease

|

| autosomal dominant distal hereditary motor neuronopathy characterized by adult onset of slowly progressive distal atrophy and weakness

| [http://www.disease-ontology.org/?id=DOID:0111206 DOID:0111206]

|

|

|

|-

| distal hereditary motor neuronopathy type 2A

| class of disease

| distal hereditary motor neuronopathy type 2

| A distal hereditary motor neuropathy type 2 that has material basis in heterozygous mutation in HSPB8 on 12q24.23.

| [http://www.disease-ontology.org/?id=DOID:0111208 DOID:0111208]

|

|

|

|-

| distal hereditary motor neuronopathy type 5

| class of disease

| autosomal dominant distal hereditary motor neuropathy

| autosomal dominant distal hereditary motor neuronopathy characterized by muscle weakness and wasting, predominantly confined to the hands, and often exclusively involve thenar and/or interosseus dorsalis I eminences

| [http://www.disease-ontology.org/?id=DOID:0111203 DOID:0111203]

|

|

|

|-

| distal hereditary motor neuronopathy type 5A

| class of disease

| distal hereditary motor neuronopathy type 5

| A distal hereditary motor neuronopathy type 5 that has material basis in heterozygous mutation in GARS on 7p14.3 or BSCL2 on 11q12.3.

| [http://www.disease-ontology.org/?id=DOID:0111204 DOID:0111204]

|

|

|

|-

| distal hereditary motor neuronopathy type 7

| class of disease

| autosomal dominant distal hereditary motor neuropathy

| autosomal dominant distal hereditary motor neuronopathy characterized by slowly progressive distal atrophy and weakness affecting first the upper limbs and later the lower limbs and vocal cord paresis

| [http://www.disease-ontology.org/?id=DOID:0111199 DOID:0111199]

|

|

|

|-

| distal hereditary motor neuronopathy type 7A

| class of disease

| distal hereditary motor neuronopathy type 7

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111201 DOID:0111201]

|

|

|

|-

| distal hereditary motor neuronopathy type 7B

| class of disease

| distal hereditary motor neuronopathy type 7

| A distal hereditary motor neuropathy type 7 that has material basis in heterozygous mutation in DCTN1 on 2p13.1.

| [http://www.disease-ontology.org/?id=DOID:0111202 DOID:0111202]

|

|

|

|-

| distal hereditary motor neuronopathy type 8

| class of disease

| autosomal dominant distal hereditary motor neuropathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111215 DOID:0111215]

|

|

|

|-

| distal hereditary motor neuronopathy type 9

| class of disease

| autosomal dominant distal hereditary motor neuropathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111212 DOID:0111212]

|

|

|

|-

| distal hereditary motor neuropathy type 1

| class of disease

| nervous system heredodegenerative disease
autosomal dominant distal hereditary motor neuropathy

| autosomal dominant neurodegenerative disorder characterized by juvenile onset, distal motor weakness without sensory impairment, and anterior horn cell degeneration

| [http://www.disease-ontology.org/?id=DOID:0111200 DOID:0111200]

|

|

|

|-

| distal hereditary motor neuropathy type 2B

| class of disease

| distal hereditary motor neuronopathy type 2

| A distal hereditary motor neuropathy type 2 that has material basis in heterozygous mutation in HSPB1 on 7q11.23.

| [http://www.disease-ontology.org/?id=DOID:0111207 DOID:0111207]

|

|

|

|-

| distal muscular dystrophy 3

| class of disease

|

| distal muscular dystrophy that has significant linkage to 2 distinct regions on chromosomes 8p22-q11 and 12q13-q22

| [http://www.disease-ontology.org/?id=DOID:0111189 DOID:0111189]

|

|

|

|-

| distal myopathy 1

| class of disease

| distal muscular dystrophy
genetic disease
autosomal dominant disease

| distal muscular dystrophy characterized by autosomal dominant inheritance that has material basis in mutation in the MYH7 gene on chromosome 14q11

| [http://www.disease-ontology.org/?id=DOID:0070197 DOID:0070197]

|

|

|

|-

| distal spinal muscular atrophy type 3

| class of disease

| nervous system heredodegenerative disease
autosomal recessive distal hereditary motor neuropathy
autosomal recessive distal hereditary motor neuronopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111211 DOID:0111211]

|

|

|

|-

| distal spinal muscular atrophy type 4

| class of disease

| autosomal recessive distal hereditary motor neuronopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111213 DOID:0111213]

|

|

|

|-

| distal spinal muscular atrophy type 5

| class of disease

| autosomal recessive distal hereditary motor neuronopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111214 DOID:0111214]

|

|

|

|-

| disuse amblyopia

| class of disease

| amblyopia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10378 DOID:10378]

|

|

|

|-

| diversion colitis

| class of disease

| colitis

| colitis caused by diversion of the fecal stream due to complication of ileostomy or colostomy

| [http://www.disease-ontology.org/?id=DOID:0060187 DOID:0060187]

|

|

|

|-

| diverticulitis

| class of disease
symptom or sign

| intestinal disease
diverticular disease
inflammatory disease
sigmoiditis
disease

| digestive disease caused by an inflammation of a herniating pouch (diverticulum) within the wall of the intestine, most often colon

| [http://www.disease-ontology.org/?id=DOID:7475 DOID:7475]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.539.463.199.375 C01.539.463.199.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.282.500 C06.405.205.282.500]

| Diverticulitis

| File:Diverticula, sigmoid colon.jpg

|-

| diverticulitis of colon

| class of disease

| colonic disease
diverticulitis
colonic diverticulosis

| colonic disease characterized by the formation and inflammation of diverticula within the colon wall

| [http://www.disease-ontology.org/?id=DOID:13254 DOID:13254]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.158.587.500 C06.405.469.158.587.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.539.463.199.375.250 C01.539.463.199.375.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.282.500.250 C06.405.205.282.500.250]

|

|

|-

| dominant beta-thalassemia

| class of disease

| beta thalassemia
autosomal dominant disease

| Dominant beta-thalassemia is a form of beta-thalassemia (see this term) resulting in moderate to severe anemia

| [http://www.disease-ontology.org/?id=DOID:0080770 DOID:0080770]

|

|

|

|-

| dominant dystrophic epidermolysis bullosa

| class of disease

| epidermolysis bullosa dystrophica
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080224 DOID:0080224]

|

|

|

|-

| dominant pericentral pigmentary retinopathy

| class of disease

| retinitis pigmentosa
autosomal dominant disease

| retinitis pigmentosa that is characterized pigmentary retinal degeneration with onset in the teens leading to blindness in the sixth ans seventh decades of life

| [http://www.disease-ontology.org/?id=DOID:0110420 DOID:0110420]

|

|

|

|-

| dopamine beta-hydroxylase deficiency

| class of disease

| autonomic nervous system disease
Congenital disorders of amino acid metabolism
inherited metabolic disorder
primary orthostatic hypotension
disorder of catecholamine synthesis
neurometabolic disease
ptosis
neurological disorder
genetic disease

| genetic metabolic disorder

| [http://www.disease-ontology.org/?id=DOID:0090145 DOID:0090145]

|

|

|

|-

| double pterygium

| class of disease

| pterygium

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10525 DOID:10525]

|

|

|

|-

| drug allergy

| class of disease

| allergy
drug intolerance

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060500 DOID:0060500]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.206 C20.543.206]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.100.468 C25.100.468]

|

|

|-

| drug psychosis

| class of disease

| drug-induced mental disorder
substance-induced psychosis
psychosis

| Psychotic organic mental disorders resulting from the toxic effect of drugs and chemicals or other harmful substance

| [http://www.disease-ontology.org/?id=DOID:1742 DOID:1742]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.723.809 C25.723.809]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.775.746 C25.775.746]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.700.675.600 F03.700.675.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.900.746 F03.900.746]

|

|

|-

| drug-induced hearing loss

| class of disease

| deafness

| nonsyndromic deafness that is characterized by cochlear or vestibular dysfunction resulting in loss of hearing caused by drug ototoxicity

| [http://www.disease-ontology.org/?id=DOID:0070310 DOID:0070310]

|

|

|

|-

| drug-induced hepatitis

| class of disease

| hepatitis
hepatotoxicity
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2044 DOID:2044]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.195.200 C06.552.195.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.100.562.200 C25.100.562.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.723.260.200 C25.723.260.200]

|

|

|-

| drug-induced lupus erythematosus

| class of disease
symptom or sign

| adverse drug reaction
lupus erythematosus
disease

| lupus erythematosus caused by chronic use of certain drugs

| [http://www.disease-ontology.org/?id=DOID:0040093 DOID:0040093]

|

|

| File:Procainamide.svg

|-

| drug-induced mental disorder

| class of disease

| substance-related disorder
adverse drug reaction
substance-induced psychosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1203 DOID:1203]

|

|

|

|-

| dry beriberi

| class of disease

| beriberi

| beriberi that is located in the nervous system and has symptom difficulty walking, numbness in extremities, tingling in extremities, paralysis of lower legs, difficulty speaking, confusion, and vomiting

| [http://www.disease-ontology.org/?id=DOID:0070318 DOID:0070318]

|

|

|

|-

| dry eye syndrome

| class of disease

| lacrimal apparatus disease

| corneal and conjunctival dryness due to deficient tear production

| [http://www.disease-ontology.org/?id=DOID:10140 DOID:10140]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.496.260 C11.496.260]

|

|

|-

| dumping syndrome

| class of disease

| postgastrectomy syndrome
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14495 DOID:14495]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.630.310 C06.405.748.630.310]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.767.812.500 C23.550.767.812.500]

|

|

|-

| duodenal atresia

| class of disease

| atresia
duodenal stenosis
atresia of small intestine
gastroduodenal malformation
intestinal atresia
disease

| congenital disorder of digestive system

| [http://www.disease-ontology.org/?id=DOID:0080216 DOID:0080216]

|

| Duodenal atresia

|

|-

| duodenal disease

| class of disease

| intestinal disease
small-intestine disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4072 DOID:4072]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.275 C06.405.469.275]

|

|

|-

| duodenal gastrinoma

| class of disease

| duodenum cancer
gastrinoma
duodenal neuroendocrine tumor, well differentiated, low or intermediate grade

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7959 DOID:7959]

|

|

|

|-

| duodenal neoplasm

| class of disease

| small intestine neoplasm
duodenal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1737 DOID:1737]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.476.411.445 C04.588.274.476.411.445]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.371.411.445 C06.301.371.411.445]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.249.411.445 C06.405.249.411.445]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.275.270 C06.405.469.275.270]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.491.445 C06.405.469.491.445]

| Duodenal neoplasms

|

|-

| duodenal obstruction

| class of disease

| duodenal disease
bowel obstruction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3558 DOID:3558]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.275.395 C06.405.469.275.395]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.531.311 C06.405.469.531.311]

|

|

|-

| duodenal somatostatinoma

| class of disease

| duodenum cancer
duodenal neuroendocrine tumor, well differentiated, low or intermediate grade

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7479 DOID:7479]

|

|

|

|-

| duodenal ulcer

| class of disease

| peptic ulcer disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1724 DOID:1724]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.275.800.348 C06.405.469.275.800.348]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.586.349 C06.405.748.586.349]

| Duodenal ulcers

|

|-

| duodenitis

| class of disease

| intestinal disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8643 DOID:8643]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.462.249 C06.405.205.462.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.275.600 C06.405.469.275.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.326.750 C06.405.469.326.750]

| Duodenitis

|

|-

| duodenum adenocarcinoma

| class of disease

| duodenum cancer
small intestine adenocarcinoma
adenocarcinoma

| duodenum cancer that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:10816 DOID:10816]

|

| Duodenal adenocarcinoma

|

|-

| duodenum adenoma

| class of disease

| duodenal neoplasm
adenoma of small intestine
duodenal disease
benign neoplasms by histologic type
adenoma

| duodenal benign neoplasm that has material basis in epithelial tissue with glandular origin

| [http://www.disease-ontology.org/?id=DOID:0050927 DOID:0050927]

|

|

|

|-

| duodenum cancer

| class of disease

| small intestine cancer
small intestine carcinoma
duodenal disease
duodenal neoplasm

| small intestine cancer that is located in the beginning section of the small intestine

| [http://www.disease-ontology.org/?id=DOID:10021 DOID:10021]

|

| Duodenal cancer

| File:Duodenal adenocarcinoma.png

|-

| dysembryoplastic neuroepithelial tumour

| class of disease

| neuronal and mixed glio-neuronal tumor
low grade glioma
central nervous system organ benign neoplasm
epilepsy

| type of brain tumour

| [http://www.disease-ontology.org/?id=DOID:2679 DOID:2679]

|

| Dysembryoplastic neuroepithelial tumour

| File:DNET HE.jpg

|-

| dysgammaglobulinemia

| class of disease

| selective immunoglobulin deficiency disease

| selective immunoglobulin deficiency disease that is caused by a reduction in some types of gamma globulins

| [http://www.disease-ontology.org/?id=DOID:11702 DOID:11702]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.147.333 C15.378.147.333]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.673.430 C20.673.430]

|

|

|-

| dysgerminoma

| class of disease

| germ cell cancer
ovarian cancer
disease

| germ cell cancer that derives from cells that give rise to egg cells

| [http://www.disease-ontology.org/?id=DOID:4441 DOID:4441]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.330.300 C04.557.465.330.300]

| Dysgerminoma

| File:Dysgerminoma, high mag.jpg

|-

| dysgerminoma of ovary

| class of disease

| dysgerminoma
ovarian primitive germ cell tumor

| dysgerminoma that is located in the ovary

| [http://www.disease-ontology.org/?id=DOID:5511 DOID:5511]

|

| Ovarian dysgerminoma

|

|-

| dysgraphia

| class of disease

| writing disorder
learning disability
disease

| developmental or acquired neurological condition

| [http://www.disease-ontology.org/?id=DOID:4540 DOID:4540]

|

| Dysgraphia

| File:Dysgraphia1.jpg

|-

| dyshormonogenic goiter

| class of disease

| goiter

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12175 DOID:12175]

|

|

|

|-

| dyskinesia of esophagus

| class of disease

| esophageal motility disorder
esophageal disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:9192 DOID:9192]

|

|

|

|-

| dyskinetic cerebral palsy

| class of disease

| cerebral palsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050672 DOID:0050672]

|

|

|

|-

| dysplastic nevus syndrome

| class of disease

| autosomal dominant disease
syndrome
disease

| Human skin disease

| [http://www.disease-ontology.org/?id=DOID:10041 DOID:10041]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.665.560.260 C04.557.665.560.260]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.700.305 C04.700.305]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.700.305 C16.320.700.305]

| Dysplastic nevus syndrome

|

|-

| dysthymic disorder

| class of disease

| mood disorder
disease

| psychological disorder

| [http://www.disease-ontology.org/?id=DOID:12139 DOID:12139]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.600.300.400 F03.600.300.400]

|

|

|-

| dystonia

| class of disease

| movement disorders
rare genetic dystonia
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:543 DOID:543]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.350.300 C10.597.350.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.350.300 C23.888.592.350.300]

| Dystonia

| File:Dystonia2010.JPG

|-

| dystonia 21

| class of disease

| dystonia
generalized isolated dystonia
genetic disease
autosomal dominant disease

| A dystonia characterized by autosomal dominant inheritance of late onset pure torsion dystonia that has material basis in variation in the chromosome region 2q14.3-q21.3.

| [http://www.disease-ontology.org/?id=DOID:0090046 DOID:0090046]

|

|

|

|-

| dystonia 5

| class of disease

| dystonia
genetic disease
autosomal dominant disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0090043 DOID:0090043]

|

|

|

|-

| dystransthyretinemic hyperthyroxinemia

| class of disease

| hyperthyroxinemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080219 DOID:0080219]

|

|

|

|-

| dystrophies primarily involving the retinal pigment epithelium

| class of disease

| fundus dystrophy
retinitis pigmentosa

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14252 DOID:14252]

|

|

|

|-

| ear disease

| class of disease

| sensory system disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:2742 DOID:2742]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.218 C09.218]

| Diseases and disorders of the ear and mastoid process

|

|-

| early congenital syphilis

| class of disease

| congenital syphilis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050488 DOID:0050488]

|

|

|

|-

| early infantile epileptic encephalopathy 1

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy characterized by X-linked recessive inheritance that has material basis in mutation in the ARX gene on chromosome Xp21

| [http://www.disease-ontology.org/?id=DOID:0080468 DOID:0080468]

|

|

|

|-

| early infantile epileptic encephalopathy 12

| class of disease

| Ohtahara syndrome

| An early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the PLCB1 gene on chromosome 20p12.3.

| [http://www.disease-ontology.org/?id=DOID:0080459 DOID:0080459]

|

|

|

|-

| early infantile epileptic encephalopathy 13

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the SCN8A gene on chromosome 12q13

| [http://www.disease-ontology.org/?id=DOID:0080445 DOID:0080445]

|

|

|

|-

| early infantile epileptic encephalopathy 14

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy characterized by refractory focal seizures developing by 6 months of age and arrest of psychomotor development that has material basis in heterozygous mutation in the KCNT1 gene on chromosome 9q34

| [http://www.disease-ontology.org/?id=DOID:0080439 DOID:0080439]

|

|

|

|-

| early infantile epileptic encephalopathy 16

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080449 DOID:0080449]

|

|

|

|-

| early infantile epileptic encephalopathy 19

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the GABRA1 gene on chromosome 5q34

| [http://www.disease-ontology.org/?id=DOID:0080431 DOID:0080431]

|

|

|

|-

| early infantile epileptic encephalopathy 2

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080467 DOID:0080467]

|

|

|

|-

| early infantile epileptic encephalopathy 21

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the NECAP1 gene on chromosome 12p13

| [http://www.disease-ontology.org/?id=DOID:0080443 DOID:0080443]

|

|

|

|-

| early infantile epileptic encephalopathy 23

| class of disease

| Ohtahara syndrome
autosomal recessive disease

| early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the DOCK7 gene on chromosome 1p31

| [http://www.disease-ontology.org/?id=DOID:0080415 DOID:0080415]

|

|

|

|-

| early infantile epileptic encephalopathy 24

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the HCN1 gene on chromosome 5p12

| [http://www.disease-ontology.org/?id=DOID:0080429 DOID:0080429]

|

|

|

|-

| early infantile epileptic encephalopathy 25

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the SLC13A5 gene on chromosome 17p13

| [http://www.disease-ontology.org/?id=DOID:0080453 DOID:0080453]

|

|

|

|-

| early infantile epileptic encephalopathy 26

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the KCNB1 gene on chromosome 20q13

| [http://www.disease-ontology.org/?id=DOID:0080461 DOID:0080461]

|

|

|

|-

| early infantile epileptic encephalopathy 27

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080444 DOID:0080444]

|

|

|

|-

| early infantile epileptic encephalopathy 29

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the AARS gene on chromosome 16q22

| [http://www.disease-ontology.org/?id=DOID:0080451 DOID:0080451]

|

|

|

|-

| early infantile epileptic encephalopathy 30

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the SIK1 gene on chromosome 21q22

| [http://www.disease-ontology.org/?id=DOID:0080465 DOID:0080465]

|

|

|

|-

| early infantile epileptic encephalopathy 31

| class of disease

| Ohtahara syndrome
developmental and epileptic encephalopathy

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the DNM1 gene on chromosome 9q34

| [http://www.disease-ontology.org/?id=DOID:0080437 DOID:0080437]

|

|

|

|-

| early infantile epileptic encephalopathy 32

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080416 DOID:0080416]

|

|

|

|-

| early infantile epileptic encephalopathy 33

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the EEF1A2 gene on chromosome 20q13

| [http://www.disease-ontology.org/?id=DOID:0080463 DOID:0080463]

|

|

|

|-

| early infantile epileptic encephalopathy 34

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080460 DOID:0080460]

|

|

|

|-

| early infantile epileptic encephalopathy 35

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080458 DOID:0080458]

|

|

|

|-

| early infantile epileptic encephalopathy 37

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080435 DOID:0080435]

|

|

|

|-

| early infantile epileptic encephalopathy 38

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in homozygous mutation in the ARV1 gene on chromosome 1q42

| [http://www.disease-ontology.org/?id=DOID:0080417 DOID:0080417]

|

|

|

|-

| early infantile epileptic encephalopathy 39

| class of disease

| Ohtahara syndrome

| infantile epileptic encephalopathy that has material basis in mutation in the SLC25A12 gene on chromosome 2q31

| [http://www.disease-ontology.org/?id=DOID:0080349 DOID:0080349]
[http://www.disease-ontology.org/?id=DOID:0080423 DOID:0080423]

|

|

|

|-

| early infantile epileptic encephalopathy 40

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the GUF1 gene on chromosome 4p12

| [http://www.disease-ontology.org/?id=DOID:0080427 DOID:0080427]

|

|

|

|-

| early infantile epileptic encephalopathy 41

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the SLC1A2 gene on chromosome 11p13

| [http://www.disease-ontology.org/?id=DOID:0080442 DOID:0080442]

|

|

|

|-

| early infantile epileptic encephalopathy 42

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the CACNA1A gene on chromosome 19p13

| [http://www.disease-ontology.org/?id=DOID:0080454 DOID:0080454]

|

|

|

|-

| early infantile epileptic encephalopathy 43

| class of disease

| Ohtahara syndrome
autosomal dominant disease

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the GABRB3 gene on chromosome 15q11

| [http://www.disease-ontology.org/?id=DOID:0080447 DOID:0080447]

|

|

|

|-

| early infantile epileptic encephalopathy 44

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the UBA5 gene on chromosome 3q22

| [http://www.disease-ontology.org/?id=DOID:0080424 DOID:0080424]

|

|

|

|-

| early infantile epileptic encephalopathy 45

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the GABRB1 gene on chromosome 4p13

| [http://www.disease-ontology.org/?id=DOID:0080428 DOID:0080428]

|

|

|

|-

| early infantile epileptic encephalopathy 46

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the GRIN2D gene on chromosome 19q13

| [http://www.disease-ontology.org/?id=DOID:0080456 DOID:0080456]

|

|

|

|-

| early infantile epileptic encephalopathy 47

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the FGF12 gene on chromosome 3q28

| [http://www.disease-ontology.org/?id=DOID:0080425 DOID:0080425]

|

|

|

|-

| early infantile epileptic encephalopathy 48

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080448 DOID:0080448]

|

|

|

|-

| early infantile epileptic encephalopathy 49

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080441 DOID:0080441]

|

|

|

|-

| early infantile epileptic encephalopathy 51

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy characterized by onset of intractable seizures and hypotonia in the first days or weeks of life that has material basis in homozygous or compound heterozygous mutation in the MDH2 gene on chromosome 7q11

| [http://www.disease-ontology.org/?id=DOID:0080433 DOID:0080433]

|

|

|

|-

| early infantile epileptic encephalopathy 52

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080455 DOID:0080455]

|

|

|

|-

| early infantile epileptic encephalopathy 53

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080464 DOID:0080464]

|

|

|

|-

| early infantile epileptic encephalopathy 54

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080418 DOID:0080418]

|

|

|

|-

| early infantile epileptic encephalopathy 55

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080283 DOID:0080283]

|

|

|

|-

| early infantile epileptic encephalopathy 56

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080282 DOID:0080282]

|

|

|

|-

| early infantile epileptic encephalopathy 57

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080284 DOID:0080284]

|

|

|

|-

| early infantile epileptic encephalopathy 58

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080285 DOID:0080285]

|

|

|

|-

| early infantile epileptic encephalopathy 59

| class of disease

| Ohtahara syndrome
infantile epileptic encephalopathy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080291 DOID:0080291]

|

|

|

|-

| early infantile epileptic encephalopathy 60

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the CNPY3 gene on chromosome 6p

| [http://www.disease-ontology.org/?id=DOID:0080432 DOID:0080432]

|

|

|

|-

| early infantile epileptic encephalopathy 61

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the ADAM22 gene on chromosome 7q21

| [http://www.disease-ontology.org/?id=DOID:0080434 DOID:0080434]

|

|

|

|-

| early infantile epileptic encephalopathy 62

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the SCN3A gene on chromosome 2q24

| [http://www.disease-ontology.org/?id=DOID:0080420 DOID:0080420]

|

|

|

|-

| early infantile epileptic encephalopathy 63

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in homozygous or compound heterozygous mutation in the CPLX1 gene on chromosome 4p16

| [http://www.disease-ontology.org/?id=DOID:0080426 DOID:0080426]

|

|

|

|-

| early infantile epileptic encephalopathy 65

| class of disease

| Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080430 DOID:0080430]

|

|

|

|-

| early infantile epileptic encephalopathy 66

| class of disease

| Ohtahara syndrome

| early infantile epileptic encephalopathy that has material basis in heterozygous mutation in the PACS2 gene on chromosome 14q32

| [http://www.disease-ontology.org/?id=DOID:0080446 DOID:0080446]

|

|

|

|-

| early infantile epileptic encephalopathy 8

| class of disease

| Ohtahara syndrome
hyperekplexia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080215 DOID:0080215]

|

|

|

|-

| early infantile epileptic encephalopathy 82

| class of disease

| autosomal recessive disease
Ohtahara syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080715 DOID:0080715]

|

|

|

|-

| early invasive cervical adenocarcinoma

| class of disease

| cervical adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8307 DOID:8307]

|

|

|

|-

| early onset absence epilepsy

| class of disease

| childhood electroclinical syndrome

| childhood electroclinical syndrome characterized by the occurrence of typical absence seizures starting between the age of four and ten years

| [http://www.disease-ontology.org/?id=DOID:0050708 DOID:0050708]

|

|

|

|-

| early yaws

| class of disease

| yaws

| A yaws that results in initial papule at the site of entry of bacteria. Without treatment, this is followed by disseminated skin lesions over the body. Bone pain and bone lesions may also occur.

| [http://www.disease-ontology.org/?id=DOID:10568 DOID:10568]

|

|

|

|-

| early-onset vitamin B6-dependent epilepsy

| class of disease

| autosomal recessive disease
epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080769 DOID:0080769]

|

|

|

|-

| eating disorder

| class of disease

| specific developmental disorder
nutrition disorder
disease

| habit of eating either insufficient or excessive food, to the detriment of health

| [http://www.disease-ontology.org/?id=DOID:8670 DOID:8670]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.400 F03.400]

| Eating disorder

|

|-

| eccrine acrospiroma

| class of disease

| eccrine sweat gland neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5442 DOID:5442]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.035.175.588 C04.557.470.035.175.588]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.550.175.588 C04.557.470.550.175.588]

|

|

|-

| eccrine adenocarcinoma

| class of disease

| eccrine sweat gland cancer
adenocarcinoma

| eccrine sweat gland cancer that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:4920 DOID:4920]

|

|

|

|-

| eccrine mixed tumor of skin

| class of disease

| eccrine sweat gland neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2079 DOID:2079]

|

| Chondroid syringoma

|

|-

| eccrine papillary adenocarcinoma

| class of disease

| eccrine adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5591 DOID:5591]

|

|

|

|-

| eccrine sweat gland cancer

| class of disease

| sweat gland cancer
eccrine sweat gland neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4921 DOID:4921]

|

|

|

|-

| eccrine sweat gland neoplasm

| class of disease

| sweat gland neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:173 DOID:173]

|

|

|

|-

| eclampsia

| class of disease

| pre-eclampsia
disease
life emergency

| pre-eclampsia characterized by the presence of seizures

| [http://www.disease-ontology.org/?id=DOID:13593 DOID:13593]
[http://www.disease-ontology.org/?id=DOID:12269 DOID:12269]
[http://www.disease-ontology.org/?id=DOID:12268 DOID:12268]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.395.124 C13.703.395.124]

| Eclampsia

| File:Dissection of uterus at term eclampsia.jpg

|-

| ecthyma

| class of disease

| impetigo

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11907 DOID:11907]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.410.890.168 C01.150.252.410.890.168]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.819.210 C01.150.252.819.210]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.800.720.210 C01.800.720.210]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.695.210 C17.800.695.210]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.838.765.210 C17.800.838.765.210]

| Ecthyma

|

|-

| ectodermal dysplasia 1

| class of disease

| hypohidrotic ectodermal dysplasia
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111664 DOID:0111664]

|

|

|

|-

| ectodermal dysplasia 10A

| class of disease

| hypohidrotic ectodermal dysplasia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111663 DOID:0111663]

|

|

|

|-

| ectodermal dysplasia 10B

| class of disease

| hypohidrotic ectodermal dysplasia
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111665 DOID:0111665]

|

|

|

|-

| ectodermal dysplasia 11B

| class of disease

| hypohidrotic ectodermal dysplasia
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111654 DOID:0111654]

|

|

|

|-

| ectodermal dysplasia 14

| class of disease

| autosomal recessive disease
ectodermal dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111662 DOID:0111662]

|

|

|

|-

| ectodermal dysplasia 15

| class of disease

| ectodermal dysplasia
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111651 DOID:0111651]

|

|

|

|-

| ectodermal dysplasia 4

| class of disease

| autosomal recessive disease
pure hair-nail type ectodermal dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111658 DOID:0111658]

|

|

|

|-

| ectodermal dysplasia 5

| class of disease

| pure hair-nail type ectodermal dysplasia
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111657 DOID:0111657]

|

|

|

|-

| ectodermal dysplasia 6

| class of disease

| autosomal recessive disease
pure hair-nail type ectodermal dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111659 DOID:0111659]

|

|

|

|-

| ectodermal dysplasia 7

| class of disease

| autosomal recessive disease
pure hair-nail type ectodermal dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111660 DOID:0111660]

|

|

|

|-

| ectodermal dysplasia 8

| class of disease

| autosomal recessive disease
ectodermal dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111661 DOID:0111661]

|

|

|

|-

| ectodermal dysplasia 9

| class of disease

| autosomal recessive disease
pure hair-nail type ectodermal dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111656 DOID:0111656]

|

|

|

|-

| ectomesenchymoma

| class of disease

| central nervous system mesenchymal non-meningothelial tumor
nervous system cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:4055 DOID:4055]

|

|

|

|-

| ectopic Cushing syndrome

| class of disease

| hyperaldosteronism
ACTH-dependent Cushing syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060890 DOID:0060890]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.730.713.317 C04.730.713.317]

|

|

|-

| ectopic pregnancy

| class of disease

| female reproductive system disease
human pregnancy
disease

| female reproductive system disease characterized by the implantation of the embryo outside the uterine cavity

| [http://www.disease-ontology.org/?id=DOID:0060329 DOID:0060329]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.733 C13.703.733]

| Ectopic pregnancy

| File:Tubal Pregnancy with embryo.jpg

|-

| ectopic thymus

| class of disease

| thymus gland disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6307 DOID:6307]

|

|

|

|-

| ectothrix infectious disease

| class of disease

| tinea capitis vale
hair diseases

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050097 DOID:0050097]

|

|

|

|-

| ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1

| class of disease

| ectrodactyly–ectodermal dysplasia–cleft syndrome

| An EEC syndrome characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 7q11.2-q21.3.

| [http://www.disease-ontology.org/?id=DOID:0060784 DOID:0060784]

|

|

|

|-

| ectrodactyly–ectodermal dysplasia–cleft syndrome

| class of disease

| autosomal dominant disease
ectodermal dysplasia
syndrome

| autosomal dominant disease characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefts (cleft lip-palate)

| [http://www.disease-ontology.org/?id=DOID:0060782 DOID:0060782]

|

|

|

|-

| ectropion

| class of disease

| eyelid disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1570 DOID:1570]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.338.362 C11.338.362]

| Ectropion

| File:Ectropion.JPG

|-

| eczematous dermatitis of eyelid

| class of disease

| noninfectious dermatoses of eyelid

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1893 DOID:1893]

|

|

|

|-

| egg allergy

| class of disease

| food allergy
health effects of eggs

| food allergy that is an allergy or hypersensitivity to dietary substances from the yolk or whites of eggs, causing an overreaction of the immune system which may lead to severe physical symptoms

| [http://www.disease-ontology.org/?id=DOID:4377 DOID:4377]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.370.150 C20.543.480.370.150]

|

| File:Fried egg, sunny side up.jpg

|-

| ego-dystonic sexual orientation

| class of disease

| gender dysphoria
disease

| psychiatric diagnosis

| [http://www.disease-ontology.org/?id=DOID:13352 DOID:13352]

|

|

|

|-

| electroclinical syndrome

| class of disease

| epilepsy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050701 DOID:0050701]

|

|

|

|-

| elephantiasis

| class of disease

| lymphedema

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4976 DOID:4976]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.496.320 C15.604.496.320]

| Elephantiasis

|

|-

| embryoma

| class of disease

| embryonal cancer

| carcinosarcoma and embryonal cancer that is located in embryonic tissue and results in a mass of rapidly growing cells

| [http://www.disease-ontology.org/?id=DOID:4766 DOID:4766]

|

| Embryonal tumors

|

|-

| embryonal cancer

| class of disease

| germ cell cancer

| germ cell cancer that is associated with an embryo

| [http://www.disease-ontology.org/?id=DOID:688 DOID:688]

|

|

|

|-

| embryonal carcinoma

| class of disease

| embryonal cancer
extragonadal germ cell cancer
extragonadal non-dysgerminomatous germ cell tumor
carcinoma
disease

| embryonal cancer that is a type of germ cell tumour, located in the ovaries or testes

| [http://www.disease-ontology.org/?id=DOID:3308 DOID:3308]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.200 C04.557.465.200]

| Embryonal carcinoma

|

|-

| embryonal extrahepatic bile duct rhabdomyosarcoma

| class of disease

| bile duct rhabdomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3253 DOID:3253]

|

|

|

|-

| embryonal rhabdomyosarcoma

| class of disease

| rhabdomyosarcoma
embryonal cancer

| rhabdomyosarcoma with mesenchymally-derived malignant cells resembling the developing skeletal muscle of the embryo

| [http://www.disease-ontology.org/?id=DOID:3246 DOID:3246]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.590.550.660.675 C04.557.450.590.550.660.675]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.550.660.675 C04.557.450.795.550.660.675]

|

|

|-

| embryonal testis carcinoma

| class of disease

| embryonal carcinoma
testicular cancer
testicular non-seminomatous germ cell cancer
testicular pure germ cell tumor

| embryonal carcinoma that is located in the testis

| [http://www.disease-ontology.org/?id=DOID:5680 DOID:5680]

|

|

|

|-

| emphysematous cholecystitis

| class of disease

| cystitis
cholecystitis

| bacterial infectious disease with inflammation of the gallbladder characterized by air-filled expansions in interstitial or subcutaneous tissues

| [http://www.disease-ontology.org/?id=DOID:9765 DOID:9765]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.564.263.500.500 C06.130.564.263.500.500]

|

|

|-

| enamel caries

| class of disease

| dental caries

| Human disease

| [http://www.disease-ontology.org/?id=DOID:217 DOID:217]

|

|

|

|-

| enamel erosion

| class of disease

| dental erosion

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2497 DOID:2497]

|

|

|

|-

| encapsulated thymoma

| class of disease

| thymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3278 DOID:3278]

|

|

| File:Encapsulated thymoma.jpg

|-

| encephalitis

| class of disease
symptom or sign

| brain inflammatory disease
encephalopathy
neurological symptom
disease

| acute inflammation of the brain with flu-like symptoms

| [http://www.disease-ontology.org/?id=DOID:9588 DOID:9588]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.430 C10.228.140.430]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.586.250 C10.586.250]

| Encephalitis

| File:Hsv encephalitis.jpg

|-

| encephalomalacia

| class of disease

| encephalopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2034 DOID:2034]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.461 C10.228.140.461]

|

|

|-

| encephalomyelitis

| class of disease

| central nervous system disease
inflammatory disease
disease

| inflammation of the brain and spinal cord

| [http://www.disease-ontology.org/?id=DOID:640 DOID:640]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.228.291 C10.228.228.291]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.440 C10.228.440]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.207.291 C01.207.291]

| Encephalomyelitis

|

|-

| encephalopathy

| class of disease

| central nervous system disease
disease

| central nervous system diseases located in the brain

| [http://www.disease-ontology.org/?id=DOID:936 DOID:936]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140 C10.228.140]

| Encephalopathy

|

|-

| encephalopathy due to defective mitochondrial and peroxisomal fission 1

| class of disease

| syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070347 DOID:0070347]

|

|

|

|-

| end stage renal failure

| class of disease

| chronic renal insufficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:783 DOID:783]

|

|

|

|-

| endemic goiter

| class of disease

| goiter
nutritional deficiency disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:13198 DOID:13198]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.874.283.300 C19.874.283.300]

|

|

|-

| endobronchial leiomyoma

| class of disease

| lung leiomyoma
bronchial neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6608 DOID:6608]

|

|

|

|-

| endobronchial lipoma

| class of disease

| bronchial neoplasm
respiratory system benign neoplasm
lipoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10183 DOID:10183]

|

|

|

|-

| endocardial fibroelastosis

| class of disease

| endocardium disease
familial restrictive cardiomyopathy
non-familial restrictive cardiomyopathy
non-familial dilated cardiomyopathy

| endocardium disease that is characterized by endocardium becoming massively fibrosed and thickened wih elastic tissue resulting in a restrictive cardiomyopathy.

| [http://www.disease-ontology.org/?id=DOID:12929 DOID:12929]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.238.281 C14.280.238.281]

|

|

|-

| endocarditis

| class of disease
symptom or sign

| endocardium disease
pancarditis
cardiovascular system symptom
disease

| endocardium disease characterized by inflammation of the endocardium of the heart chambers and valves

| [http://www.disease-ontology.org/?id=DOID:10314 DOID:10314]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.282 C14.280.282]

| Endocarditis

| File:Blood culture negative endocarditis.jpg

|-

| endocardium cancer

| class of disease

| heart cancer
neoplasm of endocardium
endocardium disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5877 DOID:5877]

|

|

|

|-

| endocervical adenocarcinoma

| class of disease

| endocervical carcinoma
adenocarcinoma

| endocervical carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:0050940 DOID:0050940]

|

| Endocervical adenocarcinoma

|

|-

| endocervical carcinoma

| class of disease

| cervix carcinoma
malignant neoplasm of endocervix

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7519 DOID:7519]

|

|

|

|-

| endocervical type cervical adenomyoma

| class of disease

| cervical adenomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8177 DOID:8177]

|

|

|

|-

| endocervical type cervical mucinous adenocarcinoma

| class of disease

| cervical mucinous adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8340 DOID:8340]

|

|

|

|-

| endocervicitis

| class of disease

| cervicitis
inflammatory disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5757 DOID:5757]

|

|

|

|-

| endocrine exophthalmos

| class of disease

| orbital disease
exophthalmos

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12359 DOID:12359]

|

|

|

|-

| endocrine gland cancer

| class of disease

| organ system cancer
endocrine gland neoplasm
endocrine system disease

| organ system cancer located in endocrine system that is characterized by uncontrolled cellular proliferation of the hormone producing glands of the endocrine system

| [http://www.disease-ontology.org/?id=DOID:170 DOID:170]

|

|

|

|-

| endocrine organ benign neoplasm

| class of disease

| organ system benign neoplasm
endocrine gland neoplasm
endocrine system disease

| organ system benign neoplasm that is located in endocrine glands which secretes a type of hormone directly into the bloodstream to regulate the body

| [http://www.disease-ontology.org/?id=DOID:0060089 DOID:0060089]

|

|

|

|-

| endocrine pancreas disease

| class of disease

| pancreas disease
endocrine system disease

| disease involving the endocrine pancreas

| [http://www.disease-ontology.org/?id=DOID:1428 DOID:1428]

|

|

|

|-

| endocrine system disease

| class of disease

| disease of anatomical entity
disease

| type of disease affecting the endocrine system

| [http://www.disease-ontology.org/?id=DOID:28 DOID:28]
[http://www.disease-ontology.org/?id=DOID:1922 DOID:1922]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19 C19]

| Endocrine diseases and disorders

| File:Illu endocrine system.png

|-

| endodermal sinus pattern testicular yolk sac tumor

| class of disease

| testicular yolk sac tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7302 DOID:7302]

|

|

|

|-

| endogenous depression

| class of disease

| major depressive disorder
endogenous mental disorder

| mental depression that is characterized by a dysregulation of the endogenous opioid system and not of the monaminergic system

| [http://www.disease-ontology.org/?id=DOID:1595 DOID:1595]

|

|

|

|-

| endometrial adenocarcinoma

| class of disease

| endometrial carcinoma
adenocarcinoma

| endometrial carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:2870 DOID:2870]

|

| Endometrial adenocarcinoma

|

|-

| endometrial adenosquamous carcinoma

| class of disease

| adenosquamous carcinoma
endometrial squamous cell carcinoma
squamous cell carcinoma
endometrial cancer

| endometrial carcinoma that derives from squamous cells and gland-like cells

| [http://www.disease-ontology.org/?id=DOID:5631 DOID:5631]

|

|

|

|-

| endometrial cancer

| class of disease

| uterine cancer
uterine corpus cancer
endometriosis
endometrial neoplasm
disease

| uterine cancer that is located in tissues lining the uterus

| [http://www.disease-ontology.org/?id=DOID:1380 DOID:1380]

|

| Endometrial cancer

| File:Endometrioid endometrial adenocarcinoma low mag.jpg

|-

| endometrial carcinoma

| class of disease

| endometrial cancer
carcinoma

| endometrial cancer that is located in the tissue lining the uterus

| [http://www.disease-ontology.org/?id=DOID:2871 DOID:2871]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.240 C04.557.470.200.025.240]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.945.418.948.585.124 C04.588.945.418.948.585.124]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.056.630.705.331 C13.351.500.056.630.705.331]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.937.418.685.331 C13.351.937.418.685.331]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.937.418.875.200.124 C13.351.937.418.875.200.124]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.630.705.331 C19.391.630.705.331]

|

|

|-

| endometrial clear cell adenocarcinoma

| class of disease

| endometrial adenocarcinoma
clear cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5299 DOID:5299]

|

|

|

|-

| endometrial disease

| class of disease

| uterine disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1005 DOID:1005]

|

| Diseases and disorders of endometrium

|

|-

| endometrial hyperplasia

| class of disease

| uterine benign neoplasm
endometrial disease
disease

| uterine benign neoplasm that is characterized by excessive proliferation of the cells of the endometrium

| [http://www.disease-ontology.org/?id=DOID:0080365 DOID:0080365]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.852.228 C13.351.500.852.228]

|

|

|-

| endometrial mixed adenocarcinoma

| class of disease

| endometrial adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7664 DOID:7664]

|

|

|

|-

| endometrial mucinous adenocarcinoma

| class of disease

| endometrial adenocarcinoma
mucinous adenocarcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:3707 DOID:3707]

|

|

|

|-

| endometrial small cell carcinoma

| class of disease

| uterine cancer
endometrial cancer
carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7139 DOID:7139]

|

|

|

|-

| endometrial squamous cell carcinoma

| class of disease

| endometrial carcinoma
squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5533 DOID:5533]

|

|

|

|-

| endometrial stromal nodule

| class of disease

| uterine benign neoplasm
endometrial stromal tumour

| human disease

| [http://www.disease-ontology.org/?id=DOID:1373 DOID:1373]

|

|

| File:EndometrialStromalNodule.JPG

|-

| endometrial stromal sarcoma

| class of disease

| endometrial stromal tumour

| human disease

| [http://www.disease-ontology.org/?id=DOID:4226 DOID:4226]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.435.775 C04.557.435.775]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.332.500 C04.557.450.795.332.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.852.762.200.500.500 C13.351.500.852.762.200.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.937.418.875.200.374.500 C13.351.937.418.875.200.374.500]

| Endometrial stromal sarcoma

|

|-

| endometrial stromal tumour

| class of disease

| endometrial cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:5166 DOID:5166]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.325 C04.557.450.565.325]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.332 C04.557.450.795.332]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.852.762.200.500 C13.351.500.852.762.200.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.937.418.875.200.374 C13.351.937.418.875.200.374]

|

|

|-

| endometrial transitional cell carcinoma

| class of disease

| endometrial carcinoma
transitional cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4005 DOID:4005]

|

|

|

|-

| endometrial type cervical adenomyoma

| class of disease

| cervical adenomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8178 DOID:8178]

|

|

|

|-

| endometrioid ovary carcinoma

| class of disease

| ovary adenocarcinoma
endometrial adenocarcinoma
uterine cancer
endometrial carcinoma
ovarian endometrial cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5828 DOID:5828]

|

|

|

|-

| endometriosis

| class of disease

| female reproductive system disease
endometrial disease
disease

| disease linked to the female reproductive system

| [http://www.disease-ontology.org/?id=DOID:289 DOID:289]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.500.163 C12.050.351.500.163]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.100.250.163 C12.100.250.163]

| Endometriosis

| File:Endometriosis.jpg

|-

| endometriosis of intestine

| class of disease

| endometriosis
intestinal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11428 DOID:11428]

|

| Endometriosis of intestine

|

|-

| endometriosis of ovary

| class of disease

| endometriosis
ovarian disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11432 DOID:11432]

|

|

|

|-

| endometriosis of pelvic peritoneum

| class of disease

| endometriosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11429 DOID:11429]

|

|

|

|-

| endometriosis of rectovaginal septum and vagina

| class of disease

| endometriosis
vaginal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11431 DOID:11431]

|

|

|

|-

| endometritis

| class of disease

| endometrial disease
disease

| inflammation of inner lining of uterus

| [http://www.disease-ontology.org/?id=DOID:1002 DOID:1002]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.056.750.249 C13.351.500.056.750.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.852.299 C13.351.500.852.299]

| Endometritis

| File:Endometritis - 2 - cropped - very high mag.jpg

|-

| endometrium carcinoma in situ

| class of disease

| in situ carcinoma
endometriosis
uterus carcinoma in situ

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5172 DOID:5172]

|

|

|

|-

| endomyocardial fibrosis

| class of disease

| restrictive cardiomyopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12932 DOID:12932]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.238.406 C14.280.238.406]

|

|

|-

| endophthalmitis

| class of disease

| globe disease
eye inflammation
disease

| globe disease that is characterized by inflammation of the inside of the eye

| [http://www.disease-ontology.org/?id=DOID:4692 DOID:4692]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.375.265 C01.375.265]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.294.265 C11.294.265]

|

|

|-

| endosalpingiosis

| class of disease

| endometriosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11427 DOID:11427]

|

| Endosalpingiosis

|

|-

| endothrix infectious disease

| class of disease

| tinea capitis vale
hair diseases

| tinea capitis that results in fungal infection located in hair, has material basis in Ascomycota fungi that belong to a group called dermatophytes, which produce arthroconidia within the hair shaft only

| [http://www.disease-ontology.org/?id=DOID:0050105 DOID:0050105]

|

|

|

|-

| enhanced S-cone syndrome

| class of disease

| retinal disease
vitreoretinal degeneration
unclassified primitive or secondary maculopathy
genetic disease
autosomal recessive disease

| Goldmann-Favre syndrome (GFS) is a vitreoretinal dystrophy characterized by early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular edema, retinoschisis)

| [http://www.disease-ontology.org/?id=DOID:0090059 DOID:0090059]

|

|

|

|-

| enophthalmos

| class of disease

| orbital disease
enophthalmia
disease

| posterior displacement of the eyeball within the orbit due to changes in the volume of the orbit (bone) relative to its contents

| [http://www.disease-ontology.org/?id=DOID:11175 DOID:11175]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.675.319 C11.675.319]

|

|

|-

| enteric pattern testicular yolk sac tumor

| class of disease

| testicular yolk sac tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8362 DOID:8362]

|

|

|

|-

| enterocele

| class of disease

| pelvic organ prolapse

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1283 DOID:1283]

|

| Enterocele

|

|-

| enthesopathy

| class of disease

| connective tissue disease
disease

| human disease: a disorder involving the attachment of a tendon or ligament to a bone

| [http://www.disease-ontology.org/?id=DOID:204 DOID:204]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.869.653 C05.651.869.653]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C26.874.800.750 C26.874.800.750]

| Enthesopathy

| File:EnthesopathyPelvisCT.png

|-

| entropion

| class of disease

| eyelid disease
disease

| medical condition in which the eyelid (usually the lower lid) folds inward

| [http://www.disease-ontology.org/?id=DOID:12397 DOID:12397]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.338.443 C11.338.443]

| Entropion

| File:Canine entropion.JPG

|-

| environmental induced asthma

| class of disease

| intrinsic asthma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080819 DOID:0080819]

|

|

|

|-

| eosinophilia-myalgia syndrome

| class of disease

| eosinophilia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:998 DOID:998]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.290 C05.651.290]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.491.387 C10.668.491.387]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.553.231.335 C15.378.553.231.335]

| Eosinophilia–myalgia syndrome

|

|-

| eosinophilic gastritis

| class of disease

| gastritis
chronic gastritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4030 DOID:4030]

|

|

|

|-

| eosinophilic meningitis

| class of disease

| chronic meningitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10361 DOID:10361]

|

|

|

|-

| eosinophilic pneumonia

| class of disease

| pneumonia
eosinophilia
disease

| disease in which an eosinophil, a type of white blood cell, accumulates in the lung

| [http://www.disease-ontology.org/?id=DOID:9498 DOID:9498]
[http://www.disease-ontology.org/?id=DOID:5870 DOID:5870]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.750 C08.381.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.553.231.549.750 C15.378.553.231.549.750]

|

|

|-

| eosinophilic variant of chromophobe renal cell carcinoma

| class of disease

| chromophobe renal cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6606 DOID:6606]

|

|

|

|-

| ependymal tumor

| class of disease

| ependymal tumor
cerebral ventricle cancer
carcinoma

| malignant glioma that is derived from ependymal cells, a type of glial cell, located in ventricle lining within the central part of the brain

| [http://www.disease-ontology.org/?id=DOID:5074 DOID:5074]

|

| Ependymal tumors

|

|-

| epicardium cancer

| class of disease

| pericardium cancer
neoplasm of epicardium

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4699 DOID:4699]

|

|

|

|-

| epicardium lipoma

| class of disease

| heart lipoma
lipoma
benign neoplasm of epicardium

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6284 DOID:6284]

|

|

|

|-

| epidermal appendage tumor

| class of disease

| skin benign neoplasm
Adnexal and skin appendage neoplasms
epidermal appendage disease

| neoplasms located in skin appendages

| [http://www.disease-ontology.org/?id=DOID:2433 DOID:2433]

|

|

|

|-

| epidermodysplasia verruciformis

| class of disease

| autosomal recessive disease
viral infectious disease
skin disease
immune deficiency with skin involvement
other immunodeficiency syndromes due to defects in innate immunity
primary immunodeficiency disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13777 DOID:13777]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.256.650.810.345 C01.925.256.650.810.345]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.825.810.260 C01.925.825.810.260]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.928.914.345 C01.925.928.914.345]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.838.790.810.260 C17.800.838.790.810.260]

| Epidermodysplasia verruciformis

| File:World's 4th a Tree Man.jpg

|-

| epidermolysis bullosa acquisita

| class of disease

| epidermolysis bullosa
pemphigoid
bullous skin disease
autoimmune skin disease

| chronic subepidermal blistering disease associated with autoimmunity to type VII collagen

| [http://www.disease-ontology.org/?id=DOID:4313 DOID:4313]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.831.493.080 C16.131.831.493.080]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.804.493.080 C17.800.804.493.080]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.827.275.080 C17.800.827.275.080]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.865.410.080 C17.800.865.410.080]

|

|

|-

| epidermolysis bullosa herpetiformis

| class of disease

| epidermolysis bullosa simplex
basal epidermolysis bullosa simplex
genetic disease
autosomal dominant disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060735 DOID:0060735]

|

|

|

|-

| epidermolysis bullosa with congenital localized absence of skin and deformity of nails

| class of disease

| dominant dystrophic epidermolysis bullosa
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111347 DOID:0111347]

|

|

|

|-

| epidermolytic acanthoma

| class of disease

| acanthoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4323 DOID:4323]

|

|

|

|-

| epidermolytic hyperkeratosis

| class of disease

| skin disease
congenital ichthyosiform erythroderma
keratinopathic ichthyosis

| rare and severe form of ichthyosis

| [http://www.disease-ontology.org/?id=DOID:4603 DOID:4603]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.831.512.400.375 C16.131.831.512.400.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.850.400.375 C16.320.850.400.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.614.492.400.375 C16.614.492.400.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.428.333.250.375 C17.800.428.333.250.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.804.512.400.375 C17.800.804.512.400.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.827.400.375 C17.800.827.400.375]

| Epidermolytic ichthyosis

| File:Epidermolytic hyperkeratosis new image.jpg

|-

| epididymal neoplasm

| class of disease

| male reproductive system neoplasm
epididymis disease
testicular cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:512 DOID:512]

|

|

|

|-

| epididymis adenocarcinoma

| class of disease

| epididymis cancer
adenocarcinoma

| epididymis cancer that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:10368 DOID:10368]

|

|

|

|-

| epididymis adenomatoid tumor

| class of disease

| male reproductive organ benign neoplasm
adenomatoid tumor
benign neoplasm of epididymis
adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:745 DOID:745]

|

|

|

|-

| epididymis cancer

| class of disease

| male reproductive organ cancer
epididymal neoplasm
epididymis disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10366 DOID:10366]

|

|

|

|-

| epididymis disease

| class of disease

| male reproductive system disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080373 DOID:0080373]

|

|

|

|-

| epidural abscess

| class of disease

| central nervous system disease
abscess
central nervous system cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:11387 DOID:11387]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.207.300 C01.207.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.228.300 C10.228.228.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.228.709.350 C10.228.228.709.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.854.303 C10.228.854.303]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.207.709.350 C01.207.709.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.830.025.325 C01.830.025.325]

|

|

|-

| epidural neoplasm

| class of disease

| Spinal cord cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3618 DOID:3618]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.614.250.803.342 C04.588.614.250.803.342]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.854.765.342 C10.228.854.765.342]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.551.240.750.200 C10.551.240.750.200]

|

|

|-

| epidural spinal canal angiolipoma

| class of disease

| angiolipoma
epidural neoplasm
cell type cancer
spinal cord disease
central nervous system organ benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3617 DOID:3617]

|

|

|

|-

| epidural spinal canal meningioma

| class of disease

| spinal canal and spinal cord meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3809 DOID:3809]

|

|

|

|-

| epiglottis neoplasm

| class of disease

| supraglottis neoplasm
neoplasm of hypopharynx

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7105 DOID:7105]

|

|

|

|-

| epilepsy

| class of disease
dictionary page in Wikipedia

| encephalopathy
disease

| human neurological disease causing seizures

| [http://www.disease-ontology.org/?id=DOID:1826 DOID:1826]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490 C10.228.140.490]

| Epilepsy

| File:Spike-waves.png

|-

| epilepsy, idiopathic generalized, susceptibility to, 8

| class of disease

| genetic disease
rare genetic epilepsy
generalized epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111322 DOID:0111322]

|

|

|

|-

| epiphora due to excess lacrimation

| class of disease

| excessive tearing

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14244 DOID:14244]

|

|

|

|-

| epiphora due to insufficient drainage

| class of disease

| excessive tearing

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13756 DOID:13756]

|

|

|

|-

| epiphyseal dysplasia, multiple, 6

| class of disease

| multiple epiphyseal dysplasia
genetic disease
multiple epiphyseal dysplasia due to collagen 9 anomaly
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070301 DOID:0070301]

|

|

|

|-

| epiretinal membrane

| class of disease

| retinal disease
degeneration of macula and posterior pole

| disease of the eye in response to changes in the vitreous humor or more rarely, diabetes

| [http://www.disease-ontology.org/?id=DOID:2006 DOID:2006]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.768.328 C11.768.328]

| Epiretinal membrane

|

|-

| episcleritis periodica fugax

| class of disease

| scleral disease
episcleritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12124 DOID:12124]

|

|

|

|-

| episodic kinesigenic dyskinesia 2

| class of disease

| dystonia
genetic disease
autosomal dominant disease

| A dystonia characterized by autosomal dominant inheritance of recurrent brief involuntary hyperkinesias triggered by sudden movements that has material basis in variation in the chromosome region 16q13-q22.1.

| [http://www.disease-ontology.org/?id=DOID:0090054 DOID:0090054]

|

|

|

|-

| epithelial and subepithelial dystrophy

| class of disease

| corneal dystrophy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060440 DOID:0060440]

|

|

|

|-

| epithelial malignant thymoma

| class of disease

| dendritic cell thymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7926 DOID:7926]

|

|

|

|-

| epithelial predominant Wilms' tumor

| class of disease

| nephroblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5189 DOID:5189]

|

|

|

|-

| epithelial predominant pulmonary blastoma

| class of disease

| pulmonary blastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4768 DOID:4768]

|

|

|

|-

| epithelial-myoepithelial carcinoma

| class of disease

| malignant epithelial tumor of salivary glands
salivary gland cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5309 DOID:5309]

|

| Epithelial-myoepithelial carcinoma

|

|-

| epithelial-stromal TGFBI dystrophy

| class of disease

| corneal dystrophy
stromal dystrophy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060441 DOID:0060441]

|

|

|

|-

| epithelioid cell melanoma

| class of disease

| melanoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4360 DOID:4360]

|

|

|

|-

| epithelioid cell synovial sarcoma

| class of disease

| synovial sarcoma
monophasic synovial sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5494 DOID:5494]

|

|

|

|-

| epithelioid inflammatory myofibroblastic sarcoma

| class of disease

| inflammatory myofibroblastic tumour

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080372 DOID:0080372]

|

|

|

|-

| epithelioid leiomyosarcoma

| class of disease

| leiomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5264 DOID:5264]

|

|

|

|-

| epithelioid malignant peripheral nerve sheath tumor

| class of disease

| malignant peripheral nerve sheath tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8353 DOID:8353]

|

|

|

|-

| epithelioid neurofibroma

| class of disease

| neurofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5149 DOID:5149]

|

|

|

|-

| epithelioid sarcoma

| class of disease

| soft-tissue sarcoma
connective tissue neoplasm
sarcoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:6193 DOID:6193]

|

| Epithelioid sarcoma

|

|-

| epithelioid trophoblastic tumor

| class of disease

| cervical uterine cancer
lung cancer
cell type cancer
gestational trophoblastic disease
trophoblastic neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3593 DOID:3593]

|

|

|

|-

| epithelioid type angiomyolipoma

| class of disease

| angiomyolipoma

| angiomyolipoma composed exclusively or predominantly by polygonal epithelioid cells with eosinophilic cytoplasm, often associated with cytologic atypia

| [http://www.disease-ontology.org/?id=DOID:3318 DOID:3318]

|

| Epithelioid angiomyolipoma

|

|-

| epithelioma cuniculatum

| class of disease

| verrucous carcinoma
Foot Dermatoses
cutaneous squamous-cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3751 DOID:3751]

|

|

|

|-

| epulis

| class of disease

| gingival overgrowth

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5337 DOID:5337]

|

| Epulis

|

|-

| equatorial staphyloma

| class of disease

| scleral staphyloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13788 DOID:13788]

|

|

|

|-

| erectile dysfunction

| class of disease
symptom or sign

| sexual dysfunction
reproductive system symptom
disease

| form of sexual dysfunction in males

| [http://www.disease-ontology.org/?id=DOID:1875 DOID:1875]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.100.500.214 C12.100.500.214]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.835.400 F03.835.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.100.875.486 C12.100.875.486]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.294.214 C12.200.294.214]

| Erectile dysfunction

| File:Erectile dysfunction.jpg

|-

| erythema elevatum diutinum

| class of disease

| vasculitis
reactive neutrophilic dermatose
immune complex mediated vasculitis

| vasculitis characterised by red, purple, brown or yellow papules (raised spot), plaques, or nodules, found on the backs of the hands, other extensor surfaces overlying joints, and on the buttocks

| [http://www.disease-ontology.org/?id=DOID:0060567 DOID:0060567]

|

| Erythema elevatum diutinum

|

|-

| erythema multiforme

| class of disease

| skin disease
erythema
allergy
disease

| skin disease that is a type of allergic reaction located in skin, which occurs in response to medications, infections, or illness

| [http://www.disease-ontology.org/?id=DOID:0050185 DOID:0050185]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.229.400 C17.800.229.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.865.475 C17.800.865.475]

| Erythema multiforme

|

|-

| erythema nodosum

| class of disease

| reactive neutrophilic dermatose
clinical sign
panniculitis
disease

| skin disease

| [http://www.disease-ontology.org/?id=DOID:0080750 DOID:0080750]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.174.600.375 C17.800.174.600.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.229.413 C17.800.229.413]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.206.380.375 C20.543.206.380.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.100.468.380.375 C25.100.468.380.375]

| Erythema nodosum

| File:An introduction to dermatology (1905) ERYTHEMA NODOSUM.jpg

|-

| erythematosquamous dermatosis

| class of disease

| skin disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9097 DOID:9097]

|

|

|

|-

| erythrasma

| class of disease

| pyoderma
Corynebacterium infection
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4131 DOID:4131]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.410.040.246.694 C01.150.252.410.040.246.694]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.819.320 C01.150.252.819.320]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.800.720.320 C01.800.720.320]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.838.765.320 C17.800.838.765.320]

| Erythrasma

| File:Erythrasma.jpg

|-

| erythrokeratodermia variabilis et progressiva 1

| class of disease

| autosomal dominant disease
autosomal recessive disease
erythrokeratodermia variabilis

| An erythrokeratodermia variabilis that has material basis in heterozygous, homozygous, or compound heterozygous mutation in GJB3 on 1p34.3.

| [http://www.disease-ontology.org/?id=DOID:0111195 DOID:0111195]

|

|

|

|-

| erythrokeratodermia variabilis et progressiva 2

| class of disease

| erythrokeratodermia variabilis
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080248 DOID:0080248]

|

|

|

|-

| erythrokeratodermia variabilis et progressiva 3

| class of disease

| erythrokeratodermia variabilis
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080249 DOID:0080249]

|

|

|

|-

| erythrokeratodermia variabilis et progressiva 4

| class of disease

| erythrokeratodermia variabilis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080250 DOID:0080250]

|

|

|

|-

| erythrokeratodermia variabilis et progressiva 5

| class of disease

| erythrokeratodermia variabilis
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080251 DOID:0080251]

|

|

|

|-

| erythrokeratodermia variabilis et progressiva 6

| class of disease

| erythrokeratodermia variabilis
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080766 DOID:0080766]

|

|

|

|-

| erythropoietin polycythemia

| class of disease

| acquired polycythemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2839 DOID:2839]

|

|

|

|-

| esophageal adenoid cystic carcinoma

| class of disease

| esophageal carcinoma

| esophageal carcinoma that derives from epithelial cells of the salivary gland

| [http://www.disease-ontology.org/?id=DOID:4878 DOID:4878]

|

|

|

|-

| esophageal adenosquamous carcinoma

| class of disease

| adenosquamous carcinoma
squamous cell carcinoma
esophageal cancer

| esophageal carcinoma that derives from squamous cells and gland-like cells

| [http://www.disease-ontology.org/?id=DOID:5625 DOID:5625]

|

|

|

|-

| esophageal basaloid squamous cell carcinoma

| class of disease

| basaloid squamous cell carcinoma
esophageal cancer
squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7051 DOID:7051]

|

|

|

|-

| esophageal cancer

| class of disease

| esophageal neoplasm
esophageal disease
gastrointestinal system cancer
disease

| gastrointestinal system cancer that is located in the esophagus

| [http://www.disease-ontology.org/?id=DOID:5041 DOID:5041]

|

| Esophageal cancer

| File:Esophageal adenoca.jpg

|-

| esophageal candidiasis

| class of disease

| candidiasis
fungal esophagitis
esophageal disease

| candidiasis that involves fungal infection of the esophagus by Candida albicans in immunocompromised people, resulting in lesions, bleeding, painful swallowing and substernal pain

| [http://www.disease-ontology.org/?id=DOID:13146 DOID:13146]

|

| Esophageal candidiasis

|

|-

| esophageal carcinoma

| class of disease

| esophageal cancer
carcinoma

| esophageal cancer that has material basis in abnormally proliferating cells derives from epithelial cells

| [http://www.disease-ontology.org/?id=DOID:1107 DOID:1107]

|

|

|

|-

| esophageal disease

| class of disease

| gastrointestinal system disease

| gastrointestinal system disease that is located in the esophagus

| [http://www.disease-ontology.org/?id=DOID:6050 DOID:6050]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.117 C06.405.117]

| Diseases and disorders of the esophagus

|

|-

| esophageal diverticulosis

| class of disease

| esophageal disease
esophageal diverticulum

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13185 DOID:13185]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.117.136 C06.405.117.136]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.282.500.438 C06.405.205.282.500.438]

|

|

|-

| esophageal leukoplakia

| class of disease

| esophageal disease
leukoplakia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9021 DOID:9021]

|

|

|

|-

| esophageal neuroendocrine tumor

| class of disease

| esophageal cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5784 DOID:5784]

|

|

|

|-

| esophageal varix

| class of disease

| vein disorder
esophageal disease
esophageal and gastric varices
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:112 DOID:112]

|

| Esophageal varices

| File:Esophageal varices - wale.jpg

|-

| esophagus adenocarcinoma

| class of disease

| esophageal carcinoma
adenocarcinoma

| esophageal carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:4914 DOID:4914]

|

| Adenocarcinomas of esophagus

|

|-

| esophagus carcinoma in situ

| class of disease

| in situ carcinoma
esophageal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9095 DOID:9095]

|

|

|

|-

| esophagus leiomyoma

| class of disease

| benign neoplasm of esophagus
esophageal disease
gastrointestinal system benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:960 DOID:960]

|

|

|

|-

| esophagus leiomyosarcoma

| class of disease

| esophagus sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5276 DOID:5276]

|

|

|

|-

| esophagus liposarcoma

| class of disease

| esophagus sarcoma
liposarcoma
esophageal cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5694 DOID:5694]

|

|

|

|-

| esophagus small cell carcinoma

| class of disease

| esophageal carcinoma
esophageal neuroendocrine tumor
inherited neuroendocrine tumor
small cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7134 DOID:7134]

|

|

|

|-

| esophagus squamous cell carcinoma

| class of disease

| esophageal carcinoma
squamous cell carcinoma

| esophageal carcinoma that derives from epithelial squamous cells located in the esophagus

| [http://www.disease-ontology.org/?id=DOID:3748 DOID:3748]

|

| Squamous-cell carcinoma of esophagus

|

|-

| esophagus squamous cell papilloma

| class of disease

| benign neoplasm of esophagus
esophageal disease
gastrointestinal system benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:959 DOID:959]

|

| Esophageal squamous papilloma

|

|-

| esophagus verrucous carcinoma

| class of disease

| esophagus squamous cell carcinoma
verrucous carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3747 DOID:3747]

|

|

|

|-

| esotropia

| class of disease

| strabismus

| Esotropia is a strabismus in which the eye turns inward toward the nose

| [http://www.disease-ontology.org/?id=DOID:9840 DOID:9840]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.562.887.300 C10.292.562.887.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.590.810.400 C11.590.810.400]

| Esotropia

| File:Andre Filipe Teixeira Marques Esotropia.jpg

|-

| essential hypertension

| class of disease

| arterial hypertension
disease

| hypertension with no known cause, the most common type of hypertension

| [http://www.disease-ontology.org/?id=DOID:10825 DOID:10825]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.489.165 C14.907.489.165]

|

|

|-

| essential tremor 1

| class of disease

| autosomal dominant disease
essential tremor

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111428 DOID:0111428]

|

|

|

|-

| essential tremor 2

| class of disease

| autosomal dominant disease
essential tremor

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111429 DOID:0111429]

|

|

|

|-

| essential tremor 3

| class of disease

| essential tremor

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111430 DOID:0111430]

|

|

|

|-

| essential tremor 4

| class of disease

| essential tremor
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111431 DOID:0111431]

|

|

|

|-

| essential tremor 5

| class of disease

| essential tremor
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111432 DOID:0111432]

|

|

|

|-

| esthesioneuroblastoma

| class of disease

| blastoma
head and neck cancer
olfactory nerve neoplasm
disease

| rare cancer of the nasal cavity

| [http://www.disease-ontology.org/?id=DOID:369 DOID:369]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.600.590.650.550.150 C04.557.465.625.600.590.650.550.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.670.590.650.550.150 C04.557.470.670.590.650.550.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.600.590.650.550.150 C04.557.580.625.600.590.650.550.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.650.200 C10.292.650.200]

|

|

|-

| estrogen excess

| class of disease

| ovarian dysfunction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14336 DOID:14336]

|

|

|

|-

| estrogen-receptor negative breast cancer

| class of disease

| breast cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060076 DOID:0060076]

|

|

|

|-

| estrogen-receptor positive breast cancer

| class of disease

| breast cancer
Hormone receptor positive breast tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060075 DOID:0060075]

|

|

|

|-

| ethmoid sinus adenocarcinoma

| class of disease

| ethmoid sinus cancer
adenocarcinoma

| ethmoid sinus cancer that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:2766 DOID:2766]

|

|

|

|-

| ethmoid sinus cancer

| class of disease

| paranasal sinus cancer
ethmoidal sinus neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1363 DOID:1363]

|

|

|

|-

| ethmoid sinus squamous cell carcinoma

| class of disease

| ethmoid sinus cancer
squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2763 DOID:2763]

|

|

|

|-

| ethmoid sinusitis

| class of disease

| sinusitis

| sinusitis which involves infection of ethmoid sinuses that causes pain or pressure behind and between the eyes, tearing, and headache over the forehead

| [http://www.disease-ontology.org/?id=DOID:9507 DOID:9507]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.460.692.752.267 C08.460.692.752.267]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.730.749.267 C08.730.749.267]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.603.692.752.267 C09.603.692.752.267]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.748.749.267 C01.748.749.267]

|

|

|-

| ethmoidal sinus neoplasm

| class of disease

| paranasal sinus neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1364 DOID:1364]

|

|

|

|-

| eumycotic mycetoma

| class of disease

| dermatomycosis
mycetoma
disease

| chronic granulomatous fungal disease of humans

| [http://www.disease-ontology.org/?id=DOID:13078 DOID:13078]

|

| Madura foot

| File:Madura foot..JPG

|-

| eunuchism

| class of disease

| hypogonadism, male
hypogonadism
disease

| hypogonadism that is characterized by the lack of mature male germ cells and testicular hormones

| [http://www.disease-ontology.org/?id=DOID:5003 DOID:5003]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.482.293 C19.391.482.293]

| Eunuchoidism

|

|-

| euthyroid sick syndrome

| class of disease

| thyroid gland disease

| Secondary allostasis of thyroid function in fetal life, starving and in critical illness

| [http://www.disease-ontology.org/?id=DOID:2856 DOID:2856]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.874.255 C19.874.255]

|

|

|-

| eversion of lacrimal punctum

| class of disease

| lacrimal apparatus disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13651 DOID:13651]

|

|

|

|-

| exanthem

| class of disease
symptom or sign

| skin disease
rash
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050486 DOID:0050486]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.257 C17.800.257]

| Exanthem

| File:Severerash.jpg

|-

| exanthema subitum

| class of disease

| viral infectious disease
Roseolovirus infectious disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050495 DOID:0050495]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.256.466.850.290 C01.925.256.466.850.290]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.825.290 C01.925.825.290]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.257.335 C17.800.257.335]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.838.790.290 C17.800.838.790.290]

| Roseola

| File:Hhv-6 (1).jpg

|-

| excessive tearing

| class of disease
symptom or sign

| lacrimal apparatus disease
tear secretion
eye symptom
disease

| overflow of tears onto the face

| [http://www.disease-ontology.org/?id=DOID:13757 DOID:13757]

|

| Epiphora (medicine)

|

|-

| excoriation

| class of disease
symptom or sign

| dermatitis
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:9165 DOID:9165]

|

|

|

|-

| exercise-induced bronchoconstriction

| class of disease

| asthma
dyspnea on effort
intrinsic asthma

| medical condition

| [http://www.disease-ontology.org/?id=DOID:0080821 DOID:0080821]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.127.108.110 C08.127.108.110]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.674.095.110 C08.674.095.110]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.680.095.110 C20.543.480.680.095.110]

|

|

|-

| exfoliation syndrome

| class of disease

| iris disease
hereditary glaucoma
phacogenic glaucoma

| syndrome that occurs when tiny flakes of dandruff-like material build up in the body and are found in the heart, kidneys, liver, lungs, and eye

| [http://www.disease-ontology.org/?id=DOID:13641 DOID:13641]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.375.285 C11.941.375.285]

|

|

|-

| exocervical carcinoma

| class of disease

| cervix carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2892 DOID:2892]

|

|

|

|-

| exocrine pancreatic insufficiency

| class of disease

| pancreas disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13316 DOID:13316]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.689.276 C06.689.276]

|

|

|-

| exophthalmic ophthalmoplegia

| class of disease

| ophthalmoplegia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13135 DOID:13135]

|

|

|

|-

| exostosis

| class of disease

| hyperostosis

| hyperostosis that involves formation of new bone on the surface of preexisting bone

| [http://www.disease-ontology.org/?id=DOID:203 DOID:203]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.540.310 C05.116.540.310]

| Exostoses

| File:Exostose Femur 54jm- CT cor und VR - 001.svg

|-

| exotropia

| class of disease

| strabismus

| form of strabismus where the eyes are deviated outward

| [http://www.disease-ontology.org/?id=DOID:1143 DOID:1143]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.562.887.650 C10.292.562.887.650]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.590.810.440 C11.590.810.440]

| Exotropia

|

|-

| exposure keratitis

| class of disease

| keratoconjunctivitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9461 DOID:9461]

|

|

|

|-

| expressive language disorder

| class of disease

| language disorder
specific language impairment-5

| neurodevelopmental condition

| [http://www.disease-ontology.org/?id=DOID:11385 DOID:11385]

|

|

|

|-

| external auditory meatus lipoma

| class of disease

| sensory organ benign neoplasm
lipoma
external ear neoplasm
benign neoplasm of ear

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10203 DOID:10203]

|

|

|

|-

| external resorption

| class of disease

| tooth resorption

| human disease

| [http://www.disease-ontology.org/?id=DOID:14529 DOID:14529]

|

|

|

|-

| extra-adrenal pheochromocytoma

| class of disease

| malignant pheochromocytoma

| adrenal medulla cancer that originate in the ganglia of the sympathetic nervous system and are named based upon the primary anatomical site of origin

| [http://www.disease-ontology.org/?id=DOID:0050936 DOID:0050936]

|

|

|

|-

| extracranial neuroblastoma

| class of disease

| neuroblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:371 DOID:371]

|

|

|

|-

| extracutaneous mastocytoma

| class of disease

| systemic mastocytosis
mastocytoma
connective tissue neoplasm
benign mastocytoma
genetic hematologic disease
rare genetic immune disease
inherited tumor
rare genetic bone disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4659 DOID:4659]

|

|

|

|-

| extragonadal germ cell cancer

| class of disease

| germ cell cancer
extragonadal germ cell tumor

| A germ cell cancer that derives from germ cells that are found in areas of the body other than the ovary or testicle. The tumors originate in the sperm forming cells in the testicles or egg producing cells in the ovary.

| [http://www.disease-ontology.org/?id=DOID:4717 DOID:4717]

|

|

|

|-

| extragonadal nonseminomatous germ cell tumor

| class of disease

| extragonadal germ cell cancer
brain cancer
mediastinal cancer
extragonadal non-dysgerminomatous germ cell tumor
germ cell cancer
nongerminomatous germ cell tumor

| extragonadal germ cell cancer that are located in the pineal gland in the brain, located in the mediastinum or located in the abdomen

| [http://www.disease-ontology.org/?id=DOID:5677 DOID:5677]

|

|

|

|-

| extragonadal seminoma

| class of disease

| seminoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5838 DOID:5838]

|

|

|

|-

| extrahepatic bile duct adenocarcinoma

| class of disease

| extrahepatic bile duct carcinoma
adenocarcinoma
bile duct adenocarcinoma

| extrahepatic bile duct carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:3495 DOID:3495]

|

|

|

|-

| extrahepatic bile duct adenoma

| class of disease

| bile duct adenoma
biliary tract neoplasm

| bile duct ademona and neoplasm of extrahepatic bile duct that are composed of papillary, tubular, or combined tubulopapillary structures lined by dysplastic epithelium

| [http://www.disease-ontology.org/?id=DOID:5438 DOID:5438]

|

|

|

|-

| extrahepatic bile duct carcinoma

| class of disease

| bile duct carcinoma
bile duct cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4682 DOID:4682]

|

|

|

|-

| extrahepatic bile duct cystadenoma

| class of disease

| bile duct cystadenoma
extrahepatic bile duct adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8105 DOID:8105]

|

|

|

|-

| extrahepatic bile duct leiomyoma

| class of disease

| leiomyoma
bile duct disease
biliary tract neoplasm
liver leiomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5125 DOID:5125]

|

|

|

|-

| extrahepatic bile duct leiomyosarcoma

| class of disease

| bile duct sarcoma
leiomyosarcoma
extrahepatic bile duct carcinoma
liver leiomyosarcoma

| leiomyosarcoma and sarcoma of bile duct that is located in the bile duct or located in the outside of the liver

| [http://www.disease-ontology.org/?id=DOID:5293 DOID:5293]

|

|

|

|-

| extrahepatic bile duct lipoma

| class of disease

| biliary tract neoplasm
lipoma
bile duct disease
liver lipoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:10209 DOID:10209]

|

|

|

|-

| extrahepatic bile duct papillary adenoma

| class of disease

| extrahepatic bile duct adenoma
biliary papillomatosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7503 DOID:7503]

|

|

|

|-

| extrahepatic bile duct small cell adenocarcinoma

| class of disease

| extrahepatic bile duct adenocarcinoma
liver neuroendocrine carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5926 DOID:5926]

|

|

|

|-

| extrahepatic biliary papillomatosis

| class of disease

| biliary papillomatosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7752 DOID:7752]

|

|

|

|-

| extrahepatic cholestasis

| class of disease

| cholestasis
non-neoplastic bile duct disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13619 DOID:13619]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.120.135.150 C06.130.120.135.150]

|

|

|-

| extramedullary plasmacytoma

| class of disease

| plasmacytoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3720 DOID:3720]

|

|

|

|-

| extranodal NK/T-cell lymphoma, nasal type

| class of disease

| T-cell lymphoma
mature T-cell and NK-cell lymphoma
nasal cavity cancer

| medical condition

| [http://www.disease-ontology.org/?id=DOID:0080797 DOID:0080797]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386.480.750.199 C04.557.386.480.750.199]

|

|

|-

| extraosseous Ewing's sarcoma

| class of disease

| Ewing sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4232 DOID:4232]

|

|

|

|-

| extraosseous Ewings sarcoma-primitive neuroepithelial tumor

| class of disease

| extraosseous Ewing's sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4985 DOID:4985]

|

|

|

|-

| extraosseous chondrosarcoma

| class of disease

| chondrosarcoma

| chondrosarcoma that is located in exclusively soft tissue

| [http://www.disease-ontology.org/?id=DOID:4549 DOID:4549]

|

|

|

|-

| extraosseous osteosarcoma

| class of disease

| osteosarcoma
connective tissue neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3357 DOID:3357]

|

|

|

|-

| extrapulmonary tuberculosis

| class of disease

| tuberculosis

| respiratory disease

| [http://www.disease-ontology.org/?id=DOID:0050598 DOID:0050598]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.410.040.552.846.617 C01.150.252.410.040.552.846.617]

| Extrapulmonary tuberculosis

| File:Mal de POTT esp.jpg

|-

| extrapyramidal and movement disorder

| class of disease

| movement disorders
neurological disorder

| disease of the nervous system

| [http://www.disease-ontology.org/?id=DOID:13839 DOID:13839]

|

|

|

|-

| extraskeletal chondroma

| class of disease

| connective tissue benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3814 DOID:3814]

|

|

|

|-

| extraskeletal mesenchymal chondrosarcoma

| class of disease

| extraosseous chondrosarcoma
mesenchymal chondrosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4548 DOID:4548]

|

|

|

|-

| extraskeletal myxoid chondrosarcoma

| class of disease

| extraosseous chondrosarcoma
myxoid chondrosarcoma

| extraosseous chondrosarcoma that has material basis in cells derived from transformed cells that produce cartilage and is characterized by a marked abundance of extracellular mucoid (myxoid) matrix

| [http://www.disease-ontology.org/?id=DOID:6496 DOID:6496]

|

|

|

|-

| extratemporal epilepsy

| class of disease

| epilepsy
focal epilepsy

| epilepsy syndrome that is located in an area of the brain other than the temporal lobe

| [http://www.disease-ontology.org/?id=DOID:2544 DOID:2544]

|

|

|

|-

| extrinsic allergic alveolitis

| class of disease
symptom or sign

| occupational disease
interstitial lung disease
allergy
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:841 DOID:841]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.483.125 C08.381.483.125]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.674.055 C08.674.055]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.680.075 C20.543.480.680.075]

| Hypersensitivity pneumonitis

| File:Chronic hypersensitivity pneumonitis - histology.jpg

|-

| extrinsic asthma

| class of disease

| chronic asthma
allergy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080811 DOID:0080811]

|

|

|

|-

| exudative glomerulonephritis

| class of disease

| glomerulonephritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4777 DOID:4777]

|

|

|

|-

| exudative vitreoretinopathy 1

| class of disease

| exudative vitreoretinopathy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111412 DOID:0111412]

|

|

|

|-

| exudative vitreoretinopathy 3

| class of disease

| exudative vitreoretinopathy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111409 DOID:0111409]

|

|

|

|-

| exudative vitreoretinopathy 4

| class of disease

| exudative vitreoretinopathy
autosomal genetic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111411 DOID:0111411]

|

|

|

|-

| exudative vitreoretinopathy 5

| class of disease

| exudative vitreoretinopathy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111408 DOID:0111408]

|

|

|

|-

| exudative vitreoretinopathy 6

| class of disease

| exudative vitreoretinopathy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111410 DOID:0111410]

|

|

|

|-

| exudative vitreoretinopathy 7

| class of disease

| exudative vitreoretinopathy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080264 DOID:0080264]

|

|

|

|-

| eye accommodation disease

| class of disease

| eye disease
refraction or accommodation disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10034 DOID:10034]

|

|

|

|-

| eye carcinoma

| class of disease

| ocular cancer
carcinoma

| ocular cancer that has material basis in abnormally proliferating cells, derives from epithelial cells and arises from the tissues that cover structures located in the eye

| [http://www.disease-ontology.org/?id=DOID:295 DOID:295]

|

|

|

|-

| eye degenerative disease

| class of disease

| eye disease
degenerative disease

| neurodegenerative disease that involves the eye

| [http://www.disease-ontology.org/?id=DOID:9799 DOID:9799]

|

|

|

|-

| eye disease

| class of disease

| eye and adnexa disease
sensory system disease
organ-specific disease

| health condition negatively affecting the eye

| [http://www.disease-ontology.org/?id=DOID:5614 DOID:5614]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11 C11]

| Diseases and disorders of the eye and adnexa

|

|-

| eyelid disease

| class of disease

| eye adnexa disease
skin disease

| adnexa disease that is located in the eyelid

| [http://www.disease-ontology.org/?id=DOID:530 DOID:530]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.338 C11.338]

|

|

|-

| eyelid neoplasm

| class of disease

| skin neoplasm
eyelid disease
facial neoplasm
skin benign neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:2173 DOID:2173]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.443.392.500 C04.588.443.392.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.319.421 C11.319.421]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.338.526 C11.338.526]

|

|

|-

| facial dermatosis

| class of disease

| skin disease
head and neck disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3134 DOID:3134]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.271 C17.800.271]

|

|

|-

| facial nerve disease

| class of disease

| cranial nerve disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1756 DOID:1756]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.299 C07.465.299]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.319 C10.292.319]

|

|

|-

| facial nerve neoplasm

| class of disease

| cranial nerve neoplasm
facial nerve disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1760 DOID:1760]

|

| Facial nerve neoplasms

|

|-

| facial neuralgia

| class of disease

| neuralgia
facial nerve disease
orofacial pain
cranial neuralgia

| human disease

| [http://www.disease-ontology.org/?id=DOID:13865 DOID:13865]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.299.625 C07.465.299.625]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.319.625 C10.292.319.625]

|

|

|-

| facioscapulohumeral muscular dystrophy

| class of disease

| muscular dystrophy
disease

| Muscular dystrophy that classically weakens the muscles of the face (facio), shoulder girdle (scapulo) and upper arm (humerus). Weakness usually is asymmetrical and develops in other areas of the body as well, such as the abdomen and shin.

| [http://www.disease-ontology.org/?id=DOID:11727 DOID:11727]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.534.500.400 C05.651.534.500.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.491.175.500.400 C10.668.491.175.500.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.577.400 C16.320.577.400]

| Facioscapulohumeral muscular dystrophy

|

|-

| facioscapulohumeral muscular dystrophy 1

| class of disease

| facioscapulohumeral muscular dystrophy

| facioscapulohumeral muscular dystrophy that has material basis in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35

| [http://www.disease-ontology.org/?id=DOID:0111192 DOID:0111192]

|

|

|

|-

| facioscapulohumeral muscular dystrophy 2

| class of disease

| digenic disease
facioscapulohumeral muscular dystrophy

| A facioscapulohumeral muscular dystrophy that has material basis in digenic inheritance of a heterozygous mutation in SMCHDI on 18p11.32 and a haplotype on chromosome 4 that is permissive for DUX4 expression.

| [http://www.disease-ontology.org/?id=DOID:0111193 DOID:0111193]

|

|

|

|-

| factitious disorder

| class of disease

| mental disorder

| disease of mental health where symptoms are deliberately produced, feigned or exaggerated in order to falsely demonstrate the presence of an illness

| [http://www.disease-ontology.org/?id=DOID:1766 DOID:1766]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.875.375 F03.875.375]

| Factitious disorders

|

|-

| factor VII deficiency

| class of disease

| inherited blood coagulation disease
blood coagulation disease
autosomal recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2215 DOID:2215]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100.100.310 C15.378.100.100.310]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100.141.310 C15.378.100.141.310]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463.310 C15.378.463.310]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.099.310 C16.320.099.310]

|

|

|-

| factor X deficiency

| class of disease

| inherited blood coagulation disease
blood coagulation disease
autosomal recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2222 DOID:2222]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100.100.320 C15.378.100.100.320]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100.141.320 C15.378.100.141.320]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463.320 C15.378.463.320]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.099.320 C16.320.099.320]

|

|

|-

| fallopian tube adenocarcinoma

| class of disease

| fallopian tube carcinoma
adenocarcinoma

| fallopian tube carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:3706 DOID:3706]

|

|

|

|-

| fallopian tube adenofibroma

| class of disease

| fallopian tube benign neoplasm
adenofibroma
serous adenofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5478 DOID:5478]

|

|

|

|-

| fallopian tube adenomatoid tumor

| class of disease

| fallopian tube benign neoplasm
adenomatoid tumor
adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5196 DOID:5196]

|

| Adenomatoid tumor of fallopian tube

|

|-

| fallopian tube adenosarcoma

| class of disease

| fallopian tube carcinosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1973 DOID:1973]

|

|

|

|-

| fallopian tube benign neoplasm

| class of disease

| female reproductive organ benign neoplasm
fallopian tube neoplasm
fallopian tube disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060111 DOID:0060111]

|

|

|

|-

| fallopian tube cancer

| class of disease

| female reproductive organ cancer
fallopian tube neoplasm
fallopian tube disease

| female reproductive organ cancer that is located in fallopian tube

| [http://www.disease-ontology.org/?id=DOID:1964 DOID:1964]

|

| Fallopian tube cancer

|

|-

| fallopian tube carcinoma

| class of disease

| fallopian tube cancer
carcinoma

| fallopian tube cancer that is located in the fallopian tube

| [http://www.disease-ontology.org/?id=DOID:1963 DOID:1963]

|

|

|

|-

| fallopian tube carcinosarcoma

| class of disease

| fallopian tube cancer

| fallopian tube cancer that is characterized as a mixture of carcinoma and sarcoma and has material basis in epithelial tissue and has material basis in connective tissue

| [http://www.disease-ontology.org/?id=DOID:1970 DOID:1970]

|

|

|

|-

| fallopian tube clear cell adenocarcinoma

| class of disease

| fallopian tube adenocarcinoma
clear cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5301 DOID:5301]

|

|

|

|-

| fallopian tube cystadenofibroma

| class of disease

| fallopian tube adenofibroma
cystadenofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8211 DOID:8211]

|

|

|

|-

| fallopian tube disease

| class of disease

| female reproductive system disease
adnexal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1962 DOID:1962]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.056.390 C13.351.500.056.390]

| Diseases and disorders of fallopian tubes

|

|-

| fallopian tube endometrioid adenocarcinoma

| class of disease

| fallopian tube adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5831 DOID:5831]

|

|

|

|-

| fallopian tube endometriosis

| class of disease

| fallopian tube disease
endometriosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:11424 DOID:11424]

|

| Endometriosis of fallopian tube

|

|-

| fallopian tube germ cell cancer

| class of disease

| fallopian tube cancer
germ cell cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5324 DOID:5324]

|

|

|

|-

| fallopian tube gestational choriocarcinoma

| class of disease

| fallopian tube carcinoma
gestational choriocarcinoma
fallopian tube germ cell cancer
familiar fallopian tube carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8186 DOID:8186]

|

|

|

|-

| fallopian tube leiomyoma

| class of disease

| fallopian tube benign neoplasm
leiomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5124 DOID:5124]

|

|

|

|-

| fallopian tube leiomyosarcoma

| class of disease

| fallopian tube cancer
leiomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1965 DOID:1965]

|

|

|

|-

| fallopian tube mucinous adenocarcinoma

| class of disease

| fallopian tube adenocarcinoma
fallopian tube mucinous tumor
mucinous adenocarcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:3704 DOID:3704]

|

|

|

|-

| fallopian tube mucinous tumor

| class of disease

| fallopian tube benign neoplasm
mucinous tumor
fallopian tube cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3705 DOID:3705]

|

|

|

|-

| fallopian tube papillary adenocarcinoma

| class of disease

| fallopian tube adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5597 DOID:5597]

|

|

|

|-

| fallopian tube serous adenocarcinoma

| class of disease

| fallopian tube adenocarcinoma
serous cystadenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5598 DOID:5598]

|

|

|

|-

| fallopian tube serous papilloma

| class of disease

| fallopian tube benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3173 DOID:3173]

|

|

|

|-

| fallopian tube squamous cell carcinoma

| class of disease

| fallopian tube carcinoma
squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5540 DOID:5540]

|

|

|

|-

| fallopian tube teratoma

| class of disease

| fallopian tube germ cell cancer
fallopian tube cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5564 DOID:5564]

|

|

|

|-

| fallopian tube transitional cell carcinoma

| class of disease

| fallopian tube carcinoma
transitional cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4008 DOID:4008]

|

|

|

|-

| familial GPIHBP1 deficiency

| class of disease

| autosomal recessive disease
familial chylomicronemia syndrome
hyperlipoproteinemia type I

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111420 DOID:0111420]

|

|

|

|-

| familial adenomatous polyposis 1

| class of disease

| familial adenomatous polyposis
autosomal dominant disease

| familial adenomatous polyposis that has material basis in heterozygous mutation in the APC gene on chromosome 5q22

| [http://www.disease-ontology.org/?id=DOID:0080409 DOID:0080409]

|

|

|

|-

| familial adenomatous polyposis 2

| class of disease

| familial adenomatous polyposis
autosomal recessive disease

| familial adenomatous polyposis that has material basis in homozygous or compound heterozygous mutation in the MUTYH gene on chromosome 1p34

| [http://www.disease-ontology.org/?id=DOID:0080410 DOID:0080410]

|

|

|

|-

| familial adenomatous polyposis 3

| class of disease

| familial adenomatous polyposis

| familial adenomatous polyposis that has material basis in homozygous or compound heterozygous mutation in the NTHL1 gene on chromosome 16p13

| [http://www.disease-ontology.org/?id=DOID:0080411 DOID:0080411]

|

|

|

|-

| familial adult myoclonic epilepsy 4

| class of disease

| myoclonic epilepsy
benign adult familial myoclonic epilepsy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111693 DOID:0111693]

|

|

|

|-

| familial adult myoclonic epilepsy 6

| class of disease

| autosomal dominant disease
benign adult familial myoclonic epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111696 DOID:0111696]

|

|

|

|-

| familial adult myoclonic epilepsy 7

| class of disease

| benign adult familial myoclonic epilepsy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111694 DOID:0111694]

|

|

|

|-

| familial bicuspid aortic valve

| class of disease

| bicuspid aortic valve
aortic valve disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080332 DOID:0080332]

|

|

|

|-

| familial chronic myelocytic leukemia-like syndrome

| class of disease

| chronic myeloid leukemia

| chronic myeloid leukemia characterized by chronic myelocytic leukemia in early infancy and absence of the BCR/ABL fusion gene (Philadelphia chromosome)

| [http://www.disease-ontology.org/?id=DOID:0060761 DOID:0060761]

|

|

|

|-

| familial chylomicronemia due to inhibition of lipoprotein lipase activity

| class of disease

| familial chylomicronemia syndrome
hyperlipoproteinemia type I

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111419 DOID:0111419]

|

|

|

|-

| familial chylomicronemia syndrome

| class of disease

| hyperlipidemia
familial hyperlipidemia
Primary hyperchylomicronemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111417 DOID:0111417]

|

|

|

|-

| familial cold autoinflammatory syndrome 1

| class of disease

| familial cold urticaria
genetic disease

| familial cold autoinflammatory syndrome characterized by autosomal dominant inheritance that has material basis in heterozygous mutation in the NLRP gene on chromosome 1q44

| [http://www.disease-ontology.org/?id=DOID:0090062 DOID:0090062]

|

|

|

|-

| familial episodic pain syndrome

| class of disease

| neuropathic pain
peripheral neuropathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111728 DOID:0111728]

|

|

|

|-

| familial episodic pain syndrome 1

| class of disease

| familial episodic pain syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111729 DOID:0111729]

|

|

|

|-

| familial episodic pain syndrome 2

| class of disease

| familial episodic pain syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111730 DOID:0111730]

|

|

|

|-

| familial episodic pain syndrome 3

| class of disease

| familial episodic pain syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111731 DOID:0111731]

|

|

|

|-

| familial erythrocytosis 1

| class of disease

| primary polycythemia
autosomal dominant disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060652 DOID:0060652]

|

|

|

|-

| familial erythrocytosis 3

| class of disease

| primary polycythemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080338 DOID:0080338]

|

|

|

|-

| familial erythrocytosis 4

| class of disease

| primary polycythemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080339 DOID:0080339]

|

|

|

|-

| familial erythrocytosis 5

| class of disease

| primary polycythemia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080290 DOID:0080290]

|

|

|

|-

| familial erythrocytosis 6

| class of disease

| primary polycythemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111632 DOID:0111632]

|

|

|

|-

| familial erythrocytosis 7

| class of disease

| primary polycythemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111631 DOID:0111631]

|

|

|

|-

| familial febrile seizures 1

| class of disease

| febrile seizures, familial

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111307 DOID:0111307]

|

|

|

|-

| familial febrile seizures 10

| class of disease

| febrile seizures, familial

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111304 DOID:0111304]

|

|

|

|-

| familial febrile seizures 11

| class of disease

| febrile seizures, familial

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111308 DOID:0111308]

|

|

|

|-

| familial febrile seizures 2

| class of disease

| febrile seizures, familial

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111310 DOID:0111310]

|

|

|

|-

| familial febrile seizures 4

| class of disease

| febrile seizures, familial

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111305 DOID:0111305]

|

|

|

|-

| familial febrile seizures 5

| class of disease

| febrile seizures, familial

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111306 DOID:0111306]

|

|

|

|-

| familial febrile seizures 6

| class of disease

| febrile seizures, familial

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111309 DOID:0111309]

|

|

|

|-

| familial febrile seizures 7

| class of disease

| febrile seizures, familial

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111311 DOID:0111311]

|

|

|

|-

| familial febrile seizures 8

| class of disease

| febrile seizures, familial

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111298 DOID:0111298]

|

|

|

|-

| familial febrile seizures 9

| class of disease

| febrile seizures, familial

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111303 DOID:0111303]

|

|

|

|-

| familial glomangioma

| class of disease

| glomangioma
rare circulatory system disease
inherited renal tumor
cardiovascular cancer
inherited soft tissue tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7996 DOID:7996]

|

|

|

|-

| familial glucocorticoid deficiency

| class of disease

| adrenal gland disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080620 DOID:0080620]

|

|

|

|-

| familial hemiplegic migraine 1

| class of disease

| familial hemiplegic migraine

| familial hemiplegic migraine that is commonly associated with cerebellar degeneration and has material basis in heterozygous mutation in CACNA1A on 19p13

| [http://www.disease-ontology.org/?id=DOID:0111181 DOID:0111181]

|

|

|

|-

| familial hemiplegic migraine 2

| class of disease

| familial hemiplegic migraine

| A familial hemiplegic migraine that has material basis in heterozygous mutation in ATP1A2 on 1q23.2.

| [http://www.disease-ontology.org/?id=DOID:0111182 DOID:0111182]

|

|

|

|-

| familial hemiplegic migraine 3

| class of disease

| familial hemiplegic migraine

| A familial hemiplegic migraine that has material basis in heterozygous mutation in SCN1A on 2q24.3.

| [http://www.disease-ontology.org/?id=DOID:0111183 DOID:0111183]

|

|

|

|-

| familial hemophagocytic lymphohistiocytosis 1

| class of disease

| familial hemophagocytic lymphohistiocytosis
genetic disease
hemophagocytic lymphohistiocytosis
autosomal recessive disease

| A hemophagocytic lymphohistiocytosis that has material basis in an autosomal recessive mutation of HPLH1 on chromosome 9q21.3-q22.

| [http://www.disease-ontology.org/?id=DOID:0110921 DOID:0110921]

|

|

|

|-

| familial hepatic adenoma

| class of disease

| autosomal recessive disease
hepatocellular adenoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111366 DOID:0111366]

|

|

|

|-

| familial hyperinsulinemic hypoglycemia 1

| class of disease

| hyperinsulinemic hypoglycemia
genetic disease

| hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of hyperinsulinemic hypoglycemia that is resistant to diazoxide treatment that has material basis in mutation in the ABCC8 gene on chromosome 11p15

| [http://www.disease-ontology.org/?id=DOID:0070219 DOID:0070219]

|

|

|

|-

| familial hyperinsulinemic hypoglycemia 2

| class of disease

| hyperinsulinemic hypoglycemia
genetic disease

| A hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of severe hyperinsulinemic hypoglycemia that is resistant to diazoxide treatment that has material basis in mutation in the KCNJ11 gene on chromosome 11p15.1.

| [http://www.disease-ontology.org/?id=DOID:0070218 DOID:0070218]

|

|

|

|-

| familial hyperinsulinemic hypoglycemia 3

| class of disease

| hyperinsulinemic hypoglycemia
genetic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070216 DOID:0070216]

|

|

|

|-

| familial hyperinsulinemic hypoglycemia 4

| class of disease

| hyperinsulinemic hypoglycemia
genetic disease

| hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of hyperinsulinemic hypoglycemia with seizures that has material basis in mutation in the HADH gene on chromosome 4q25

| [http://www.disease-ontology.org/?id=DOID:0070215 DOID:0070215]

|

|

|

|-

| familial hyperinsulinemic hypoglycemia 5

| class of disease

| hyperinsulinemic hypoglycemia
genetic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070220 DOID:0070220]

|

|

|

|-

| familial hyperinsulinemic hypoglycemia 6

| class of disease

| hyperinsulinemic hypoglycemia
genetic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070217 DOID:0070217]

|

|

|

|-

| familial hyperinsulinemic hypoglycemia 7

| class of disease

| hyperinsulinemic hypoglycemia
genetic disease

| A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of postexercise hypoglycemia with marked hyperinsulinism that has material basis in mutation in the SLC16A1 gene on chromosome 1p13.2.

| [http://www.disease-ontology.org/?id=DOID:0070214 DOID:0070214]

|

|

|

|-

| familial hyperlipidemia

| class of disease

| lipid metabolism disorder
hyperlipidemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1168 DOID:1168]

|

|

|

|-

| familial hypertrophic cardiomyopathy

| class of disease

| hypertrophic cardiomyopathy
familial cardiomyopathy

| Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions

| [http://www.disease-ontology.org/?id=DOID:0080326 DOID:0080326]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.238.100.500 C14.280.238.100.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.484.150.070.160.500 C14.280.484.150.070.160.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.160 C16.320.160]

|

|

|-

| familial hypertryptophanemia

| class of disease

| amino acid metabolic disorder
autosomal recessive disease
hypertryptophanemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111703 DOID:0111703]

|

|

|

|-

| familial hypobetalipoproteinemia 1

| class of disease

| hypobetalipoproteinemia

| hypobetalipoproteinemia that has material basis in mutation in the APOB gene on chromosome 2p24

| [http://www.disease-ontology.org/?id=DOID:0111062 DOID:0111062]

|

|

|

|-

| familial hypobetalipoproteinemia 2

| class of disease

| hypobetalipoproteinemia

| hypobetalipoproteinemia that has material basis in homozygous or compound heterozygous mutation in the ANGPTL3 gene on chromosome 1p31

| [http://www.disease-ontology.org/?id=DOID:0111061 DOID:0111061]

|

|

|

|-

| familial hypocalciuric hypercalcemia 1

| class of disease

| familial hypocalciuric hypercalcemia
genetic disease

| familial hypocalciuric hypercalcemia that has material basis in heterozygous loss-of-function mutations in the CASR gene on chromosome 3q21

| [http://www.disease-ontology.org/?id=DOID:0060700 DOID:0060700]

|

|

|

|-

| familial isolated trichomegaly

| class of disease

| Trichomegaly
eyelid disease
autosomal recessive disease

|

| [http://www.disease-ontology.org/?id=DOID:0111566 DOID:0111566]

|

|

|

|-

| familial lipase maturation factor 1 deficiency

| class of disease

| familial chylomicronemia syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111422 DOID:0111422]

|

|

|

|-

| familial lipoprotein lipase deficiency

| class of disease

| hyperlipoproteinemia type I
autosomal recessive disease
familial chylomicronemia syndrome

| familial hyperlipemia characterized by a deficiency of the enzyme lipoprotein lipase and the subsequent build up of chylomicrons and increased plasma concentration of triglycerides

| [http://www.disease-ontology.org/?id=DOID:14118 DOID:14118]

|

|

|

|-

| familial melanoma

| class of disease

| melanoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6846 DOID:6846]

|

|

|

|-

| familial meningioma

| class of disease

| meningioma
hereditary neoplastic syndromes

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4586 DOID:4586]

|

|

|

|-

| familial multiple nevi flammei

| class of disease

| capillary disease
port-wine stain

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111529 DOID:0111529]

|

|

|

|-

| familial nephrotic syndrome

| class of disease

| nephrotic syndrome
genetic disease
monogenic disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2590 DOID:2590]

|

|

|

|-

| familial partial lipodystrophy type 1

| class of disease

| familial partial lipodystrophy

| familial partial lipodystrophy characterized by loss of adipose tissue that is confined to the extremities with normal or increased fat in other areas of the body

| [http://www.disease-ontology.org/?id=DOID:0070207 DOID:0070207]

|

|

|

|-

| familial partial lipodystrophy type 2

| class of disease

| familial partial lipodystrophy
genetic disease
autosomal dominant disease

| familial partial lipodystrophy characterized by autosomal dominant inheritance of loss of subcutaneous fat from the limbs and trunk that has material basis in mutation in the LMNA gene on chromosome 1q21

| [http://www.disease-ontology.org/?id=DOID:0070202 DOID:0070202]

|

|

|

|-

| familial partial lipodystrophy type 3

| class of disease

| familial partial lipodystrophy
genetic disease
autosomal dominant disease

| familial partial lipodystrophy characterized by autosomal dominant inheritance that has material basis in mutation in the PPARG gene on chromosome 3p25

| [http://www.disease-ontology.org/?id=DOID:0070204 DOID:0070204]

|

|

|

|-

| familial partial lipodystrophy type 6

| class of disease

| familial partial lipodystrophy
genetic disease
autosomal recessive disease

| familial partial lipodystrophy characterized by autosomal recessive inheritance that has material basis in mutation in the LIPE gene on chromosome 19q13

| [http://www.disease-ontology.org/?id=DOID:0070206 DOID:0070206]

|

|

|

|-

| familial progressive hyper- and hypopigmentation

| class of disease

| autosomal dominant disease
skin disease
familial progressive hyperpigmentation

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111373 DOID:0111373]

|

|

|

|-

| familial renal oncocytoma

| class of disease

| renal oncocytoma
inherited renal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6244 DOID:6244]

|

|

|

|-

| familial renal papillary carcinoma

| class of disease

| hereditary renal cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6163 DOID:6163]

|

|

|

|-

| familial retinoblastoma

| class of disease

| retinoblastoma
hereditary neoplastic syndromes

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4648 DOID:4648]

|

|

|

|-

| familial temporal lobe epilepsy 2

| class of disease

| temporal lobe epilepsy
genetic disease
autosomal dominant disease

| A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex or partial seizures and childhood febrile seizures that has material basis in variation in the chromosome region 12q22-q23.3.

| [http://www.disease-ontology.org/?id=DOID:0060755 DOID:0060755]

|

|

|

|-

| familial temporal lobe epilepsy 3

| class of disease

| temporal lobe epilepsy
genetic disease
autosomal dominant disease

| A temporal lobe epilepsy characterized by simple or complex partial seizures often accompanied by intense feelings of deja or altered awareness and that has material basis in variation in the chromosome region 4q13.2-q21.3.

| [http://www.disease-ontology.org/?id=DOID:0060750 DOID:0060750]

|

|

|

|-

| familial temporal lobe epilepsy 4

| class of disease

| temporal lobe epilepsy
genetic disease
autosomal dominant disease

| temporal lobe epilepsy characterized by autosomal dominant inheritance of occipitotemporal lobe epilepsy and migraine with visual aura and that has material basis in variation in the chromosome region 9q21-q22

| [http://www.disease-ontology.org/?id=DOID:0060753 DOID:0060753]

|

|

|

|-

| familial temporal lobe epilepsy 6

| class of disease

| temporal lobe epilepsy
genetic disease
autosomal dominant disease

| temporal lobe epilepsy that has material basis in variation in the chromosome region 3q25-q26

| [http://www.disease-ontology.org/?id=DOID:0060749 DOID:0060749]

|

|

|

|-

| familial temporal lobe epilepsy 7

| class of disease

| temporal lobe epilepsy
genetic disease
familial partial epilepsy
autosomal dominant disease

| temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has material basis in heterozygous mutation in the RELN gene on chromosome 7q22

| [http://www.disease-ontology.org/?id=DOID:0060751 DOID:0060751]

|

|

|

|-

| familial temporal lobe epilepsy 8

| class of disease

| temporal lobe epilepsy
genetic disease
autosomal dominant disease

| temporal lobe epilepsy characterized by autosomal dominant inheritance of complex partial seizures with occasional secondary generalization and that has material basis in heterozygous mutation in the GAL gene on chromosome 11q13

| [http://www.disease-ontology.org/?id=DOID:0060754 DOID:0060754]

|

|

|

|-

| familial thyroid dyshormonogenesis

| class of disease

| congenital hypothyroidism

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112183 DOID:0112183]

|

|

|

|-

| familiar fallopian tube carcinoma

| class of disease

| fallopian tube carcinoma
inherited gynecological tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7266 DOID:7266]

|

|

|

|-

| familiar ovarian carcinoma

| class of disease

| surface epithelial-stromal tumor
ovarian cancer
carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6901 DOID:6901]

|

|

|

|-

| farmer's lung

| class of disease

| extrinsic allergic alveolitis
disease

| hypersensitivity pneumonitis

| [http://www.disease-ontology.org/?id=DOID:14453 DOID:14453]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.483.125.365 C08.381.483.125.365]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.674.055.365 C08.674.055.365]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.680.075.365 C20.543.480.680.075.365]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C24.080.365 C24.080.365]

|

|

|-

| fasciitis

| class of disease

| connective tissue disease
disease

| Inflammation process in fascia

| [http://www.disease-ontology.org/?id=DOID:9598 DOID:9598]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.321 C05.321]

| Fasciitis

|

|-

| fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 1

| class of disease

| autosomal recessive disease
fatal infantile encephalocardiomyopathy

| fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has material basis in compound heterozygous mutation in the SCO2 gene on chromosome 22q13

| [http://www.disease-ontology.org/?id=DOID:0080357 DOID:0080357]

|

|

|

|-

| fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 3

| class of disease

| autosomal recessive disease
fatal infantile encephalocardiomyopathy

| fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has material basis in homozygous mutation in the COA5 gene on chromosome 2q11

| [http://www.disease-ontology.org/?id=DOID:0080359 DOID:0080359]

|

|

|

|-

| fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 4

| class of disease

| fatal infantile encephalocardiomyopathy
autosomal recessive disease

| fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has material basis in homozygous or compound heterozygous mutation in the COA6 gene on chromosome 1q42

| [http://www.disease-ontology.org/?id=DOID:0080360 DOID:0080360]

|

|

|

|-

| fatal multiple mitochondrial dysfunctions syndrome

| class of disease

| mitochondrial disease

| mitochondrial metabolism disease that is characterized by variants in genes involved in mitochondrial energy production, resulting in impairment of energy production at more than one stage of energy metabolism

| [http://www.disease-ontology.org/?id=DOID:0070330 DOID:0070330]

|

|

|

|-

| fatty liver disease

| class of disease

| lipid storage disease
disease

| lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis

| [http://www.disease-ontology.org/?id=DOID:9452 DOID:9452]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.241 C06.552.241]

| Fatty liver

|

|-

| favism

| class of disease

| glucose-6-phosphate dehydrogenase deficiency

| glucosephosphate dehydrogenase deficiency characterized by a hemolytic reaction to consumption of broad beans

| [http://www.disease-ontology.org/?id=DOID:13628 DOID:13628]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.141.150.480.370 C15.378.071.141.150.480.370]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.141.370 C15.378.071.141.370]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.070.480.370 C16.320.070.480.370]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.723.415.341 C25.723.415.341]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.723.756.375 C25.723.756.375]

|

|

|-

| febrile neutrophilic dermatosis

| class of disease

| reactive neutrophilic dermatose
erythema
rare rheumatologic disease
other acquired skin disease
skin disease
allergy
disease

| skin disease

| [http://www.disease-ontology.org/?id=DOID:0080746 DOID:0080746]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.229.800 C17.800.229.800]

| Febrile neutrophilic dermatosis

|

|-

| febrile seizures, familial

| class of disease

| febrile seizure
encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111297 DOID:0111297]

|

|

|

|-

| feline panleukopenia

| class of disease

| parvovirus infectious disease
cat disease

| cat disease

| [http://www.disease-ontology.org/?id=DOID:3799 DOID:3799]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.256.700.363 C01.925.256.700.363]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C22.180.460 C22.180.460]

|

|

|-

| female breast axillary tail cancer

| class of disease

| female breast cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1650 DOID:1650]

|

|

|

|-

| female breast cancer

| class of disease

| breast cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050671 DOID:0050671]

|

|

|

|-

| female breast carcinoma

| class of disease

| breast carcinoma

| breast carcinoma that is manifested in the female breast

| [http://www.disease-ontology.org/?id=DOID:7843 DOID:7843]

|

|

|

|-

| female breast central part cancer

| class of disease

| female breast cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:13799 DOID:13799]

|

|

|

|-

| female breast lower-inner quadrant cancer

| class of disease

| female breast cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1649 DOID:1649]

|

|

|

|-

| female breast lower-outer quadrant cancer

| class of disease

| female breast cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13972 DOID:13972]

|

|

|

|-

| female breast upper-inner quadrant cancer

| class of disease

| female breast cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1647 DOID:1647]

|

|

|

|-

| female breast upper-outer quadrant cancer

| class of disease

| female breast cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9773 DOID:9773]

|

|

|

|-

| female infertility of uterine origin

| class of disease

| uterine disease
female infertility

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13589 DOID:13589]

|

|

|

|-

| female reproductive endometrioid cancer

| class of disease

| female reproductive organ cancer
Endometrioid tumor

| human disease

| [http://www.disease-ontology.org/?id=DOID:3001 DOID:3001]

|

|

|

|-

| female reproductive organ benign neoplasm

| class of disease

| reproductive organ benign neoplasm
female reproductive system disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060086 DOID:0060086]

|

|

|

|-

| female reproductive organ cancer

| class of disease

| female reproductive system disease
reproductive organ cancer
female reproductive system neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:120 DOID:120]

|

| Cancers of female genital organs

|

|-

| female reproductive system disease

| class of disease

| reproductive system disease
female urogenital disease

| reproductive system disease that impairs the ability to reproduce

| [http://www.disease-ontology.org/?id=DOID:229 DOID:229]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500 C13.351.500]

| Diseases and disorders of the female reproductive system

|

|-

| female stress incontinence

| class of disease

| bladder disease
stress incontinence

| Human disease

| [http://www.disease-ontology.org/?id=DOID:724 DOID:724]

|

|

|

|-

| female urethral cancer

| class of disease

| urethral cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:738 DOID:738]

|

|

|

|-

| female-restricted syndromic X-linked intellectual disability 99

| class of disease

| X-linked dominant disease
X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112025 DOID:0112025]

|

|

|

|-

| femoral cancer

| class of disease

| bone cancer
neoplasm of femur

| bone cancer that is located in the femur

| [http://www.disease-ontology.org/?id=DOID:5546 DOID:5546]

|

|

|

|-

| femoral neuropathy

| class of disease

| mononeuropathy

| mononeuropathy that is characterized by a loss of movement or sensation in parts of the legs due to damage to the femoral nerve

| [http://www.disease-ontology.org/?id=DOID:4196 DOID:4196]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.500.200 C10.668.829.500.200]

|

|

|-

| femoral vein thrombophlebitis

| class of disease

| thrombophlebitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12282 DOID:12282]

|

|

|

|-

| fetal adenoma

| class of disease

| follicular adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8102 DOID:8102]

|

|

|

|-

| fetal akinesia deformation sequence

| class of disease

| Pena-Shokeir syndrome
monogenic disease
syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111375 DOID:0111375]

|

|

|

|-

| fetal akinesia deformation sequence syndrome 1

| class of disease

| fetal akinesia deformation sequence
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111377 DOID:0111377]

|

|

|

|-

| fetal akinesia deformation sequence syndrome 2

| class of disease

| autosomal recessive disease
fetal akinesia deformation sequence

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111378 DOID:0111378]

|

|

|

|-

| fetal akinesia deformation sequence syndrome 3

| class of disease

| fetal akinesia deformation sequence
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111376 DOID:0111376]

|

|

|

|-

| fetal akinesia deformation sequence syndrome 4

| class of disease

| fetal akinesia deformation sequence
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111379 DOID:0111379]

|

|

|

|-

| fetal alcohol effects

| class of disease

| fetal alcohol spectrum disorders

| fetal alcohol spectrum disorder that results in most, but not all, of the growth deficiency and/or craniofacial features of fetal alcohol syndrome including central nervous system dysfunction due to prenatal alcohol exposure

| [http://www.disease-ontology.org/?id=DOID:0050666 DOID:0050666]

|

|

|

|-

| fetal alcohol spectrum disorders

| class of disease

| specific developmental disorder
congenital disorder
alcohol and health
disease

| group of conditions that can occur in a person whose mother drank alcohol during pregnancy

| [http://www.disease-ontology.org/?id=DOID:0050696 DOID:0050696]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.277.220 C13.703.277.220]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.300.070 C16.300.070]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.775.100.087.323 C25.775.100.087.323]

| Fetal alcohol syndrome

| File:Photo of baby with FAS.jpg

|-

| fetal alcohol syndrome

| class of disease

| fetal alcohol spectrum disorders
disease

| severe form of fetal alcohol spectrum disorder

| [http://www.disease-ontology.org/?id=DOID:0050665 DOID:0050665]

|

| Fetal alcohol syndrome

| File:FASkid.gif

|-

| fetal erythroblastosis

| class of disease

| neonatal alloimmune disease
microcytic anemia
hematological disease of fetus and newborn
Acquired hemolytic anemia
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1098 DOID:1098]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.277.060 C13.703.277.060]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.295 C15.378.295]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.300.060 C16.300.060]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.614.304 C16.614.304]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.306 C20.306]

| Hemolytic disease of the newborn

| File:1910 Erythroblastosis Fetalis.jpg

|-

| fetal nicotine spectrum disorder

| class of disease

| specific developmental disorder
health effects of tobacco
congenital disorder
drug-induced abnormality

| specific developmental disorder that is characterized by physical, behavioral and learning birth defects resulting from maternal ingestion of nicotine during pregnancy

| [http://www.disease-ontology.org/?id=DOID:0060606 DOID:0060606]

|

| Smoking and pregnancy

| File:Pregnant woman smoking outside a London hospital.jpg

|-

| fetishism

| class of disease

| paraphilia
fetishism
disease

| sexual arousal a person receives from an object or situation

| [http://www.disease-ontology.org/?id=DOID:1235 DOID:1235]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.657.350 F03.657.350]

| Sexual fetishism

| File:Martin van Maele - La Comtesse au fouet 01.jpg

|-

| fibrillary astrocytoma

| class of disease

| brain tumor
astrocytoma
diffuse astrocytoma

| astrocytoma that is characterized as a low grade astrocytoma and has material basis in neoplastic astrocytes

| [http://www.disease-ontology.org/?id=DOID:6726 DOID:6726]

|

| Fibrillary astrocytoma

|

|-

| fibroblastic liposarcoma

| class of disease

| liposarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5698 DOID:5698]

|

|

|

|-

| fibrochondrogenesis 1

| class of disease

| fibrochondrogenesis
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080672 DOID:0080672]

|

|

|

|-

| fibrochondrogenesis 2

| class of disease

| autosomal dominant disease
autosomal recessive disease
fibrochondrogenesis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080673 DOID:0080673]

|

|

|

|-

| fibroepithelial basal cell carcinoma

| class of disease

| basal-cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4291 DOID:4291]

|

|

|

|-

| fibroepithelial polyp of the anus

| class of disease

| skin tag
benign neoplasm of anus
polyp of rectum
anal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8170 DOID:8170]

|

| Anal skin tags

|

|-

| fibroepithelial polyp of urethra

| class of disease

| skin tag
urethral disease
polyp
urethral benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8108 DOID:8108]

|

|

|

|-

| fibrogenesis imperfecta ossium

| class of disease

| syndrome

| A syndrome that involves abnormality of collagen synthesis in lamellar bones, with manifestations limited to the skeleton. The initial symptom is frequently spontaneous fractures.

| [http://www.disease-ontology.org/?id=DOID:0080040 DOID:0080040]

|

|

|

|-

| fibrolamellar hepatocellular carcinoma

| class of disease

| hepatocellular carcinoma

| A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers.

| [http://www.disease-ontology.org/?id=DOID:5015 DOID:5015]

|

|

|

|-

| fibroma

| class of disease

| connective tissue benign neoplasm
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050871 DOID:0050871]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.590.340 C04.557.450.565.590.340]

| Fibromas

| File:Weiches-fibrom-augenlid.jpg

|-

| fibromyalgia

| class of disease
symptom or sign

| myositis
chronic pain
disease

| chronic disorder of unknown etiology characterized by pain, stiffness, and tenderness

| [http://www.disease-ontology.org/?id=DOID:631 DOID:631]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.324 C05.651.324]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.799.321 C05.799.321]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.491.425 C10.668.491.425]

| Fibromyalgia

| File:Fibromyalgia pain sites APS 2019.svg

|-

| fibroosseous pseudotumor of digits

| class of disease

| bone benign neoplasm
myositis ossificans

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8153 DOID:8153]

|

|

|

|-

| fibrosarcoma

| class of disease

| connective tissue neoplasm
fibroblastic tumour
sarcoma
disease

| connective tissue cancer that has material basis in fibrous connective tissue and characterized by the presence of immature proliferating fibroblasts or undifferentiated anaplastic spindle cells in a storiform pattern

| [http://www.disease-ontology.org/?id=DOID:3355 DOID:3355]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.590.350 C04.557.450.565.590.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.350 C04.557.450.795.350]

| Fibrosarcoma

| File:Malignant peripheral nerve sheath tumour - high mag.jpg

|-

| fibrosarcoma of bone

| class of disease

| osteosarcoma
fibrosarcoma
bone sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3354 DOID:3354]

|

|

|

|-

| fibrosarcomatous osteosarcoma

| class of disease

| conventional central osteosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7603 DOID:7603]

|

|

|

|-

| fibrosclerosis of breast

| class of disease

| non-proliferative fibrocystic change of the breast
benign mammary dysplasia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10353 DOID:10353]

|

|

|

|-

| fibrous dysplasia of bone

| class of disease

| bone remodeling disease
disease

| bone remodeling disease that results in the destruction of normal bone and replacing it with fibrous bone tissue

| [http://www.disease-ontology.org/?id=DOID:0080031 DOID:0080031]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.099.708.375 C05.116.099.708.375]

| Fibrous dysplasia

|

|-

| fibrous histiocytoma

| class of disease

| histiocytoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4415 DOID:4415]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.590.425.350 C04.557.450.565.590.425.350]

|

|

|-

| fibrous meningioma

| class of disease

| meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7211 DOID:7211]

|

|

|

|-

| fibrous synovial sarcoma

| class of disease

| synovial sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5484 DOID:5484]

|

|

|

|-

| fibular collateral ligament bursitis

| class of disease

| knee disorder
enthesopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9358 DOID:9358]

|

|

|

|-

| filamentary keratitis

| class of disease

| keratitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4664 DOID:4664]

|

|

|

|-

| filarial elephantiasis

| class of disease

| filariasis
skin disease
neglected tropical disease
disease

| human disease caused by parasitic worms

| [http://www.disease-ontology.org/?id=DOID:12211 DOID:12211]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.496.490 C15.604.496.490]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.610.335.508.700.750.361.350 C01.610.335.508.700.750.361.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.920.750 C01.920.750]

| Lymphatic filariasis

| File:Elephantiasis.jpg

|-

| finger agnosia

| class of disease

| agnosia
autotopagnosia

| agnosia that is a loss of the ability to distinguish the fingers on the hand

| [http://www.disease-ontology.org/?id=DOID:0060141 DOID:0060141]

|

|

|

|-

| fish allergy

| class of disease

| food allergy
seafood allergy

| food allergy triggered by fish

| [http://www.disease-ontology.org/?id=DOID:0060513 DOID:0060513]

|

|

|

|-

| fissured tongue

| class of disease

| tongue disease
disease

| benign condition characterized by deep grooves (fissures) in the dorsum of the tongue

| [http://www.disease-ontology.org/?id=DOID:11514 DOID:11514]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.910.708 C07.465.910.708]

| Fissured tongue

| File:Fissured geographic tongue.jpg

|-

| flat ductal epithelial atypia

| class of disease

| breast intraductal proliferative lesion

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6841 DOID:6841]

|

|

|

|-

| flat retinoschisis

| class of disease

| retinoschisis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8464 DOID:8464]

|

|

|

|-

| flavivirus infectious disease

| class of disease

| Flaviviridae infectious disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:993 DOID:993]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.782.350.250 C01.925.782.350.250]

| Flavivirus infections

|

|-

| focal chorioretinitis

| class of disease

| chorioretinitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1979 DOID:1979]

|

|

|

|-

| focal dystonia

| class of disease

| dystonia
movement disorders
disease

| dystonia that is localized to a specific part of the body

| [http://www.disease-ontology.org/?id=DOID:0050836 DOID:0050836]

|

|

|

|-

| focal embolic glomerulonephritis

| class of disease

| glomerulonephritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4779 DOID:4779]

|

|

|

|-

| focal epilepsy

| class of disease

| seizure
epilepsy
disease

| epilepsy syndrome characterised by seizures preceded by isolated disturbances of a cerebral function

| [http://www.disease-ontology.org/?id=DOID:2234 DOID:2234]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490.360 C10.228.140.490.360]

|

|

|-

| focal hand dystonia

| class of disease

| focal dystonia
occupational disease

| focal dystonia that affects a single muscle or small group of muscles in the hand resulting from involuntary muscular contractions

| [http://www.disease-ontology.org/?id=DOID:0050841 DOID:0050841]

|

|

|

|-

| focal labyrinthitis

| class of disease

| labyrinthitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13867 DOID:13867]

|

|

|

|-

| focal nonepidermolytic palmoplantar keratoderma

| class of disease

| nonepidermolytic palmoplantar keratoderma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111708 DOID:0111708]

|

|

|

|-

| focal nonepidermolytic palmoplantar keratoderma 1

| class of disease

| focal nonepidermolytic palmoplantar keratoderma
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111709 DOID:0111709]

|

|

|

|-

| focal nonepidermolytic palmoplantar keratoderma 2

| class of disease

| autosomal dominant disease
focal nonepidermolytic palmoplantar keratoderma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111711 DOID:0111711]

|

|

|

|-

| focal or diffuse nonepidermolytic palmoplantar keratoderma

| class of disease

| autosomal dominant disease
nonepidermolytic palmoplantar keratoderma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111710 DOID:0111710]

|

|

|

|-

| focal segmental glomerulosclerosis 1

| class of disease

| focal segmental glomerulosclerosis
genetic disease

| A focal segmental glomerulosclerosis that has material basis in an autosomal dominant mutation of ACTN4 on chromosome 19q13.2.

| [http://www.disease-ontology.org/?id=DOID:0111128 DOID:0111128]

|

|

|

|-

| folic acid deficiency anemia

| class of disease

| deficiency anemia
megaloblastic anemia
nutritional deficiency disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14026 DOID:14026]

|

|

|

|-

| follicular adenoma

| class of disease

| thyroid adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6204 DOID:6204]

|

|

|

|-

| follicular basal cell carcinoma

| class of disease

| basal-cell carcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:4295 DOID:4295]

|

|

|

|-

| follicular dendritic cell sarcoma

| class of disease

| dendritic cell sarcoma
Epstein-Barr virus-associated mesenchymal tumor

| dendritic cell sarcoma cancer that effects the follicular dendritic cells

| [http://www.disease-ontology.org/?id=DOID:6262 DOID:6262]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.227.190 C04.557.227.190]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.250.390.190 C15.604.250.390.190]

| Follicular dendritic cell sarcoma

|

|-

| follicular mucinosis

| class of disease

| mucinosis
alopecia
sebaceous gland anomaly
baldness
Cutaneous focal mucinosis
sebaceous gland disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9905 DOID:9905]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.550.550 C17.300.550.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.329.937.122.550 C17.800.329.937.122.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.794.550 C17.800.794.550]

|

|

|-

| follicular thyroid cancer

| class of disease

| thyroid carcinoma
adenocarcinoma

| thyroid carcinoma that has material basis in follicular cells

| [http://www.disease-ontology.org/?id=DOID:3962 DOID:3962]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.060 C04.557.470.200.025.060]

| Follicular thyroid carcinoma

|

|-

| folliculitis

| class of disease

| dermatitis
hair diseases
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4409 DOID:4409]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.329.500 C17.800.329.500]

| Folliculitis

| File:Isolated folliculitis.jpg

|-

| food allergy

| class of disease

| food hypersensitivity
gastrointestinal allergy
disease

| hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body's immune system

| [http://www.disease-ontology.org/?id=DOID:3044 DOID:3044]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.370 C20.543.480.370]

| Food allergy

| File:Hives on back.jpg

|-

| form agnosia

| class of disease

| agnosia
apperceptive agnosia
visual agnosia

| agnosia that is a loss of the ability to perceive a whole object while perceiving only parts of details

| [http://www.disease-ontology.org/?id=DOID:0060142 DOID:0060142]

|

|

|

|-

| formaldehyde allergic contact dermatitis

| class of disease

| allergic contact dermatitis

| allergic contact dermatitis that has allergic trigger formaldehyde

| [http://www.disease-ontology.org/?id=DOID:0040074 DOID:0040074]

|

|

|

|-

| frontal convexity meningioma

| class of disease

| cerebral convexity meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8000 DOID:8000]

|

|

|

|-

| frontal lobe epilepsy

| class of disease

| extratemporal epilepsy
focal epilepsy

| common form of epilepsy that may appear to be related to a psychiatric problem or a sleep disorder

| [http://www.disease-ontology.org/?id=DOID:3331 DOID:3331]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490.360.270 C10.228.140.490.360.270]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490.493.188 C10.228.140.490.493.188]

|

|

|-

| frontal lobe neoplasm

| class of disease

| cerebrum cancer
frontal lobe disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12016 DOID:12016]

|

|

|

|-

| frontal sinus cancer

| class of disease

| paranasal sinus cancer
frontal sinus neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1360 DOID:1360]

|

|

|

|-

| frontal sinus neoplasm

| class of disease

| paranasal sinus neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1361 DOID:1361]

|

|

|

|-

| frontal sinus squamous cell carcinoma

| class of disease

| frontal sinus cancer
squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2441 DOID:2441]

|

|

|

|-

| frontal sinusitis

| class of disease

| sinusitis
nose disease

| sinusitis which involves infection of the frontal sinuses over the eyes in the brow area. This causes pain or pressure in the frontal sinus cavity and headache over the forehead

| [http://www.disease-ontology.org/?id=DOID:10791 DOID:10791]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.460.692.752.387 C08.460.692.752.387]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.730.749.387 C08.730.749.387]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.603.692.752.387 C09.603.692.752.387]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.748.749.387 C01.748.749.387]

|

|

|-

| frontometaphyseal dysplasia 1

| class of disease

| X-linked recessive disease
frontometaphyseal dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111786 DOID:0111786]

|

|

|

|-

| frozen shoulder

| class of disease

| connective tissue disease
periarthritis humero-scapularis
capsulitis
disease

| painful human disease of uncertain origin affecting the shoulder capsule

| [http://www.disease-ontology.org/?id=DOID:14188 DOID:14188]

|

| Adhesive capsulitis of the shoulder

| File:Gray327.png

|-

| fruit allergy

| class of disease

| food allergy
vegetable allergy

| type of food allergy caused by fruit

| [http://www.disease-ontology.org/?id=DOID:0060503 DOID:0060503]

|

|

|

|-

| functional diarrhea

| class of disease

| colonic disease
diarrhea
functional colonic disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11371 DOID:11371]

|

|

|

|-

| functional gastric disease

| class of disease

| stomach disease
functional gastrointestinal disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1159 DOID:1159]

|

|

|

|-

| fundus dystrophy

| class of disease

| eye disease
retinal degeneration
genetic vitreous-retinal disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:8501 DOID:8501]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.768.585.658 C11.768.585.658]

|

|

|-

| fungal esophagitis

| class of disease

| esophagitis
fungal infectious disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13147 DOID:13147]

|

|

|

|-

| fungal folliculitis

| class of disease

| tinea corporis

| fungal infection

| [http://www.disease-ontology.org/?id=DOID:13368 DOID:13368]

|

| Fungal folliculitis

|

|-

| fungal gastritis

| class of disease

| gastritis
fungal infectious disease
chronic gastritis

| gastrointestinal system infectious disease that involves inflammation of the stomach lining caused by fungal infection in immunocompromised patients

| [http://www.disease-ontology.org/?id=DOID:4034 DOID:4034]

|

|

|

|-

| fungal infectious disease

| class of disease

| infectious disease
bacterial infection and mycosis
disease

| disease caused by fungi to animals or humans

| [http://www.disease-ontology.org/?id=DOID:1564 DOID:1564]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.703 C01.150.703]

| Diseases and disorders due to fungi

| File:Pulmonary aspergillosis.jpg

|-

| funisitis

| class of disease

| connective tissue disease
chorioamnionitis

| connective tissue disease that is an inflammation of the connective tissue of the umbilical cord

| [http://www.disease-ontology.org/?id=DOID:0050698 DOID:0050698]

|

|

|

|-

| gait apraxia

| class of disease

| apraxia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4260 DOID:4260]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.404.400 C10.597.404.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.606.881.350.600 C10.597.606.881.350.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.413.400 C23.888.592.413.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.604.882.350.600 C23.888.592.604.882.350.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F01.700.875.350.600 F01.700.875.350.600]

|

|

|-

| galactose epimerase deficiency

| class of disease

| galactosemia
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111458 DOID:0111458]

|

|

|

|-

| galactose-1-phosphate uridylyltransferase deficiency

| class of disease

| galactosemia
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111459 DOID:0111459]

|

|

|

|-

| gall bladder carcinoma in situ

| class of disease

| in situ carcinoma
gallbladder disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050612 DOID:0050612]

|

|

|

|-

| gallamine allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger gallamine

| [http://www.disease-ontology.org/?id=DOID:0040078 DOID:0040078]

|

|

|

|-

| gallbladder adenocarcinoma

| class of disease

| gallbladder carcinoma
adenocarcinoma
adenocarcinoma of liver and intrahepatic biliary tract

| gallbladder carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:3500 DOID:3500]

|

| Gallbladder adenocarcinoma

|

|-

| gallbladder adenoma

| class of disease

| biliary tract neoplasm
gastrointestinal adenoma
gallbladder polyp
benign neoplasms by histologic type
gallbladder benign neoplasm
adenoma

| biliary tract neoplasm that has material basis in epithelial tissue of glandular origin located in the gallbladder

| [http://www.disease-ontology.org/?id=DOID:0050893 DOID:0050893]

|

|

|

|-

| gallbladder angiosarcoma

| class of disease

| angiosarcoma
gallbladder sarcoma
gallbladder cancer

| angiosarcoma and gallbladder sarcoma that is located in the gallbladder

| [http://www.disease-ontology.org/?id=DOID:4513 DOID:4513]

|

|

|

|-

| gallbladder benign neoplasm

| class of disease

| gallbladder neoplasm
biliary tract neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080640 DOID:0080640]

|

|

|

|-

| gallbladder cancer

| class of disease

| biliary tract cancer
gallbladder neoplasm
gallbladder disease
disease

| biliary tract cancer that is located in the gallbladder

| [http://www.disease-ontology.org/?id=DOID:3121 DOID:3121]

|

| Gallbladder cancer

|

|-

| gallbladder carcinoma

| class of disease

| gallbladder cancer
carcinoma

| gallbladder cancer that has material basis in abnormally proliferating cells derives from epithelial cells

| [http://www.disease-ontology.org/?id=DOID:4948 DOID:4948]

|

|

|

|-

| gallbladder disease

| class of disease

| gastrointestinal system disease
biliary disease
disease

| gastrointestinal system disease that is located in the gallbladder

| [http://www.disease-ontology.org/?id=DOID:0060262 DOID:0060262]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.564 C06.130.564]

| Diseases and disorders of gallbladder

|

|-

| gallbladder leiomyoma

| class of disease

| leiomyoma
gallbladder disease
gastrointestinal system benign neoplasm
benign neoplasm of gallbladder

| human disease

| [http://www.disease-ontology.org/?id=DOID:5140 DOID:5140]

|

|

|

|-

| gallbladder leiomyosarcoma

| class of disease

| gallbladder sarcoma
leiomyosarcoma
liver leiomyosarcoma
gallbladder cancer

| gallbladder sarcoma that is located in the gallbladder

| [http://www.disease-ontology.org/?id=DOID:5275 DOID:5275]

|

|

|

|-

| gallbladder lipoma

| class of disease

| biliary tract neoplasm
gallbladder disease
lipoma
liver lipoma
gallbladder benign neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:10201 DOID:10201]

|

|

|

|-

| gallbladder lymphoma

| class of disease

| gallbladder cancer
lymphoma
liver lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8135 DOID:8135]

|

|

|

|-

| gallbladder melanoma

| class of disease

| gallbladder cancer
melanoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8167 DOID:8167]

|

|

|

|-

| gallbladder mucinous carcinoma

| class of disease

| gallbladder adenocarcinoma
gallbladder carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6998 DOID:6998]

|

|

|

|-

| gallbladder papillary carcinoma

| class of disease

| gallbladder adenocarcinoma
carcinoma
gallbladder cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7221 DOID:7221]

|

|

|

|-

| gallbladder papillomatosis

| class of disease

| biliary tract neoplasm
papilloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3120 DOID:3120]

|

|

|

|-

| gallbladder pleomorphic giant cell adenocarcinoma

| class of disease

| gallbladder adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7222 DOID:7222]

|

|

|

|-

| gallbladder rhabdomyosarcoma

| class of disease

| gallbladder sarcoma
rhabdomyosarcoma
liver rhabdomyosarcoma
gallbladder cancer

| gallbladder sarcoma that is located in the gallbladder

| [http://www.disease-ontology.org/?id=DOID:4057 DOID:4057]

|

|

|

|-

| gallbladder sarcoma

| class of disease

| gallbladder cancer
sarcoma

| sarcoma that is located in the gallbladder

| [http://www.disease-ontology.org/?id=DOID:4058 DOID:4058]

|

|

|

|-

| gallbladder signet ring cell adenocarcinoma

| class of disease

| gallbladder adenocarcinoma
signet ring cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3499 DOID:3499]

|

|

|

|-

| gallbladder small cell carcinoma

| class of disease

| gallbladder carcinoma
gallbladder neuroendocrine neoplasm
liver neuroendocrine carcinoma
small cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7133 DOID:7133]

|

|

|

|-

| gallbladder squamous cell carcinoma

| class of disease

| gallbladder carcinoma
squamous cell carcinoma
squamous cell carcinoma of liver and intrahepatic biliary tract

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5535 DOID:5535]

|

|

|

|-

| gamma heavy chain disease

| class of disease

| heavy chain disease

| heavy chain disease that results from an overproduction of gamma antibody (IgG)

| [http://www.disease-ontology.org/?id=DOID:0060127 DOID:0060127]

|

|

|

|-

| gamma-amino butyric acid metabolism disorder

| class of disease

| amino acid metabolic disorder

| amino acid metabolic disorder characterized by impairment of the GABA catabolic pathway

| [http://www.disease-ontology.org/?id=DOID:0060176 DOID:0060176]

|

|

|

|-

| gangliocytoma

| class of disease

| central nervous system organ benign neoplasm
nervous system benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2426 DOID:2426]

|

|

|

|-

| ganglioglioma

| class of disease

| benign neoplasms by histologic type
central nervous system organ benign neoplasm

| cell type benign neoplasm that has material basis in glial-type cells

| [http://www.disease-ontology.org/?id=DOID:5078 DOID:5078]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.600.380.350 C04.557.465.625.600.380.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.670.380.350 C04.557.470.670.380.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.600.380.350 C04.557.580.625.600.380.350]

| Ganglioglioma

|

|-

| ganglioneuroblastoma

| class of disease

| neuroblastoma
neuroblastic tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4163 DOID:4163]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.600.590.650.550.300 C04.557.465.625.600.590.650.550.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.670.590.650.550.300 C04.557.470.670.590.650.550.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.600.590.650.550.300 C04.557.580.625.600.590.650.550.300]

| Ganglioneuroblastoma

|

|-

| ganglioneuroma

| class of disease

| autonomic nervous system benign neoplasm

| rare and benign tumor of the autonomic nerve fibers arising from neural crest sympathogonia

| [http://www.disease-ontology.org/?id=DOID:4817 DOID:4817]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.600.355 C04.557.465.625.600.355]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.670.355 C04.557.470.670.355]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.600.355 C04.557.580.625.600.355]

| Ganglioneuroma

|

|-

| gangliosidosis

| class of disease

| sphingolipidosis
rare genetic epilepsy
rare dyslipidemia
sphingolipidosis with epilepsy
autosomal recessive disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2368 DOID:2368]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.163.100.435.825.300 C10.228.140.163.100.435.825.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.189.435.825.300 C16.320.565.189.435.825.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.398.641.803.350 C16.320.565.398.641.803.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.595.554.825.300 C16.320.565.595.554.825.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.132.100.435.825.300 C18.452.132.100.435.825.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.563.641.803.350 C18.452.584.563.641.803.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.189.435.825.300 C18.452.648.189.435.825.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.398.641.803.350 C18.452.648.398.641.803.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.595.554.825.300 C18.452.648.595.554.825.300]

|

|

|-

| gangliosidosis GM3

| class of disease

| gangliosidosis GM1

| gangliosidosis that is characterized by neurodegeneration and mild skeletal changes and has material basis in mutation in the gene encoding beta-galactosidase-1

| [http://www.disease-ontology.org/?id=DOID:0080489 DOID:0080489]

|

|

|

|-

| gastric adenocarcinoma

| class of disease

| stomach carcinoma
adenocarcinoma

| stomach carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:3717 DOID:3717]

|

| Adenocarcinomas of stomach

|

|-

| gastric adenosquamous carcinoma

| class of disease

| adenosquamous carcinoma
gastric squamous cell carcinoma
squamous cell carcinoma
stomach carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5635 DOID:5635]

|

|

|

|-

| gastric antral vascular ectasia

| class of disease

| capillary disease
ectasia
vascular ectasia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2493 DOID:2493]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.280 C06.405.748.280]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.075.280 C14.907.075.280]

| Gastric antral vascular ectasia

|

|-

| gastric body carcinoma

| class of disease

| stomach carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6705 DOID:6705]

|

|

|

|-

| gastric cardia adenocarcinoma

| class of disease

| gastric adenocarcinoma
gastric cardia carcinoma
cardia cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6271 DOID:6271]

|

|

|

|-

| gastric cardia carcinoma

| class of disease

| stomach carcinoma
cardia cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6270 DOID:6270]

|

|

|

|-

| gastric diffuse adenocarcinoma

| class of disease

| gastric adenocarcinoma
diffuse type adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6217 DOID:6217]

|

|

|

|-

| gastric dilatation

| class of disease

| stomach disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3229 DOID:3229]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.300 C06.405.748.300]

|

|

|-

| gastric fundus cancer

| class of disease

| stomach cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:10538 DOID:10538]

|

|

|

|-

| gastric fundus carcinoma

| class of disease

| gastric fundus cancer
carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6700 DOID:6700]

|

|

|

|-

| gastric gastrinoma

| class of disease

| stomach cancer
gastrinoma
gastric neuroendocrine tumor, well differentiated, low or intermediate grade

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5579 DOID:5579]

|

|

|

|-

| gastric hemangioma

| class of disease

| benign neoplasm of stomach
gastrointestinal system benign neoplasm
hemangioma of intra-abdominal structure
hemangioma
stomach disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:275 DOID:275]

|

|

|

|-

| gastric leiomyoma

| class of disease

| gastrointestinal system benign neoplasm
leiomyoma
benign neoplasm of stomach

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10087 DOID:10087]

|

|

|

|-

| gastric leiomyosarcoma

| class of disease

| stomach cancer
gastrointestinal system disease
gastrointestinal system cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5280 DOID:5280]

|

|

|

|-

| gastric liposarcoma

| class of disease

| stomach cancer
gastrointestinal system disease
gastrointestinal system cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5700 DOID:5700]

|

|

|

|-

| gastric lymphoma

| class of disease

| gastrointestinal lymphoma
stomach cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10540 DOID:10540]

|

|

|

|-

| gastric mucosal hypertrophy

| class of disease

| gastritis
rare gastroesophageal disease
genetic disease
rare genetic gastroenterological disease
chronic gastritis

| human disease

| [http://www.disease-ontology.org/?id=DOID:8757 DOID:8757]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.697.410 C06.405.205.697.410]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.398.410 C06.405.748.398.410]

| Ménétrier's disease

|

|-

| gastric neuroendocrine neoplasm

| class of disease

| gastrointestinal neuroendocrine benign tumor
stomach cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4715 DOID:4715]

|

|

|

|-

| gastric outlet obstruction

| class of disease

| stomach disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3122 DOID:3122]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.340 C06.405.748.340]

| Gastric outlet obstruction

|

|-

| gastric papillary adenocarcinoma

| class of disease

| gastric adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5593 DOID:5593]

|

|

|

|-

| gastric pylorus carcinoma

| class of disease

| stomach carcinoma
pylorus cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6703 DOID:6703]

|

|

|

|-

| gastric signet ring cell adenocarcinoma

| class of disease

| gastric diffuse adenocarcinoma
signet ring cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8025 DOID:8025]

|

|

|

|-

| gastric small cell carcinoma

| class of disease

| stomach carcinoma
gastric neuroendocrine neoplasm
small cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6552 DOID:6552]

|

|

|

|-

| gastric squamous cell carcinoma

| class of disease

| stomach carcinoma
squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5516 DOID:5516]

|

|

|

|-

| gastric teratoma

| class of disease

| stomach cancer
gastrointestinal system disease
gastrointestinal system cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:5561 DOID:5561]

|

|

|

|-

| gastric tubular adenocarcinoma

| class of disease

| gastric adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6595 DOID:6595]

|

|

|

|-

| gastric ulcer

| class of disease

| peptic ulcer disease

| An ulcerated lesion in the mucosal surface of the stomach. It may progress to involve the deeper layers of the gastric wall.

| [http://www.disease-ontology.org/?id=DOID:10808 DOID:10808]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.275.800.849 C06.405.469.275.800.849]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.586.849 C06.405.748.586.849]

| Gastric ulcers

| File:Erosive gastric ulcer.jpg

|-

| gastrin secretion abnormality

| class of disease

| endocrine pancreas disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13656 DOID:13656]

|

|

|

|-

| gastrinoma

| class of disease

| neuroendocrine tumor
disease

| neuroendocrine tumor that results in an overproduction of gastric acid

| [http://www.disease-ontology.org/?id=DOID:5577 DOID:5577]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.290.500 C04.557.470.200.025.290.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.761.500.124 C04.588.274.761.500.124]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.475.500.124 C04.588.322.475.500.124]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.761.500.124 C06.301.761.500.124]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.689.667.500.124 C06.689.667.500.124]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.421.500.124 C19.344.421.500.124]

| Gastrinoma

|

|-

| gastritis

| class of disease

| stomach disease
disease

| stomach disease that is an inflammation of the lining of the stomach

| [http://www.disease-ontology.org/?id=DOID:4029 DOID:4029]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.697 C06.405.205.697]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.398 C06.405.748.398]

| Gastritis

| File:Gastritis erosiva.2278.jpg

|-

| gastroduodenal Crohn's disease

| class of disease

| Crohn's disease

| inflammatory bowel disease characterized by inflammation located in stomach and located in duodenum, has symptom nausea, has symptom vomiting, has symptom weight loss and has symptom loss of appetite

| [http://www.disease-ontology.org/?id=DOID:0060191 DOID:0060191]

|

|

|

|-

| gastroduodenitis

| class of disease

| peptic ulcer disease
hemorrhagic duodenitis
gastritis
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8644 DOID:8644]

|

|

|

|-

| gastroenteritis

| class of disease
symptom or sign

| gastrointestinal system disease
digestive sign
disease

| medical condition characterized by inflammation of the stomach and/or small intestine

| [http://www.disease-ontology.org/?id=DOID:2326 DOID:2326]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205 C06.405.205]

| Gastroenteritis

| File:Gastroenteritis viruses.jpg

|-

| gastroesophageal adenocarcinoma

| class of disease

| adenocarcinoma
gastroesophageal cancer

| gastroesophageal cancer that has material basis in abnormally proliferating cells, derives from epithelial cells, which originate in glandular tissue

| [http://www.disease-ontology.org/?id=DOID:0080375 DOID:0080375]

|

|

|

|-

| gastroesophageal cancer

| class of disease

| gastrointestinal system cancer

| gastrointestinal system cancer that is located in the proximal esophagus and the distal stomach

| [http://www.disease-ontology.org/?id=DOID:0080374 DOID:0080374]

|

|

|

|-

| gastroesophageal junction adenocarcinoma

| class of disease

| gastrointestinal carcinoma
gastroesophageal adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4944 DOID:4944]

|

|

|

|-

| gastroesophageal reflux disease

| class of disease

| genetic disease
stomach disease
esophagitis
gastrointestinal system disease
esophageal disease

| chronic disease caused by stomach acid coming up from the stomach into the esophagus

| [http://www.disease-ontology.org/?id=DOID:8534 DOID:8534]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.117.119.500.484 C06.405.117.119.500.484]

| Gastroesophageal reflux disease

| File:Peptic stricture.png

|-

| gastrointestinal adenoma

| class of disease

| gastrointestinal system cancer
adenoma
gastrointestinal system benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4147 DOID:4147]

|

|

|

|-

| gastrointestinal allergy

| class of disease

| allergy

| hypersensitivity reaction type I disease located in the gastrointestinal tract

| [http://www.disease-ontology.org/?id=DOID:0060502 DOID:0060502]

|

|

|

|-

| gastrointestinal anthrax

| class of disease

| anthrax
gastrointestinal system disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:13386 DOID:13386]

|

|

|

|-

| gastrointestinal carcinoma

| class of disease

| gastrointestinal system cancer
carcinoma

| gastrointestinal system cancer that has material basis in epithelial cells

| [http://www.disease-ontology.org/?id=DOID:0050922 DOID:0050922]

|

|

|

|-

| gastrointestinal lymphoma

| class of disease

| gastrointestinal system cancer
gastrointestinal system disease
non-Hodgkin lymphoma
lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:903 DOID:903]

|

|

|

|-

| gastrointestinal neuroendocrine benign tumor

| class of disease

| gastrointestinal system benign neoplasm
gastrointestinal system disease
gastroenteropancreatic neuroendocrine neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4148 DOID:4148]

|

|

|

|-

| gastrointestinal neuroendocrine tumor

| class of disease

| gastrointestinal neoplasm
neuroendocrine tumor
gastrointestinal system cancer

| gastrointestinal system cancer that has material basis in neuroendocrine cells

| [http://www.disease-ontology.org/?id=DOID:0050626 DOID:0050626]

|

|

|

|-

| gastrointestinal stromal tumor

| class of disease

| Stromal tumor
rare genetic intestinal disease
inherited digestive tract tumor
mesenchymal tumor of small intestine
gastrointestinal system cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:9253 DOID:9253]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.370 C04.557.450.565.370]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.371.308 C06.301.371.308]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.249.308 C06.405.249.308]

| Gastrointestinal stromal tumors

| File:GIST 2.jpg

|-

| gastrointestinal system benign neoplasm

| class of disease

| organ system benign neoplasm
gastrointestinal neoplasm
gastrointestinal system disease

| organ system benign neoplasm located in gastrointestinal tract organs

| [http://www.disease-ontology.org/?id=DOID:0050624 DOID:0050624]

|

| Benign neoplasms of gastrointestinal tract

|

|-

| gastrointestinal system cancer

| class of disease

| digestive system cancer
gastrointestinal neoplasm
organ system cancer
gastrointestinal system disease

| organ system cancer located in gastrointestinal tract that is manifested in organs of the gastrointestinal system

| [http://www.disease-ontology.org/?id=DOID:3119 DOID:3119]

|

| Gastrointestinal cancers

|

|-

| gastrointestinal system disease

| class of disease

| disease of anatomical entity
disease

| disease involving the gastrointestinal tract

| [http://www.disease-ontology.org/?id=DOID:77 DOID:77]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06 C06]

| Diseases and disorders of the digestive system

|

|-

| gastrointestinal tularemia

| class of disease

| tularemia
gastrointestinal system disease

| tularemia that results in formation of ulcerative lesions located in gastrointestinal tract

| [http://www.disease-ontology.org/?id=DOID:14239 DOID:14239]

|

|

|

|-

| gastrojejunal ulcer

| class of disease

| peptic ulcer disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10927 DOID:10927]

|

|

|

|-

| gastroparesis

| class of disease

| functional gastric disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11914 DOID:11914]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.543 C06.405.748.543]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.636.263 C23.888.592.636.263]

| Gastroparesis

| File:GastroparesisXray.jpg

|-

| geleophysic dysplasia 1

| class of disease

| geleophysic dysplasia
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111725 DOID:0111725]

|

|

|

|-

| geleophysic dysplasia 3

| class of disease

| geleophysic dysplasia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111727 DOID:0111727]

|

|

|

|-

| gemistocytic astrocytoma

| class of disease

| astrocytoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:7005 DOID:7005]

|

|

| File:Histopathology of gemistocytic astrocytoma.jpg

|-

| gender dysphoria

| class of disease

| mental disorder
dysphoria
disease

| mental distress resulting from mismatch between gender identity and biological gender assigned at birth

| [http://www.disease-ontology.org/?id=DOID:1234 DOID:1234]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.835.550 F03.835.550]

|

|

|-

| gene duplication disease

| class of disease

| monogenic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080712 DOID:0080712]

|

|

|

|-

| generalized anxiety disorder

| class of disease

| anxiety disorder
disease

| anxiety disorder that is characterized by long-lasting anxiety that is not focused on any one object or situation

| [http://www.disease-ontology.org/?id=DOID:14320 DOID:14320]

|

| Generalized anxiety disorder

|

|-

| generalized atherosclerosis

| class of disease

| atherosclerosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2347 DOID:2347]

|

|

|

|-

| generalized dystonia

| class of disease

| dystonia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050835 DOID:0050835]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.079.357 C10.228.140.079.357]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.662.300.200 C10.228.662.300.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.500.393 C10.574.500.393]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.400.330 C16.320.400.330]

|

|

|-

| generalized epidermolysis bullosa simplex

| class of disease

| epidermolysis bullosa simplex
basal epidermolysis bullosa simplex
autosomal dominant disease

| epidermolysis bullosa simplex that is characterized by widespread blisters that appear at birth or in early infancy

| [http://www.disease-ontology.org/?id=DOID:0080511 DOID:0080511]

|

|

|

|-

| generalized epilepsy

| class of disease

| epilepsy
seizure

| epilepsy syndrome that is characterised by generalised seizures with no apparent cause which arise from independent foci or epileptic circuits that involve the whole brain

| [http://www.disease-ontology.org/?id=DOID:1827 DOID:1827]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490.375 C10.228.140.490.375]

|

|

|-

| generalized epilepsy with febrile seizures plus 1

| class of disease

| generalized epilepsy with febrile seizures plus

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111302 DOID:0111302]

|

|

|

|-

| generalized epilepsy with febrile seizures plus 10

| class of disease

| generalized epilepsy with febrile seizures plus

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111296 DOID:0111296]

|

|

|

|-

| generalized epilepsy with febrile seizures plus 2

| class of disease

| generalized epilepsy with febrile seizures plus

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111294 DOID:0111294]

|

|

|

|-

| generalized epilepsy with febrile seizures plus 4

| class of disease

| generalized epilepsy with febrile seizures plus

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111293 DOID:0111293]

|

|

|

|-

| generalized epilepsy with febrile seizures plus 6

| class of disease

| generalized epilepsy with febrile seizures plus

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111300 DOID:0111300]

|

|

|

|-

| generalized epilepsy with febrile seizures plus 7

| class of disease

| generalized epilepsy with febrile seizures plus

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111295 DOID:0111295]

|

|

|

|-

| generalized epilepsy with febrile seizures plus 8

| class of disease

| generalized epilepsy with febrile seizures plus

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111299 DOID:0111299]

|

|

|

|-

| generalized epilepsy with febrile seizures plus 9

| class of disease

| generalized epilepsy with febrile seizures plus

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111301 DOID:0111301]

|

|

|

|-

| genetic disease

| class of disease

| hereditary disorder
disease

| health problem caused by one or more abnormalities in the genome

| [http://www.disease-ontology.org/?id=DOID:630 DOID:630]
[http://www.disease-ontology.org/?id=DOID:0050325 DOID:0050325]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320 C16.320]

| Genetic diseases and disorders

|

|-

| geniculate ganglionitis

| class of disease

| facial nerve disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14075 DOID:14075]

|

|

|

|-

| geniculate herpes zoster

| class of disease

| herpes zoster
poliomyelitis
facial nerve disease

| disorder that is caused by the reactivation of varicella zoster virus in the geniculate ganglion, a nerve cell bundle of the facial nerve

| [http://www.disease-ontology.org/?id=DOID:9210 DOID:9210]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.256.466.930.750.733 C01.925.256.466.930.750.733]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.299.750 C07.465.299.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.218.513 C09.218.513]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.319.750 C10.292.319.750]

| Ramsay Hunt syndrome type II

|

|-

| genital leiomyoma

| class of disease

| reproductive organ benign neoplasm
leiomyoma cutis

| human disease

| [http://www.disease-ontology.org/?id=DOID:5147 DOID:5147]

|

|

|

|-

| geographic tongue

| class of disease
symptom or sign

| inflammation
tongue disease
smooth tongue
disease

| atrophic glossitis that is characterized as an inflammatory condition of the mucous membrane of the tongue, usually on the dorsal surface

| [http://www.disease-ontology.org/?id=DOID:1455 DOID:1455]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.910.363.447 C07.465.910.363.447]

| Geographic tongue

|

|-

| germ cell and embryonal cancer

| class of disease

| germ cell cancer
sarcoma

| germ cell cancer that is derives from a mixture of germs cells and embryonal cells

| [http://www.disease-ontology.org/?id=DOID:3095 DOID:3095]

|

|

|

|-

| germ cell benign neoplasm

| class of disease

| benign neoplasms by histologic type
germ cell tumor

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080601 DOID:0080601]

|

|

|

|-

| germ cell cancer

| class of disease

| cell type cancer
germ cell tumor

| A cell type cancer that has_material_basis_in abnormally proliferating cells derived_from germ cells.

| [http://www.disease-ontology.org/?id=DOID:2994 DOID:2994]

|

| Germ cell cancers

|

|-

| germinoma

| class of disease

| germ cell cancer
disease

| germ cell cancer that lacks histologic differentiation, usually a brain tumor

| [http://www.disease-ontology.org/?id=DOID:3304 DOID:3304]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.330 C04.557.465.330]

| Germinoma

|

|-

| gestational choriocarcinoma

| class of disease

| choriocarcinoma
extragonadal non-dysgerminomatous germ cell tumor
extragonadal germ cell cancer
gestational trophoblastic disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2025 DOID:2025]

|

|

|

|-

| gestational diabetes

| class of disease

| diabetes
complication of pregnancy, childbirth and the puerperium
diabetes mellitus and pregnancy
disease

| condition in which a woman without diabetes develops high blood sugar levels during pregnancy

| [http://www.disease-ontology.org/?id=DOID:11714 DOID:11714]
[http://www.disease-ontology.org/?id=DOID:1550 DOID:1550]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.703.170 C12.050.703.170]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.394.750.448 C18.452.394.750.448]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.246.200 C19.246.200]

| Gestational diabetes

| File:Blue circle for diabetes.svg

|-

| gestational ovarian choriocarcinoma

| class of disease

| choriocarcinoma of ovary
malignant non-dysgerminomatous germ cell tumor of ovary
ovarian cancer
gestational choriocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7591 DOID:7591]

|

|

|

|-

| gestational uterine corpus choriocarcinoma

| class of disease

| gestational choriocarcinoma
uterine corpus choriocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8187 DOID:8187]

|

|

|

|-

| giant axonal neuropathy

| class of disease

| axonal neuropathy
genetic disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0090068 DOID:0090068]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.500.300.490 C10.500.300.490]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.500.495.490 C10.574.500.495.490]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.325 C10.668.829.325]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.800.300.490 C10.668.829.800.300.490]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.666.300.490 C16.131.666.300.490]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.400.375.490 C16.320.400.375.490]

|

|

|-

| giant cell glioblastoma

| class of disease

| glioblastoma

| glioblastoma multiforme that is characterized by a prevalence of bizarre, multinucleated giant cells

| [http://www.disease-ontology.org/?id=DOID:3074 DOID:3074]

|

|

|

|-

| giant cell reparative granuloma

| class of disease

| giant-cell tumor of bone

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1866 DOID:1866]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.500.368 C05.500.368]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.320.391 C07.320.391]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.258.557 C07.465.714.258.557]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.382.468 C23.550.382.468]

|

|

|-

| giant cell tumor

| class of disease

| connective tissue neoplasm
bone benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:200 DOID:200]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.380 C04.557.450.565.380]

| Giant cell tumors

|

|-

| giant hemangioma

| class of disease

| cavernous hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5774 DOID:5774]

|

|

|

|-

| giant papillary conjunctivitis

| class of disease

| blepharoconjunctivitis
papillary conjunctivitis
allergic conjunctivitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2457 DOID:2457]

|

|

|

|-

| giant-cell carcinoma of the lung

| class of disease

| large-cell lung carcinoma
Sarcomatoid carcinoma of the lung
malignant giant cell tumor

| lung carcinoma that is located in large undifferentiated cells

| [http://www.disease-ontology.org/?id=DOID:5583 DOID:5583]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.220 C04.557.470.200.220]

|

| File:Giant cell carcinoma - Case 284 (13107156794).jpg

|-

| giant-cell tumor of bone

| class of disease

| bone neoplasm
giant cell tumor
disease

| giant cell tumor and bone cancer and bone tissue neoplasm that results in the presence of multinucleated giant cells (osteoclast-like cell)

| [http://www.disease-ontology.org/?id=DOID:4305 DOID:4305]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.380.380 C04.557.450.565.380.380]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.575.420 C04.557.450.565.575.420]

| Giant-cell tumor of bone

| File:Giant cell tumour of bone - high mag.jpg

|-

| gingival disease

| class of disease

| periodontal disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1483 DOID:1483]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.258 C07.465.714.258]

|

|

|-

| gingival fibromatosis 5

| class of disease

| gingival fibromatosis
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080280 DOID:0080280]

|

|

|

|-

| gingival hypertrophy

| class of disease

| gingival overgrowth

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5338 DOID:5338]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.258.428.260 C07.465.714.258.428.260]

|

|

|-

| gingival overgrowth

| class of disease

| gingival disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3086 DOID:3086]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.258.428 C07.465.714.258.428]

| Gingival enlargement

|

|-

| gingival recession

| class of disease

| gingival disease
periodontal atrophy

| human disease

| [http://www.disease-ontology.org/?id=DOID:1134 DOID:1134]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.258.447 C07.465.714.258.447]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.354.625 C07.465.714.354.625]

| Gingival recession

|

|-

| gingivitis

| class of disease
symptom or sign

| symptom
gingival disease
periodontitis
disease

| inflammation of the gums

| [http://www.disease-ontology.org/?id=DOID:3087 DOID:3087]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.258.480 C07.465.714.258.480]

| Gingivitis

| File:Gingivitis (crop).jpg

|-

| glandular cystitis

| class of disease

| chronic cystitis

| A reactive inflammatory disorder affecting the bladder. It is characterized by the development of small cysts in the bladder wall. The cysts are lined by metaplastic glandular cells.

| [http://www.disease-ontology.org/?id=DOID:2392 DOID:2392]

|

| Cystitis glandularis

|

|-

| glandular pattern ovarian yolk sac tumor

| class of disease

| ovarian endodermal sinus tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6511 DOID:6511]

|

|

|

|-

| glandular tularemia

| class of disease

| tularemia

| tularemia that results in swelling of regional lymph glands

| [http://www.disease-ontology.org/?id=DOID:0050382 DOID:0050382]

|

|

|

|-

| glandular-alveolar pattern testicular yolk sac tumor

| class of disease

| testicular yolk sac tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7930 DOID:7930]

|

|

|

|-

| glans penis cancer

| class of disease

| penile cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11839 DOID:11839]

|

|

|

|-

| glassy cell variant cervical adenosquamous carcinoma

| class of disease

| cervical adenosquamous carcinoma

| cervical adenosquamous carcinoma that is a rare form and is composed of cells with a glass-like cytoplasm

| [http://www.disease-ontology.org/?id=DOID:8361 DOID:8361]

|

|

|

|-

| glaucoma

| class of disease

| eye disease
disease

| eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function

| [http://www.disease-ontology.org/?id=DOID:1686 DOID:1686]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.525.381 C11.525.381]

| Glaucoma

| File:Acute Angle Closure-glaucoma.jpg

|-

| glaucomatous atrophy of optic disc

| class of disease

| optic atrophy
eye degenerative disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:10337 DOID:10337]

|

|

|

|-

| glioblastoma

| class of disease

| astrocytoma
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3068 DOID:3068]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.600.380.080.335 C04.557.465.625.600.380.080.335]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.670.380.080.335 C04.557.470.670.380.080.335]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.600.380.080.335 C04.557.580.625.600.380.080.335]

| Glioblastoma

| File:Glioblastoma (1).jpg

|-

| glioblastoma classical subtype

| class of disease

| glioblastoma

| glioblastoma multiforme that is characterized by abnormally high levels of epidermal growth factor receptor and the absence of p53 mutations

| [http://www.disease-ontology.org/?id=DOID:0050803 DOID:0050803]

|

|

|

|-

| glioblastoma mesenchymal subtype

| class of disease

| glioblastoma

| glioblastoma multiforme that is characterized by the most frequent number of mutation of the Neurofibromin 1 gene

| [http://www.disease-ontology.org/?id=DOID:0050805 DOID:0050805]

|

|

|

|-

| glioblastoma neural subtype

| class of disease

| glioblastoma

| glioblastoma multiforme that is characterized by the expression of several gene types that are also typical of the brain's normal, noncancerous nerve cells, or neurons

| [http://www.disease-ontology.org/?id=DOID:0050806 DOID:0050806]

|

|

|

|-

| glioblastoma proneural subtype

| class of disease

| glioblastoma

| glioblastoma multiforme that is characterized by IDH1 and p53 mutations and Platelet Derived Growth Factor A amplification

| [http://www.disease-ontology.org/?id=DOID:0050804 DOID:0050804]

|

|

|

|-

| glioma

| class of disease

| cell type cancer
brain tumor
spinal disease
bone cancer
brain cancer
disease

| type of tumor that starts in the brain or spine

| [http://www.disease-ontology.org/?id=DOID:3070 DOID:3070]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.600.380 C04.557.465.625.600.380]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.670.380 C04.557.470.670.380]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.600.380 C04.557.580.625.600.380]

| Gliomas

| File:Glioma.gif

|-

| gliomatosis cerebri

| class of disease

| brain cancer

| rare primary brain tumor

| [http://www.disease-ontology.org/?id=DOID:6128 DOID:6128]

|

| Gliomatosis cerebri

| File:Gliomatosis cerebri.jpg

|-

| gliosarcoma

| class of disease

| glioblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3071 DOID:3071]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.600.380.400 C04.557.465.625.600.380.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.670.380.400 C04.557.470.670.380.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.600.380.400 C04.557.580.625.600.380.400]

| Gliosarcoma

|

|-

| globe disease

| class of disease

| eye disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1242 DOID:1242]

|

|

|

|-

| globoszoospermia

| class of disease

| Teratospermia
male infertility
autosomal recessive disease
spermatogenic failure

| male infertility characterized by round-headed spermatozoa lacking an acrosome

| [http://www.disease-ontology.org/?id=DOID:0111156 DOID:0111156]

|

| Globoszoospermia

| File:Globozoospermia.png

|-

| glomangioma

| class of disease

| benign perivascular tumor
glomus tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2436 DOID:2436]

|

|

|

|-

| glomangiomatosis

| class of disease

| benign perivascular tumor
glomus tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6906 DOID:6906]

|

|

|

|-

| glomangiomyoma

| class of disease

| benign perivascular tumor
glomus tumor

| human disease

| [http://www.disease-ontology.org/?id=DOID:8020 DOID:8020]

|

|

|

|-

| glomangiosarcoma

| class of disease

| glomus tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5233 DOID:5233]

|

|

|

|-

| glomeruloid hemangioma

| class of disease

| hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:486 DOID:486]

|

|

|

|-

| glomerulonephritis

| class of disease
symptom or sign

| nephritis
glomerulopathy
disease

| nephritis that causes inflammation of the glomeruli located in kidney

| [http://www.disease-ontology.org/?id=DOID:2921 DOID:2921]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.419.570.363 C12.777.419.570.363]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.419.570.363 C13.351.968.419.570.363]

| Glomerulonephritis

| File:Crescentic glomerulonephritis HE stain.JPEG

|-

| glomerulosclerosis

| class of disease

| glomerulonephritis

| glomerulonephritis that is characterized by hardening of the glomerulus in the kidney

| [http://www.disease-ontology.org/?id=DOID:0050851 DOID:0050851]

|

| Glomerulosclerosis

|

|-

| glossitis

| class of disease
symptom or sign

| tongue disease
inflammatory disease
disease

| soreness of the tongue, or more usually inflammation with depapillation of the dorsal surface of the tongue

| [http://www.disease-ontology.org/?id=DOID:1456 DOID:1456]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.910.363 C07.465.910.363]

| Glossitis

| File:Scharlach.JPG

|-

| glossopharyngeal motor neuropathy

| class of disease

| motor neuritis
glossopharyngeal nerve disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7558 DOID:7558]

|

|

|

|-

| glossopharyngeal nerve disease

| class of disease

| cranial nerve disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3418 DOID:3418]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.450 C10.292.450]

|

|

|-

| glossopharyngeal nerve paralysis

| class of disease

| glossopharyngeal nerve disease
cranial nerve palsy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3816 DOID:3816]

|

|

|

|-

| glossopharyngeal neuralgia

| class of disease

| glossopharyngeal nerve disease
neuralgia
cranial neuralgia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14423 DOID:14423]

|

|

|

|-

| glottis cancer

| class of disease

| laryngeal cancer
glottis neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2595 DOID:2595]

|

|

|

|-

| glottis carcinoma

| class of disease

| glottis cancer
carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2599 DOID:2599]

|

|

|

|-

| glottis neoplasm

| class of disease

| laryngeal neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2597 DOID:2597]

|

|

|

|-

| glucocorticoid deficiency 1

| class of disease

| familial glucocorticoid deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080621 DOID:0080621]

|

|

|

|-

| glucocorticoid-induced osteoporosis

| class of disease

| corticosteroid-induced osteoporosis
osteoporosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060343 DOID:0060343]

|

|

|

|-

| glucose intolerance

| class of disease

| hyperglycemia
disease

| pre-diabetic state of hyperglycemia that is associated with insulin resistance and increased risk of cardiovascular pathology. IGT may precede type 2 diabetes mellitus by many years

| [http://www.disease-ontology.org/?id=DOID:10603 DOID:10603]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.394.952.500 C18.452.394.952.500]

|

|

|-

| glucose metabolism disease

| class of disease

| carbohydrate metabolism disease
metabolic disease

| metabolic disorder characterized by abnormal blood glucose levels

| [http://www.disease-ontology.org/?id=DOID:4194 DOID:4194]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.394 C18.452.394]

| Glucose metabolism disorders

|

|-

| glucose-6-phosphate dehydrogenase deficiency

| class of disease

| carbohydrate metabolic disorder
disease

| carbohydrate metabolic disorder that is characterised by abnormally low levels of glucose-6-phosphate dehydrogenase (abbreviated G6PD or G6PDH)

| [http://www.disease-ontology.org/?id=DOID:2862 DOID:2862]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.141.150.480 C15.378.071.141.150.480]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.070.480 C16.320.070.480]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.202.402 C16.320.565.202.402]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.202.402 C18.452.648.202.402]

| Glucose-6-phosphate dehydrogenase deficiency

| File:G6PD - 3D structure - PDB1qki.png

|-

| glutathionuria

| class of disease

| Congenital disorders of amino acid metabolism
inborn disorder of the gamma-glutamyl cycle
amino acid metabolic disorder
autosomal recessive disease

| Gamma-glutamyl transpeptidase deficiency is characterized by increased glutathione concentration in the plasma and urine

| [http://www.disease-ontology.org/?id=DOID:0111257 DOID:0111257]

|

|

|

|-

| gluten allergy

| class of disease

| food allergy
gluten-related disorder

| allergy involving gluten

| [http://www.disease-ontology.org/?id=DOID:0060057 DOID:0060057]

|

|

|

|-

| glycogen metabolism disorder

| class of disease

| carbohydrate metabolic disorder

| carbohydrate metabolism disorder that is characterized by abnormal accumulation or depletion of liver glycogen

| [http://www.disease-ontology.org/?id=DOID:0050728 DOID:0050728]

|

|

|

|-

| glycogen storage disease

| class of disease

| glycogen metabolism disorder
overload disease
carbohydrate metabolic disorder
disease

| glycogen metabolism disorder that has material basis in enzymes deficiencies necessary in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types

| [http://www.disease-ontology.org/?id=DOID:2747 DOID:2747]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.202.449 C16.320.565.202.449]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.202.449 C18.452.648.202.449]

| Glycogen storage disease

| File:Glycogen storage disorder (PAS with diastase).jpg

|-

| glycogen storage disease IX

| class of disease

| glycogen storage disease

| glycogen storage disease characterized by deficiency of hepatic phosphorylase kinase activity

| [http://www.disease-ontology.org/?id=DOID:0050594 DOID:0050594]

|

| Glycogen storage disease type IX

|

|-

| glycogen-rich clear cell breast carcinoma

| class of disease

| breast adenocarcinoma
clear cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5310 DOID:5310]

|

|

|

|-

| goat milk allergy

| class of disease

| milk allergy

| milk allergy triggered by Capra hircus milk

| [http://www.disease-ontology.org/?id=DOID:0060522 DOID:0060522]

|

|

|

|-

| goiter

| class of disease

| thyroid gland disease
disease

| swelling of the thyroid gland

| [http://www.disease-ontology.org/?id=DOID:12176 DOID:12176]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.874.283 C19.874.283]

| Goiters

| File:Kone med stor struma.jpg

|-

| gonadal disease

| class of disease

| endocrine system disease

| endocrine system disease that is located in the gonads

| [http://www.disease-ontology.org/?id=DOID:2277 DOID:2277]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391 C19.391]

| Diseases and disorders of gonads

|

|-

| gonadal dysgenesis

| class of disease

| hypogonadism
sex differentiation disease
disease

| congenital disorder of the reproductive system

| [http://www.disease-ontology.org/?id=DOID:14447 DOID:14447]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.706.316.309 C12.706.316.309]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.875.253.309 C13.351.875.253.309]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.316.309 C16.131.939.316.309]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.119.309 C19.391.119.309]

|

|

|-

| gonadoblastoma

| class of disease

| benign neoplasms by histologic type

| cell type benign neoplasm that is composed of a mixture of gonadal elements

| [http://www.disease-ontology.org/?id=DOID:3301 DOID:3301]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.420 C04.557.465.420]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.475.395 C04.557.475.395]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.706.316.096.687.500 C12.706.316.096.687.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.706.316.309.388.500 C12.706.316.309.388.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.875.253.096.687.500 C13.351.875.253.096.687.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.875.253.309.388.500 C13.351.875.253.309.388.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.316.096.687.500 C16.131.939.316.096.687.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.316.309.388.500 C16.131.939.316.309.388.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.119.096.687.500 C19.391.119.096.687.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.119.309.388.500 C19.391.119.309.388.500]

| Gonadoblastoma

|

|-

| gonococcal bursitis

| class of disease

| bursitis
gonococcal infectious diseases

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13453 DOID:13453]

|

|

|

|-

| gonococcal seminal vesiculitis

| class of disease

| vesiculitis
gonorrhea

| human disease

| [http://www.disease-ontology.org/?id=DOID:10400 DOID:10400]

|

|

|

|-

| gonococcal spondylitis

| class of disease

| spondylitis
gonorrhea

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13127 DOID:13127]

|

|

|

|-

| gonococcal synovitis

| class of disease

| synovitis
gonococcal infectious diseases

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13454 DOID:13454]

|

|

|

|-

| gout

| class of disease
symptom or sign

| arthritis
genetic disease
crystal arthropathy
metabolic disease
disease

| medical condition that results in recurrent pain and swelling of joints

| [http://www.disease-ontology.org/?id=DOID:13189 DOID:13189]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.550.114.423 C05.550.114.423]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.550.354.500 C05.550.354.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.799.414 C05.799.414]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.798.368 C16.320.565.798.368]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.798.368 C18.452.648.798.368]

| Gout

| File:Gout2010.JPG

|-

| granular cell carcinoma

| class of disease

| carcinoma

| carcinoma that derives from epithelial cells, with polygonal accumulation of secondary lysosomes in the cytoplasm

| [http://www.disease-ontology.org/?id=DOID:4903 DOID:4903]

|

|

|

|-

| granular cell leiomyosarcoma

| class of disease

| leiomyosarcoma
rare nervous system tumor
malignant granular cell myoblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5258 DOID:5258]

|

|

|

|-

| granular cell tumor

| class of disease

| skin benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2411 DOID:2411]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.590.350 C04.557.450.590.350]

| Granular cell tumor

| File:Granular cell tumor Case 174 (5600864519).jpg

|-

| granuloma annulare

| class of disease

| dermatitis
necrobiotic disorders

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3777 DOID:3777]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.200.495.380 C17.300.200.495.380]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.550.380 C17.800.550.380]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.382.375 C23.550.382.375]

| Granuloma annulare

| File:Granuloma annulare.jpg

|-

| granulomatous amebic encephalitis

| class of disease

| Balamuthia infection
acanthamoebiasis
primary amebic meningoencephalitis
encephalopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050246 DOID:0050246]

|

| Granulomatous amoebic encephalitis

|

|-

| granulomatous angiitis

| class of disease

| vasculitis
central nervous system vasculitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2555 DOID:2555]

|

|

|

|-

| granulomatous dermatitis

| class of disease

| dermatitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4397 DOID:4397]

|

|

|

|-

| granulomatous endometritis

| class of disease

| endometritis
chronic endometritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4561 DOID:4561]

|

|

|

|-

| granulomatous gastritis

| class of disease

| gastritis
chronic gastritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4038 DOID:4038]

|

|

|

|-

| granulomatous hepatitis

| class of disease

| hepatitis
hepatic granuloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2239 DOID:2239]

|

|

|

|-

| granulomatous myositis

| class of disease

| myositis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3428 DOID:3428]

|

|

|

|-

| granulomatous orchitis

| class of disease

| testicular disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3089 DOID:3089]

|

|

|

|-

| granulosa cell tumour

| class of disease

| ovarian cancer
sex cord-gonadal stromal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2999 DOID:2999]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.475.750.656 C04.557.475.750.656]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.455.398 C04.588.322.455.398]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.056.630.705.398 C13.351.500.056.630.705.398]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.937.418.685.398 C13.351.937.418.685.398]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.410.398 C19.344.410.398]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.630.705.398 C19.391.630.705.398]

| Granulosa cell tumors

|

|-

| gray zone lymphoma

| class of disease

| lymphoma

| lymphoma that is characterized by having cellular features of both classic Hodgkin's lymphomas and large B-cell Lymphomas

| [http://www.disease-ontology.org/?id=DOID:5822 DOID:5822]

|

|

|

|-

| green color blindness

| class of disease

| dichromatopsia
deuteranopia

| human disease

| [http://www.disease-ontology.org/?id=DOID:13909 DOID:13909]

|

|

|

|-

| green mud crab allergy

| class of disease

| crustacean allergy

| crustacean allergy triggered by Scylla paramamosain

| [http://www.disease-ontology.org/?id=DOID:0060526 DOID:0060526]

|

|

|

|-

| growth hormone insensitivity syndrome with immune dysregulation 2

| class of disease

| syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080837 DOID:0080837]

|

|

|

|-

| growth hormone secreting pituitary adenoma 2

| class of disease

| growth hormone secreting pituitary adenoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112007 DOID:0112007]

|

|

|

|-

| gynatresia

| class of disease

| female reproductive system disease
atresia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:429 DOID:429]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.320 C13.351.500.320]

|

|

|-

| gynecomastia

| class of disease

| sex differentiation disease

| human disorder, which causes the appearance of breasts in males

| [http://www.disease-ontology.org/?id=DOID:12698 DOID:12698]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.090.875 C17.800.090.875]

| Gynecomastia

|

|-

| gyrate atrophy of the choroid

| class of disease

| disease
choroid disease
central gyrate choroidal dystrophy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1415 DOID:1415]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.270.468 C11.270.468]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.160.578 C11.941.160.578]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.290.468 C16.320.290.468]

|

|

|-

| haemophilus meningitis

| class of disease

| bacterial meningitis
Haemophilus influenzae infectious disease

| bacterial meningitis that has material basis in Haemophilus influenzae infection

| [http://www.disease-ontology.org/?id=DOID:0080179 DOID:0080179]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.223.500.425 C01.150.252.223.500.425]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.400.700.433.615 C01.150.252.400.700.433.615]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.228.180.500.425 C10.228.228.180.500.425]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.586.625.280.393 C10.586.625.280.393]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.207.180.500.425 C01.207.180.500.425]

|

|

|-

| hair diseases

| class of disease

| integumentary system disease

| integumentary system disease that is located in hair

| [http://www.disease-ontology.org/?id=DOID:421 DOID:421]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.329 C17.800.329]

|

|

|-

| hair follicle neoplasm

| class of disease

| skin benign neoplasm
hair diseases

| skin tumor derived from the hair matrix

| [http://www.disease-ontology.org/?id=DOID:5375 DOID:5375]

|

|

|

|-

| hairy cell leukemia

| class of disease

| chronic lymphocytic leukemia
B-cell leukemia
disease

| chronic lymphocytic leukemia that is characterized by over production of B cells (lymphocytes) by the bone marrow where the B cells appear hairy under a microscope

| [http://www.disease-ontology.org/?id=DOID:285 DOID:285]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.415 C04.557.337.415]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.553 C15.604.515.553]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.517 C20.683.515.517]

| Hairy cell leukemia

|

|-

| hairy tongue

| class of disease

| tongue disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13500 DOID:13500]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.910.791 C07.465.910.791]

| Black hairy tongue

| File:Black tongue.jpg

|-

| hallucinogen abuse

| class of disease

| substance abuse

| substance abuse that involves the recurring use of hallucinogenic drugs despite negative consequences

| [http://www.disease-ontology.org/?id=DOID:12797 DOID:12797]

|

|

|

|-

| hallucinogen dependence

| class of disease

| substance dependence
hallucinogen abuse

| drug dependence that involves the continued use of hallucinogenic drugs despite problems related to use of the substance

| [http://www.disease-ontology.org/?id=DOID:9977 DOID:9977]

|

|

|

|-

| hand dermatosis

| class of disease

| skin disease

| disease class

| [http://www.disease-ontology.org/?id=DOID:3158 DOID:3158]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.338 C17.800.338]

|

|

|-

| head and neck cancer

| class of disease

| organ system cancer
head and neck neoplasms
respiratory system cancer
disease

| organ system cancer in the head or neck region

| [http://www.disease-ontology.org/?id=DOID:11934 DOID:11934]
[http://www.disease-ontology.org/?id=DOID:3680 DOID:3680]

|

| Head and neck cancer

| File:PET-CT scanning of lymph node metastases in cancer 2.jpg

|-

| head and neck carcinoma

| class of disease

| head and neck cancer
carcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:1542 DOID:1542]

|

|

|

|-

| heart cancer

| class of disease

| cardiovascular cancer
Primary tumors of the heart
heart disease
thoracic cancer

| cardiovascular cancer located in the heart

| [http://www.disease-ontology.org/?id=DOID:117 DOID:117]

|

| Heart cancer

| File:Myxoma.jpg

|-

| heart disease

| class of disease

| cardiovascular disease

| cardiovascular system disease that involves the heart

| [http://www.disease-ontology.org/?id=DOID:114 DOID:114]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280 C14.280]

| Diseases and disorders of the heart

|

|-

| heart fibrosarcoma

| class of disease

| heart sarcoma
fibrosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6033 DOID:6033]

|

|

|

|-

| heart leiomyosarcoma

| class of disease

| heart sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5261 DOID:5261]

|

|

|

|-

| heart lipoma

| class of disease

| cardiovascular organ benign neoplasm
Primary tumors of the heart
heart disease
benign neoplasm of heart
lipoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6285 DOID:6285]

|

|

|

|-

| heart lymphoma

| class of disease

| heart cancer
lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6547 DOID:6547]

|

|

|

|-

| heart malignant hemangiopericytoma

| class of disease

| heart sarcoma
hemangiopericytoma

| heart sarcoma that is a soft tissue sarcoma located in the heart

| [http://www.disease-ontology.org/?id=DOID:6034 DOID:6034]

|

|

|

|-

| heart sarcoma

| class of disease

| heart cancer

| sarcoma and malignant neoplasm of heart that is located in the heart

| [http://www.disease-ontology.org/?id=DOID:5262 DOID:5262]

|

|

|

|-

| heart septal defect

| class of disease

| congenital heart disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1681 DOID:1681]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.240.400.560 C14.240.400.560]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.400.560 C14.280.400.560]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.240.400.560 C16.131.240.400.560]

| Heart septal defects

|

|-

| heart valve disease

| class of disease

| heart disease
disease

| disease in the valves of the heart

| [http://www.disease-ontology.org/?id=DOID:4079 DOID:4079]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.484 C14.280.484]

| Diseases and disorders of the heart valves

|

|-

| heavy chain disease

| class of disease

| type IV hypersensitivity

| hypersensitivity reaction type IV disease that results from a proliferation of cells producing immunoglobulin heavy chains

| [http://www.disease-ontology.org/?id=DOID:0060125 DOID:0060125]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.147.780.490 C15.378.147.780.490]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.435 C15.604.515.435]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.780.490 C20.683.780.490]

|

|

|-

| hemangioblastoma

| class of disease

| hemangioma
rare nervous system tumor
disease

| tumor of the central nervous system that originates from the vascular system

| [http://www.disease-ontology.org/?id=DOID:5241 DOID:5241]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.645.375.380.370 C04.557.645.375.380.370]

| Hemangioblastomas

| File:Hemangioblastoma cerebellum.jpg

|-

| hemangioma

| class of disease

| angioma
vascular neoplasm
cardiovascular organ benign neoplasm
benign neoplasms by histologic type
vascular disease
disease

| cell type benign neoplasm that has physical basis in endothelial cells that line blood vessels

| [http://www.disease-ontology.org/?id=DOID:255 DOID:255]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.645.375 C04.557.645.375]

| Skin hemangioma

| File:Capillary haemangioma.jpg

|-

| hemangioma of intra-abdominal structure

| class of disease

| hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:254 DOID:254]

|

|

|

|-

| hemangioma of lung

| class of disease

| hemangioma
lung benign neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:490 DOID:490]

|

|

|

|-

| hemangioma of orbit

| class of disease

| orbital disease
hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14459 DOID:14459]

|

|

|

|-

| hemangioma of peripheral nerve

| class of disease

| hemangioma
peripheral nervous system benign neoplasm
peripheral neuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:482 DOID:482]

|

|

|

|-

| hemangioma of spleen

| class of disease

| splenic disease
hemangioma of intra-abdominal structure

| Human disease

| [http://www.disease-ontology.org/?id=DOID:256 DOID:256]

|

|

|

|-

| hemangioma of subcutaneous tissue

| class of disease

| skin hemangioma
subcutaneous tissue disease
vascular skin disease
skin benign neoplasm
hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13081 DOID:13081]

|

|

|

|-

| hemangiopericytic tumor

| class of disease

| perivascular tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3850 DOID:3850]

|

|

|

|-

| hemangiopericytoma

| class of disease

| connective tissue neoplasm
hemangiopericytic tumor

| soft tissue cancer that is a soft tissue sarcoma and originates in the pericytes in the walls of capillaries

| [http://www.disease-ontology.org/?id=DOID:264 DOID:264]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.645.380 C04.557.645.380]

| Haemangiopericytoma

|

|-

| hematocele of tunica vaginalis testis

| class of disease
symptom or sign

| testicular disease
hematocele

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12332 DOID:12332]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.287 C12.294.287]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.414.817 C23.550.414.817]

| Hematocele

|

|-

| hematologic cancer

| class of disease
symptom or sign

| organ system cancer
hematopoietic system disease
tumor of hematopoietic and lymphoid tissues

| immune system cancer located in the hematological system that is characterized by uncontrolled cellular proliferation in blood, bone marrow and lymph nodes

| [http://www.disease-ontology.org/?id=DOID:2531 DOID:2531]

|

| Cancers of the lymph nodes and haematopoiesis

|

|-

| hematopoietic system disease

| class of disease

| symptom
disease of anatomical entity

| disorder which primarily affects the blood

| [http://www.disease-ontology.org/?id=DOID:74 DOID:74]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378 C15.378]

| Diseases and disorders of the blood

|

|-

| hemidystonia

| class of disease

| multifocal dystonia

| multifocal dystonia that involves the arm and leg on the same side of the body

| [http://www.disease-ontology.org/?id=DOID:0050846 DOID:0050846]

|

|

|

|-

| hemiparesis

| class of disease
symptom or sign

| paresis
paralysis
central nervous system disease
disease

| weakness of one side of the body

| [http://www.disease-ontology.org/?id=DOID:10969 DOID:10969]

|

|

|

|-

| hemochromatosis type 1

| class of disease

| HFE hereditary haemochromatosis
genetic disease

| hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the HFE gene on chromosome 6p22

| [http://www.disease-ontology.org/?id=DOID:0111029 DOID:0111029]

|

|

|

|-

| hemochromatosis type 2

| class of disease

| iron overload
HFE hereditary haemochromatosis

| hemochromatosis characterized by autosomal recessive inheritance of early onset of severe iron loading with symptoms including; hypogonadotropic hypogonadism, cardiomyopathy, arthropathy, and liver fibrosis or cirrhosis

| [http://www.disease-ontology.org/?id=DOID:0111034 DOID:0111034]

|

|

|

|-

| hemochromatosis type 2B

| class of disease

| hemochromatosis type 2
genetic disease

| hemochromatosis type 2 that has material basis in homozygous mutation in the HAMP gene on chromosome 19q13

| [http://www.disease-ontology.org/?id=DOID:0111032 DOID:0111032]

|

|

|

|-

| hemoglobin C

| class of disease

| hemoglobinopathy
congenital hemolytic anemia
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2859 DOID:2859]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.141.150.490 C15.378.071.141.150.490]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.420.463 C15.378.420.463]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.070.490 C16.320.070.490]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.365.463 C16.320.365.463]

|

|

|-

| hemoglobin D disease

| class of disease

| hemoglobinopathy
congenital hemolytic anemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5378 DOID:5378]

|

|

|

|-

| hemoglobin E

| class of disease

| hemoglobinopathy
congenital hemolytic anemia

| variant form of human hemoglobin

| [http://www.disease-ontology.org/?id=DOID:5379 DOID:5379]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=D12.776.124.400.463.375 D12.776.124.400.463.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=D12.776.422.316.762.426.375 D12.776.422.316.762.426.375]

|

|

|-

| hemoglobin H disease

| class of disease

| alpha thalassemia

| alpha thalassemia that has material basis in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other

| [http://www.disease-ontology.org/?id=DOID:0110031 DOID:0110031]

|

|

|

|-

| hemoglobinopathy

| class of disease

| congenital hemolytic anemia
genetic disease
hemolytic anemia
hemoglobin variant
disease

| genetic defect causing abnormal hemoglobin structure

| [http://www.disease-ontology.org/?id=DOID:2860 DOID:2860]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.420 C15.378.420]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.365 C16.320.365]

|

|

|-

| hemoglobinuria

| class of disease

| proteinuria
hemolytic anemia
disease

| condition in which the oxygen transport protein hemoglobin is found in abnormally high concentrations in the urine

| [http://www.disease-ontology.org/?id=DOID:582 DOID:582]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.934.734.634 C12.777.934.734.634]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.934.734.634 C13.351.968.934.734.634]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.942.750.634 C23.888.942.750.634]

|

| File:1GZX Haemoglobin.png

|-

| hemolytic-uremic syndrome

| class of disease

| kidney disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12554 DOID:12554]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.968.419.936.463 C12.050.351.968.419.936.463]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.777.419.936.463 C12.200.777.419.936.463]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.141.610 C15.378.071.141.610]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.140.855.925.500 C15.378.140.855.925.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.950.419.936.463 C12.950.419.936.463]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.243.937.925.500 C15.378.243.937.925.500]

| Hemolytic-uremic syndrome

| File:Schizocyte smear 2009-12-22.JPG

|-

| hemometra

| class of disease

| uterine disease
menstrual disorder
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9958 DOID:9958]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.852.495 C13.351.500.852.495]

| Hematometra

|

|-

| hemopericardium

| class of disease

| pericardial effusion

| pericardial effusion that results from blood in the pericardial sac

| [http://www.disease-ontology.org/?id=DOID:11482 DOID:11482]

|

| Hemopericardium

|

|-

| hemophagocytic lymphohistiocytosis

| class of disease

| lymphatic system disease
disease

| uncommon hematologic disorder seen more often in children than in adults

| [http://www.disease-ontology.org/?id=DOID:0050120 DOID:0050120]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.250.410.575 C15.604.250.410.575]

| Hemophagocytic lymphohistiocytosis

| File:Hemophagocytic syndrome - cropped - very high mag.jpg

|-

| hemophilia A

| class of disease
symptom or sign

| hemophilia
coagulation factor deficiency
X-linked recessive disease
blood coagulation disease
disease

| X-linked disease that has material basis in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged

| [http://www.disease-ontology.org/?id=DOID:12134 DOID:12134]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100.100.500 C15.378.100.100.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100.141.500 C15.378.100.141.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463.500 C15.378.463.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.099.500 C16.320.099.500]

| Hemophilia A

|

|-

| hemophilia B

| class of disease

| coagulation factor deficiency
inherited blood coagulation disease
X-linked recessive disease
blood coagulation disease
disease

| An inherited blood coagulation disease that has material basis in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait.

| [http://www.disease-ontology.org/?id=DOID:12259 DOID:12259]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100.100.510 C15.378.100.100.510]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100.141.510 C15.378.100.141.510]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463.510 C15.378.463.510]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.099.510 C16.320.099.510]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.322.235 C16.320.322.235]

| Hemophilia B

|

|-

| hemopneumothorax

| class of disease

| pneumothorax
hemothorax
disease

| medical term describing the combination of two conditions: pneumothorax, or air in the chest cavity, and hemothorax (also called hæmothorax), or blood in the chest cavity

| [http://www.disease-ontology.org/?id=DOID:2718 DOID:2718]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.528.338 C08.528.338]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.414.904.500 C23.550.414.904.500]

|

|

|-

| hemorrhagic cystitis

| class of disease

| cystitis

| Inflammation of the bladder resulting in bloody urine

| [http://www.disease-ontology.org/?id=DOID:0050859 DOID:0050859]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.968.829.495.250 C12.050.351.968.829.495.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.777.829.495.250 C12.200.777.829.495.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.950.829.495.250 C12.950.829.495.250]

|

|

|-

| hemorrhagic disease

| class of disease

| blood coagulation disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:2213 DOID:2213]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463 C15.378.463]

|

|

|-

| hemorrhoid

| class of disease

| gastrointestinal system disease
pelvic varices
anorectal disorder
anal disease
skin disease
disease

| vascular structures in the anal canal

| [http://www.disease-ontology.org/?id=DOID:9746 DOID:9746]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.860.401 C06.405.469.860.401]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.449 C14.907.449]

| Hemorrhoids

| File:Hemorrhoid.png

|-

| hemosiderosis

| class of disease

| iron overload
iron metabolism disease
disease

| iron metabolism disease that has material basis in an accumulation of hemosiderin, an iron-storage complex, resulting in iron overload

| [http://www.disease-ontology.org/?id=DOID:12119 DOID:12119]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.565.500.500 C18.452.565.500.500]

| Hemosiderosis

| File:Hemosiderin1.jpg

|-

| hepatic angiomyolipoma

| class of disease

| liver neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3317 DOID:3317]

|

|

|

|-

| hepatic flexure cancer

| class of disease

| ascending colon cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:260 DOID:260]

|

|

|

|-

| hepatic hemangioma

| class of disease

| liver neoplasm
hemangioma of intra-abdominal structure
hemangioma
hepatic vascular disease

| non-cancerous tumor of the liver

| [http://www.disease-ontology.org/?id=DOID:271 DOID:271]

|

| Liver hemangioma

|

|-

| hepatic infarction

| class of disease

| hepatic vascular disease
infarction
ischemic hepatitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13738 DOID:13738]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.289 C06.552.289]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.513.355.500 C23.550.513.355.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.717.489.500 C23.550.717.489.500]

| Hepatic infarction

|

|-

| hepatic osteogenic sarcoma

| class of disease

| extraosseous osteosarcoma
liver cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6370 DOID:6370]

|

|

|

|-

| hepatic vascular disease

| class of disease

| vascular disease
liver disease

| vascular disease that is located in the liver

| [http://www.disease-ontology.org/?id=DOID:272 DOID:272]

|

|

|

|-

| hepatic veno-occlusive disease

| class of disease

| hepatic vascular disease
vein disorder

| hepatic vascular disease that is characterized by obstruction of some of the small veins of the liver

| [http://www.disease-ontology.org/?id=DOID:0080177 DOID:0080177]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.360 C06.552.360]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.460 C14.907.460]

|

|

|-

| hepatitis

| class of disease
symptom or sign

| liver disease
inflammation
liver symptom
disease

| inflammation of the liver tissue

| [http://www.disease-ontology.org/?id=DOID:2237 DOID:2237]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.380 C06.552.380]

| Hepatitis

| File:Alcoholic hepatitis.jpg

|-

| hepatobiliary neoplasm

| class of disease

| gastrointestinal system benign neoplasm
liver and intrahepatic bile duct neoplasm

| gastrointestinal system neoplasm located in the hepatobiliary system

| [http://www.disease-ontology.org/?id=DOID:3117 DOID:3117]

|

|

|

|-

| hepatobiliary system cancer

| class of disease

| gastrointestinal system cancer
liver and intrahepatic bile duct neoplasm

| gastrointestinal system cancer that is located in the hepatobiliary system

| [http://www.disease-ontology.org/?id=DOID:0080355 DOID:0080355]

|

|

|

|-

| hepatoblastoma

| class of disease

| liver cancer
disease

| uncommon malignant liver cancer occurring in infants and children

| [http://www.disease-ontology.org/?id=DOID:687 DOID:687]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.435.380 C04.557.435.380]

| Hepatoblastoma

| File:Hepatoblastoma.jpg

|-

| hepatocellular adenoma

| class of disease

| liver neoplasm
endocrine gland cancer
benign neoplasms by histologic type
adenoma
disease

| Hepatocellular adenoma (HA) is a rare benign tumor of the liver

| [http://www.disease-ontology.org/?id=DOID:0050868 DOID:0050868]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.035.120 C04.557.470.035.120]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.623.040 C04.588.274.623.040]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.623.040 C06.301.623.040]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.697.040 C06.552.697.040]

| Hepatic adenoma

| File:Hepatic adenoma low mag.jpg

|-

| hepatocellular carcinoma

| class of disease

| liver carcinoma
disease

| liver carcinoma that has material basis in undifferentiated hepatocytes

| [http://www.disease-ontology.org/?id=DOID:684 DOID:684]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.255 C04.557.470.200.025.255]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.623.160 C04.588.274.623.160]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.623.160 C06.301.623.160]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.697.160 C06.552.697.160]

| Hepatocellular carcinoma

| File:Hepatocellular carcinoma 1.jpg

|-

| hepatocellular clear cell carcinoma

| class of disease

| hepatocellular carcinoma
clear cell carcinoma
clear cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5016 DOID:5016]

|

|

|

|-

| hepatoid adenocarcinoma

| class of disease

| adenocarcinoma

| adenocarcinoma with morphologic characteristics similar to hepatocellular carcinoma, arising from an anatomic site other than the liver

| [http://www.disease-ontology.org/?id=DOID:0060534 DOID:0060534]

|

|

|

|-

| hepatoid pattern ovarian yolk sac tumor

| class of disease

| ovarian endodermal sinus tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6512 DOID:6512]

|

|

|

|-

| hepatoid pattern testicular yolk sac tumor

| class of disease

| testicular yolk sac tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8195 DOID:8195]

|

|

|

|-

| hepatopulmonary syndrome

| class of disease

| liver disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:900 DOID:900]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.455 C06.552.455]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.385 C08.381.385]

|

|

|-

| hepatorenal syndrome

| class of disease

| acute kidney injury
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11823 DOID:11823]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.465 C06.552.465]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.419.291 C12.777.419.291]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.419.291 C13.351.968.419.291]

| Hepatorenal syndrome

|

|-

| hereditary ataxia

| class of disease

| neurodegeneration

| neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements

| [http://www.disease-ontology.org/?id=DOID:0050951 DOID:0050951]

|

|

|

|-

| hereditary Wilms' tumor

| class of disease

| nephroblastoma
inherited renal tumor

| nephroblastoma that results in either bilateral disease or a family history of Wilms' tumour

| [http://www.disease-ontology.org/?id=DOID:5183 DOID:5183]

|

|

|

|-

| hereditary alpha tryptasemia syndrome

| class of disease

| gene duplication disease
syndrome

|

| [http://www.disease-ontology.org/?id=DOID:0080714 DOID:0080714]

|

|

|

|-

| hereditary angioedema

| class of disease
symptom or sign

| angioedema
disease

| Hereditary angioedema (HAE) is a genetic disease characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain

| [http://www.disease-ontology.org/?id=DOID:14735 DOID:14735]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.079.500 C14.907.079.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.798.500.500 C16.320.798.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.862.945.066.500 C17.800.862.945.066.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.904.066.500 C20.543.480.904.066.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.673.795.500.500 C20.673.795.500.500]

| Hereditary angioedema

| File:Gezichtsoedeem.jpg

|-

| hereditary breast ovarian cancer

| class of disease

| autosomal dominant disease
hereditary neoplastic syndromes
syndrome
disease

| autosomal dominant disease characterized by the higher than normal tendency to develop breast and ovarian cancers in genetically related families

| [http://www.disease-ontology.org/?id=DOID:5683 DOID:5683]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.180.483 C04.588.180.483]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.455.431 C04.588.322.455.431]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.700.517 C04.700.517]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.056.630.705.431 C13.351.500.056.630.705.431]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.937.418.685.431 C13.351.937.418.685.431]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.700.517 C16.320.700.517]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.090.500.483 C17.800.090.500.483]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.410.431 C19.344.410.431]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.630.705.431 C19.391.630.705.431]

|

|

|-

| hereditary choroidal atrophy

| class of disease

| choroidal sclerosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:9794 DOID:9794]

|

|

|

|-

| hereditary combined deficiency of vitamin K-dependent clotting factors

| class of disease

| monogenic disease
blood coagulation disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112172 DOID:0112172]

|

|

|

|-

| hereditary conventional renal cell carcinoma

| class of disease

| hereditary renal cell carcinoma
renal clear cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7192 DOID:7192]

|

|

|

|-

| hereditary diffuse gastric cancer

| class of disease

| hereditary gastric cancer
stomach cancer
autosomal dominant disease
diffuse gastric cancer

| medical condition

| [http://www.disease-ontology.org/?id=DOID:0080764 DOID:0080764]

|

|

|

|-

| hereditary lymphedema

| class of disease

| lymphedema
Primary lymphedema
disease

| lymphedema commonly located in legs, caused by congenital abnormalities in the lymphatic system

| [http://www.disease-ontology.org/?id=DOID:0050580 DOID:0050580]

|

|

|

|-

| hereditary lymphedema I

| class of disease

| hereditary lymphedema

| hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood

| [http://www.disease-ontology.org/?id=DOID:0070212 DOID:0070212]

|

|

|

|-

| hereditary lymphedema IA

| class of disease

| hereditary lymphedema
genetic disease
autosomal dominant disease

| hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in mutation in the FLT4 gene on chromosome 5q35

| [http://www.disease-ontology.org/?id=DOID:0070210 DOID:0070210]

|

|

|

|-

| hereditary lymphedema IB

| class of disease

| hereditary lymphedema
autosomal dominant disease

| A hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in the chromosomal region 6q16.2-q22.1.

| [http://www.disease-ontology.org/?id=DOID:0070211 DOID:0070211]

|

|

|

|-

| hereditary lymphedema IC

| class of disease

| hereditary lymphedema
genetic disease
autosomal dominant disease

| hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in mutation in the GJC2 gene on chromosome 1q42

| [http://www.disease-ontology.org/?id=DOID:0070208 DOID:0070208]

|

|

|

|-

| hereditary lymphedema ID

| class of disease

| hereditary lymphedema
genetic disease
autosomal dominant disease

| hereditary lymphedema characterized by autosomal dominant inheritance that has material basis in mutation in the VEGFC gene on chromosome 4q34

| [http://www.disease-ontology.org/?id=DOID:0070209 DOID:0070209]

|

|

|

|-

| hereditary lymphedema II

| class of disease

| hereditary lymphedema
autosomal dominant disease

| hereditary lymphedema characterized by onset around puberty of chronic lymphedema particularly in the lower limbs with an apparent autosomal dominant pattern of inheritance

| [http://www.disease-ontology.org/?id=DOID:0070213 DOID:0070213]

|

|

|

|-

| hereditary mixed polyposis syndrome 1

| class of disease

| hereditary mixed polyposis syndrome
chromosomal duplication syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111685 DOID:0111685]

|

|

|

|-

| hereditary motor and sensory neuropathy

| class of disease

| congenital disorder
Sensorimotor neuropathy
peripheral neuropathy
hereditary peripheral neuropathy

| congenital disorder of nervous system

| [http://www.disease-ontology.org/?id=DOID:2477 DOID:2477]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.500.300 C10.500.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.500.495 C10.574.500.495]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.800.300 C10.668.829.800.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.666.300 C16.131.666.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.400.375 C16.320.400.375]

| Hereditary motor and sensory neuropathies

|

|-

| hereditary neutrophilia

| class of disease

| leukocyte disease
neutrophilia
rare genetic immune disease
genetic hematologic disease
genetic disease
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0090120 DOID:0090120]

|

|

|

|-

| hereditary night blindness

| class of disease

| night blindness

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8498 DOID:8498]

|

|

|

|-

| hereditary nonpolyposis colorectal cancer type 2

| class of disease

| Lynch syndrome

| A Lynch syndrome that has material basis in mutations in the MLH1 gene on chromosome 3p22.2.

| [http://www.disease-ontology.org/?id=DOID:0070274 DOID:0070274]

|

|

|

|-

| hereditary nonpolyposis colorectal cancer type 4

| class of disease

| Lynch syndrome

| Lynch syndrome that has material basis in heterozygous mutation in the PMS2 gene on chromosome 7p22

| [http://www.disease-ontology.org/?id=DOID:0070275 DOID:0070275]

|

|

|

|-

| hereditary nonpolyposis colorectal cancer type 5

| class of disease

| Lynch syndrome

| Lynch syndrome that has material basis in heterozygous mutation in the MSH6 gene on chromosome 2p16

| [http://www.disease-ontology.org/?id=DOID:0070272 DOID:0070272]

|

|

|

|-

| hereditary nonpolyposis colorectal cancer type 6

| class of disease

| Lynch syndrome

| Lynch syndrome that has material basis in heterozygous mutation in the TGFBR2 gene on chromosome 3p22

| [http://www.disease-ontology.org/?id=DOID:0070273 DOID:0070273]

|

|

|

|-

| hereditary nonpolyposis colorectal cancer type 7

| class of disease

| Lynch syndrome

| A Lynch syndrome that has material basis in mutation in the MLH3 gene on chromosome 14q24.3.

| [http://www.disease-ontology.org/?id=DOID:0070276 DOID:0070276]

|

|

|

|-

| hereditary nonpolyposis colorectal cancer type 8

| class of disease

| Lynch syndrome
chromosomal deletion syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070270 DOID:0070270]

|

|

|

|-

| hereditary papulotranslucent acrokeratoderma

| class of disease

| cholesteatoma

| keratosis of the hands and feet characterized by persistent, asymptomatic, yellowish to white papules and plaques associated with fine-textured scalp hair and an atopic diathesis

| [http://www.disease-ontology.org/?id=DOID:0060360 DOID:0060360]

|

|

|

|-

| hereditary renal cell carcinoma

| class of disease

| renal cell carcinoma
inherited renal tumor

| human disease

| [http://www.disease-ontology.org/?id=DOID:4455 DOID:4455]

|

|

|

|-

| hereditary retinal dystrophy

| class of disease

| fundus dystrophy
genetic disease
hereditary eye disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8500 DOID:8500]

|

|

|

|-

| hereditary sensory and autonomic neuropathy

| class of disease

| hereditary disorder
peripheral neuropathy

| congenital disorder of nervous system

| [http://www.disease-ontology.org/?id=DOID:0050548 DOID:0050548]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.500.250 C10.500.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.500.493 C10.574.500.493]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.800.175 C10.668.829.800.175]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.666.310 C16.131.666.310]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.400.415 C16.320.400.415]

|

|

|-

| hereditary sensory and autonomic neuropathy type 1

| class of disease

| hereditary sensory and autonomic neuropathy

| hereditary sensory neuropathy characterized by slowly progressing, prominent, predominantly distal sensory loss and autonomic disturbances with juvenile or adult onset and autosomal dominant inheritance

| [http://www.disease-ontology.org/?id=DOID:0070162 DOID:0070162]

|

|

|

|-

| hereditary sensory and autonomic neuropathy type 1A

| class of disease

| hereditary sensory and autonomic neuropathy type 1
genetic disease
autosomal dominant disease

| hereditary sensory and autonomic neuropathy type 1 characterized by onset of sensorimotor axonal neuropathy in the first or second decades of life that has material basis in heterozygous mutation in the SPTLC1 gene on chromosome 9q22

| [http://www.disease-ontology.org/?id=DOID:0070152 DOID:0070152]

|

|

|

|-

| hereditary sensory and autonomic neuropathy type 2

| class of disease

| hereditary sensory and autonomic neuropathy

| hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood

| [http://www.disease-ontology.org/?id=DOID:0070161 DOID:0070161]

|

|

|

|-

| hereditary sensory neuropathy X-linked

| class of disease

| hereditary sensory and autonomic neuropathy
X-linked recessive disease

| hereditary sensory neuropathy characterized by X-linked inheritance of slowly progressing neuropathy with onset in the first or second decade of life

| [http://www.disease-ontology.org/?id=DOID:0070159 DOID:0070159]

|

|

|

|-

| hereditary sensory neuropathy type 1B

| class of disease

| hereditary sensory and autonomic neuropathy
genetic disease
autosomal dominant disease

| hereditary sensory neuropathy characterized by axonal neuropathy with distal sensory impairment, cough, and gastroesophageal reflux that has material basis in variation in the chromosome region 3p24-p22

| [http://www.disease-ontology.org/?id=DOID:0070148 DOID:0070148]

|

|

|

|-

| hereditary spastic paraplegia 14

| class of disease

| hereditary spastic paraplegia
pure or complex autosomal recessive spastic paraplegia
autosomal recessive disease

| hereditary spastic paraplegia that has material basis in variation in the chromosome region 3q27-q28

| [http://www.disease-ontology.org/?id=DOID:0110767 DOID:0110767]

|

|

|

|-

| hereditary spastic paraplegia 16

| class of disease

| hereditary spastic paraplegia
pure or complex X-linked spastic paraplegia
X-linked recessive disease

| A hereditary spastic paraplegia that has material basis in variation in the chromosome region Xq11.2.

| [http://www.disease-ontology.org/?id=DOID:0110769 DOID:0110769]

|

|

|

|-

| hereditary spastic paraplegia 19

| class of disease

| hereditary spastic paraplegia
autosomal dominant pure spastic paraplegia
autosomal dominant disease

| hereditary spastic paraplegia that has material basis in variation in the chromosome region 9q

| [http://www.disease-ontology.org/?id=DOID:0110772 DOID:0110772]

|

|

|

|-

| hereditary spastic paraplegia 24

| class of disease

| hereditary spastic paraplegia
autosomal recessive complex spastic paraplegia
autosomal recessive disease

| hereditary spastic paraplegia that has material basis in variation in the chromosome region 13q14

| [http://www.disease-ontology.org/?id=DOID:0110775 DOID:0110775]

|

|

|

|-

| hereditary spastic paraplegia 25

| class of disease

| hereditary spastic paraplegia
autosomal recessive complex spastic paraplegia
autosomal recessive disease

| A hereditary spastic paraplegia that has material basis in variation in the chromosome region 6q23-q24.1.

| [http://www.disease-ontology.org/?id=DOID:0110776 DOID:0110776]

|

|

|

|-

| hereditary spastic paraplegia 27

| class of disease

| hereditary spastic paraplegia
autosomal recessive complex spastic paraplegia
autosomal recessive disease

| A hereditary spastic paraplegia that has material basis in variation in the chromosome region 10q22.1-q24.1.

| [http://www.disease-ontology.org/?id=DOID:0110778 DOID:0110778]

|

|

|

|-

| hereditary spastic paraplegia 29

| class of disease

| hereditary spastic paraplegia
autosomal dominant complex spastic paraplegia
autosomal dominant disease

| A hereditary spastic paraplegia that has material basis in variation in the chromosome region 1p31.1-p21.1.

| [http://www.disease-ontology.org/?id=DOID:0110780 DOID:0110780]

|

|

|

|-

| hereditary spastic paraplegia 32

| class of disease

| hereditary spastic paraplegia
autosomal recessive complex spastic paraplegia
autosomal recessive disease

| hereditary spastic paraplegia that has material basis in variation in the chromosome region 14q12-q21

| [http://www.disease-ontology.org/?id=DOID:0110783 DOID:0110783]

|

|

|

|-

| hereditary spastic paraplegia 34

| class of disease

| hereditary spastic paraplegia
X-linked pure spastic paraplegia
X-linked recessive disease

| hereditary spastic paraplegia that has material basis in variation in the chromosome region Xq24-q25

| [http://www.disease-ontology.org/?id=DOID:0110785 DOID:0110785]

|

|

|

|-

| hereditary spastic paraplegia 36

| class of disease

| hereditary spastic paraplegia
autosomal dominant complex spastic paraplegia
autosomal dominant disease

| hereditary spastic paraplegia that has material basis in variation in the chromosome region 12q23-q24

| [http://www.disease-ontology.org/?id=DOID:0110787 DOID:0110787]

|

|

|

|-

| hereditary spastic paraplegia 37

| class of disease

| hereditary spastic paraplegia
autosomal dominant pure spastic paraplegia
autosomal dominant disease

| A hereditary spastic paraplegia that has material basis in variation in the chromosome region 8p21.1-q13.3.

| [http://www.disease-ontology.org/?id=DOID:0110788 DOID:0110788]

|

|

|

|-

| hereditary spastic paraplegia 38

| class of disease

| hereditary spastic paraplegia
autosomal dominant complex spastic paraplegia
autosomal dominant disease

| hereditary spastic paraplegia that has material basis in variation in the chromosome region 4p16-p15

| [http://www.disease-ontology.org/?id=DOID:0110789 DOID:0110789]

|

|

|

|-

| hereditary spastic paraplegia 41

| class of disease

| hereditary spastic paraplegia
autosomal dominant pure spastic paraplegia
autosomal dominant disease

| A hereditary spastic paraplegia that has material basis in variation in the chromosome region 11p14.1-p11.2.

| [http://www.disease-ontology.org/?id=DOID:0110793 DOID:0110793]

|

|

|

|-

| hereditary spherocytosis

| class of disease

| congenital hemolytic anemia
spherocytosis
disease

| congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal biconcave disk shape

| [http://www.disease-ontology.org/?id=DOID:12971 DOID:12971]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.141.150.785 C15.378.071.141.150.785]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.070.785 C16.320.070.785]

| Hereditary spherocytosis

|

|-

| hereditary spherocytosis type 3

| class of disease

| hereditary spherocytosis
genetic disease
autosomal recessive disease

| A hereditary spherocytosis that has material basis in an autosomal dominant mutation of SPTA1 on chromosome 1q23.1.

| [http://www.disease-ontology.org/?id=DOID:0110918 DOID:0110918]

|

|

|

|-

| hernia of ovary and fallopian tube

| class of disease

| female reproductive system disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12735 DOID:12735]

|

|

|

|-

| heroin dependence

| class of disease

| opiate dependence

| opiate dependence that involves the continued use of heroin despite problems related to use of the substance

| [http://www.disease-ontology.org/?id=DOID:9976 DOID:9976]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.775.675.400 C25.775.675.400]

|

|

|-

| herpes gestationis

| class of disease

| vesiculobullous skin disease
dermatosis of pregnancy
pemphigoid
autoimmune skin disease
disease

| dermatosis of pregnancy

| [http://www.disease-ontology.org/?id=DOID:14482 DOID:14482]
[http://www.disease-ontology.org/?id=DOID:0040098 DOID:0040098]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.570 C13.703.570]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.865.700 C17.800.865.700]

| Gestational pemphigoid

| File:Pemphigoid gestationis - high mag.jpg

|-

| hexahydrophthalic anhydride allergic asthma

| class of disease

| allergic asthma

| allergic asthma that has allergic trigger hexahydrophthalic anhydride

| [http://www.disease-ontology.org/?id=DOID:0040051 DOID:0040051]

|

|

|

|-

| hexamethylene diisocyanate allergic asthma

| class of disease

| isocyanates allergic asthma

| allergic asthma to isocyanates that has allergic trigger hexamethylene diisocyanate

| [http://www.disease-ontology.org/?id=DOID:0040040 DOID:0040040]

|

|

|

|-

| hidradenitis

| class of disease

| sweat gland disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:2282 DOID:2282]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.946.315 C17.800.946.315]

|

|

|-

| hidradenoma

| class of disease

| sweat gland neoplasm
epithelial skin neoplasm
benign neoplasms by histologic type

| human disease

| [http://www.disease-ontology.org/?id=DOID:3896 DOID:3896]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.035.175 C04.557.470.035.175]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.550.175 C04.557.470.550.175]

| Hidradenoma

|

|-

| hidrocystoma

| class of disease

| apocrine sweat gland neoplasm
benign neoplasm of sweat gland

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3893 DOID:3893]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.035.175.375 C04.557.470.035.175.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.550.175.375 C04.557.470.550.175.375]

| Hidrocystoma

|

|-

| high pressure neurological syndrome

| class of disease

| central nervous system disease
diving disorder

| neurological and physiological disorder experienced by divers

| [http://www.disease-ontology.org/?id=DOID:3230 DOID:3230]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.566 C10.228.566]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C24.410 C24.410]

|

|

|-

| hilar lung carcinoma

| class of disease

| lung carcinoma
lung hilum cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8207 DOID:8207]

|

|

|

|-

| hilar lung neoplasm

| class of disease

| lung benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5767 DOID:5767]

|

|

|

|-

| histidine metabolism disease

| class of disease

| amino acid metabolic disorder

| amino acid metabolic disorder that involves deficiency in histidine

| [http://www.disease-ontology.org/?id=DOID:9265 DOID:9265]

|

|

|

|-

| histidinemia

| class of disease

| histidine metabolism disease

| histidine metabolism disease that involves a deficiency of the enzyme histidase

| [http://www.disease-ontology.org/?id=DOID:0060168 DOID:0060168]

|

|

| File:L-histidine-skeletal.png

|-

| histiocytic and dendritic cell cancer

| class of disease

| hematologic cancer
lymphoid hemopathy

| sarcoma and hematologic cancer that derives from follicular lymphoma

| [http://www.disease-ontology.org/?id=DOID:5621 DOID:5621]

|

|

|

|-

| histiocytoid hemangioma

| class of disease

| hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:474 DOID:474]

|

|

|

|-

| histiocytoma

| class of disease

| connective tissue neoplasm
connective tissue benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4231 DOID:4231]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.590.425 C04.557.450.565.590.425]

| Histiocytoma

|

|-

| histiocytosis

| class of disease

| lymphatic system disease
disease

| lymphatic system disease that is characterized by an excessive number of histiocytes

| [http://www.disease-ontology.org/?id=DOID:3405 DOID:3405]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.250 C15.604.250]

| Histiocytoses

|

|-

| histoplasmosis

| class of disease

| primary systemic mycosis
genetic disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1731 DOID:1731]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.703.450 C01.150.703.450]

| Histoplasmosis

| File:Histoplasmosis capsulatum.jpg

|-

| histoplasmosis meningitis

| class of disease

| fungal meningitis
histoplasmosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12246 DOID:12246]

|

|

|

|-

| histoplasmosis retinitis

| class of disease

| retinitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11316 DOID:11316]

|

| Presumed ocular histoplasmosis syndrome

|

|-

| histrionic personality disorder

| class of disease

| personality disorder
disease

| personality disorder characterized by excessive emotionality and attention-seeking

| [http://www.disease-ontology.org/?id=DOID:334 DOID:334]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.675.400 F03.675.400]

| Histrionic personality disorder

|

|-

| hole retinal cyst

| class of disease

| degeneration of macula and posterior pole
retinoschisis and retinal cysts
retinal perforation

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13214 DOID:13214]

|

|

|

|-

| holoprosencephaly

| class of disease
symptom or sign

| nervous system malformations
syndrome
disease

| congenital disorder of the nervous system

| [http://www.disease-ontology.org/?id=DOID:4621 DOID:4621]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.660.207.410 C05.660.207.410]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.500.034.875 C10.500.034.875]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.077.410 C16.131.077.410]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.260.380 C16.131.260.380]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.621.207.410 C16.131.621.207.410]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.666.034.875 C16.131.666.034.875]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.180.380 C16.320.180.380]

| Holoprosencephaly

| File:Alobar holoprosencephaly.jpg

|-

| holoprosencephaly 1

| class of disease

| holoprosencephaly
genetic disease
autosomal dominant disease

| A holoprosencephaly that has material basis in variation in the chromosome region 21q22.3.

| [http://www.disease-ontology.org/?id=DOID:0110881 DOID:0110881]

|

|

|

|-

| holoprosencephaly 2

| class of disease

| holoprosencephaly
genetic disease
autosomal dominant disease

| holoprosencephaly that has material basis in mutation in the homeobox-containing SIX3 gene on chromosome 2p21

| [http://www.disease-ontology.org/?id=DOID:0110872 DOID:0110872]

|

|

|

|-

| holoprosencephaly 5

| class of disease

| holoprosencephaly
genetic disease
autosomal dominant disease

| holoprosencephaly that has material basis in heterozygous mutation in the ZIC2 gene on chromosome 13q32

| [http://www.disease-ontology.org/?id=DOID:0110878 DOID:0110878]

|

|

|

|-

| holoprosencephaly 6

| class of disease

| holoprosencephaly
genetic disease

| A holoprosencephaly that has material basis in variation in the chromosome region 2q37.1-q37.3.

| [http://www.disease-ontology.org/?id=DOID:0110874 DOID:0110874]

|

|

|

|-

| holoprosencephaly 8

| class of disease

| holoprosencephaly
genetic disease

| holoprosencephaly that has material basis in variation in the chromosome region 14q13

| [http://www.disease-ontology.org/?id=DOID:0110879 DOID:0110879]

|

|

|

|-

| holoprosencephaly 9

| class of disease

| holoprosencephaly
genetic disease
autosomal dominant disease

| holoprosencephaly that has material basis in heterozygous mutation in the GLI2 gene on chromosome 2q14

| [http://www.disease-ontology.org/?id=DOID:0110873 DOID:0110873]

|

|

|

|-

| homocarnosinosis

| class of disease

| gamma-amino butyric acid metabolism disorder
inborn disorder of peptide metabolism
encephalopathy

| gamma-amino butyric acid metabolism disorder that is characterized by an excess of homocarnosine in the brain and has material basis in a deficiency of serum carnosinase in its ability to hydrolyze homocarnosine

| [http://www.disease-ontology.org/?id=DOID:0060177 DOID:0060177]

|

|

|

|-

| hordeolum

| class of disease
symptom or sign

| blepharitis
eyelid disease
disease

| bacterial infection of an oil gland in the eyelid

| [http://www.disease-ontology.org/?id=DOID:9909 DOID:9909]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.289.400 C01.150.252.289.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.375.354.400 C01.375.354.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.294.354.400 C11.294.354.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.338.648 C11.338.648]

| Stye

| File:Stye02.jpg

|-

| hordeolum externum

| class of disease

| blepharitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:13134 DOID:13134]

|

|

|

|-

| horned turban snail allergy

| class of disease

| snail allergy

| snail allergy triggered by Turbo cornutus

| [http://www.disease-ontology.org/?id=DOID:0060531 DOID:0060531]

|

|

|

|-

| human cytomegalovirus infection

| class of disease

| viral infectious disease
cytomegaloviral disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080827 DOID:0080827]

|

|

|

|-

| human immunodeficiency virus infectious disease

| class of disease

| viral infectious disease
Lentivirus infectious disease

| disease affecting the human immune system

| [http://www.disease-ontology.org/?id=DOID:526 DOID:526]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.673.480 C20.673.480]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.778.640.400 C01.778.640.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.782.815.616.400 C01.925.782.815.616.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.813.400 C01.925.813.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.221.250.875 C01.221.250.875]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.221.812.640.400 C01.221.812.640.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.100.937.640.400 C12.100.937.640.400]

|

|

|-

| human monocytic ehrlichiosis

| class of disease

| ehrlichiosis
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050026 DOID:0050026]

|

|

| File:Echaff.jpg

|-

| humeroradial synostosis

| class of disease

| synostosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060467 DOID:0060467]

|

|

|

|-

| hyaline body myopathy

| class of disease

| congenital myopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111267 DOID:0111267]

|

|

|

|-

| hyaline fibromatosis syndrome

| class of disease

| autosomal recessive disease
connective tissue disease
fibromatosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111669 DOID:0111669]

|

|

|

|-

| hyalinizing trabecular adenoma

| class of disease

| follicular adenoma
thyroid adenoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:6203 DOID:6203]

|

|

|

|-

| hydranencephaly with renal aplasia-dysplasia

| class of disease

| genetic disease
autosomal recessive disease
syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080327 DOID:0080327]

|

|

|

|-

| hydrocele

| class of disease

| male reproductive system disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:9912 DOID:9912]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.882 C12.294.882]

| Hydrocele

| File:Gray1148.png

|-

| hydrolethalus syndrome 1

| class of disease

| hydrolethalus syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111355 DOID:0111355]

|

|

|

|-

| hydrolethalus syndrome 2

| class of disease

| hydrolethalus syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111356 DOID:0111356]

|

|

|

|-

| hydronephrosis

| class of disease

| urinary tract obstruction
kidney disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:11111 DOID:11111]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.419.307 C12.777.419.307]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.419.307 C13.351.968.419.307]

| Hydronephrosis

|

|-

| hydrophthalmos

| class of disease

| primary congenital glaucoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11212 DOID:11212]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.250.480 C11.250.480]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.525.381.407.480 C11.525.381.407.480]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.384.480 C16.131.384.480]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.614.438 C16.614.438]

|

|

|-

| hydrops of gallbladder

| class of disease

| gallbladder disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9717 DOID:9717]

|

|

|

|-

| hyper IgE recurrent infection syndrome 2

| class of disease

| autosomal recessive disease
Job's syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080594 DOID:0080594]

|

|

|

|-

| hyper IgE recurrent infection syndrome 3

| class of disease

| Job's syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080595 DOID:0080595]

|

|

|

|-

| hyper IgE recurrent infection syndrome 4

| class of disease

| autosomal recessive disease
Job's syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080596 DOID:0080596]

|

|

|

|-

| hyper-IgM syndrome type 4

| class of disease

| hyper IgM syndrome
hyperimmunoglobulin syndrome

| hyperimmunoglobulin syndrome characterized by normal or increased serum IgM concentrations associated with low or absent serum IgG, IgA, and IgE concentrations, indicating a defect in the class-switch recombination (CSR) process

| [http://www.disease-ontology.org/?id=DOID:0060760 DOID:0060760]

|

|

|

|-

| hyperalphalipoproteinemia 1

| class of disease

| cholesterol-ester transfer protein deficiency
autosomal dominant disease
hyperalphalipoproteinemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111369 DOID:0111369]

|

|

|

|-

| hyperandrogenism

| class of disease

| gonadal disease
sex differentiation disease
disease

| medical condition characterized by excessive levels of androgens in the body

| [http://www.disease-ontology.org/?id=DOID:11613 DOID:11613]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.875.253.064.500 C12.050.351.875.253.064.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.875.253.090.750 C12.050.351.875.253.090.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.316.064.500 C16.131.939.316.064.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.316.129.750 C16.131.939.316.129.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.119.064.500 C19.391.119.064.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.119.090.750 C19.391.119.090.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.706.316.064.500 C12.200.706.316.064.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.706.316.090.750 C12.200.706.316.090.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.800.316.064.500 C12.800.316.064.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.800.316.090.750 C12.800.316.090.750]

| Hyperandrogenism

|

|-

| hypercalcemia

| class of disease

| calcium metabolism disease
disease

| high calcium (Ca2+) level in the blood serum

| [http://www.disease-ontology.org/?id=DOID:12678 DOID:12678]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.174.451 C18.452.174.451]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.950.340 C18.452.950.340]

| Hypercalcemia

|

|-

| hypercalcemic sarcoidosis

| class of disease

| sarcoidosis
hypercalcemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13407 DOID:13407]

|

|

|

|-

| hypercalcemic type ovarian small cell carcinoma

| class of disease

| ovarian small cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7651 DOID:7651]

|

|

|

|-

| hypercementosis

| class of disease

| teeth hard tissue disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12733 DOID:12733]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.793.422 C07.793.422]

|

|

|-

| hyperekplexia 1

| class of disease

| hyperekplexia
genetic disease
autosomal recessive disease
autosomal dominant disease

| hyperekplexia that has material basis in heterozygous, homozygous, or compound heterozygous mutation in the GLRA1 gene on chromosome 5q32

| [http://www.disease-ontology.org/?id=DOID:0060696 DOID:0060696]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.590 C10.228.590]

|

|

|-

| hyperekplexia 4

| class of disease

| hyperekplexia
autosomal recessive disease

| hyperekplexia that is characterized by extreme hypertonia, stiff and rigid appeareance and that has material basis in homozygous mutation in the ATAD1 gene on chromosome 10q23

| [http://www.disease-ontology.org/?id=DOID:0080581 DOID:0080581]

|

|

|

|-

| hyperglobulinemic purpura

| class of disease

| purpura

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3325 DOID:3325]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.454.550 C14.907.454.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.100.802.250 C15.378.100.802.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463.515.550 C15.378.463.515.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.414.950.250 C23.550.414.950.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.885.687.250 C23.888.885.687.250]

|

|

|-

| hyperglycemia

| class of disease
abnormally high value

| glucose metabolism disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:4195 DOID:4195]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.394.952 C18.452.394.952]

| Hyperglycemia

| File:Hyperglycemia.png

|-

| hyperhomocysteinemia

| class of disease

| sulfuraminoacidemia
amino acid metabolic disorder
disease

| amino acid metabolic disorder that involves an abnormally large level of homocysteine in the blood

| [http://www.disease-ontology.org/?id=DOID:9279 DOID:9279]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.100.480 C16.320.565.100.480]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.603.378 C18.452.603.378]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.100.480 C18.452.648.100.480]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.654.521.500.133.699.418 C18.654.521.500.133.699.418]

|

| File:L-Homocysteine.svg

|-

| hyperimmunoglobulin syndrome

| class of disease

| B cell deficiency

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2959 DOID:2959]

|

|

|

|-

| hyperinsulinemia

| class of disease

| endocrine pancreas disease
glucose metabolism disease
pancreas disease

| condition in which there are excess levels of insulin circulating in the blood relative to the level of glucose

| [http://www.disease-ontology.org/?id=DOID:2018 DOID:2018]

|

|

|

|-

| hyperlipoproteinemia type IV

| class of disease

| hyperlipidemia
familial hyperlipidemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:1172 DOID:1172]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.398.487 C16.320.565.398.487]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.500.500.644.490 C18.452.584.500.500.644.490]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.500.500.851.500 C18.452.584.500.500.851.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.398.487 C18.452.648.398.487]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.563.487 C18.452.584.563.487]

|

|

|-

| hypermanganesemia with dystonia

| class of disease

| metal metabolism disorder

| metal metabolism disorder that is characterized by involuntary, sustained muscle contractions (dystonia) and other uncontrolled movements resulting from excessive accumulation of manganese

| [http://www.disease-ontology.org/?id=DOID:0080535 DOID:0080535]

|

|

|

|-

| hypermanganesemia with dystonia 1

| class of disease

| hypermanganesemia with dystonia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080536 DOID:0080536]

|

|

|

|-

| hypermethioninemia

| class of disease

| amino acid metabolic disorder

| An amino acid metabolic disorder that involves an excess of the amino acid methionine, in the blood. This condition can occur when methionine is not broken down properly in the body.

| [http://www.disease-ontology.org/?id=DOID:0050544 DOID:0050544]

|

|

|

|-

| hypermobility of coccyx

| class of disease

| spondyloarthropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12537 DOID:12537]

|

|

|

|-

| hypermobility syndrome

| class of disease

| arthropathy
joint hypermobility
disease

| human disease: joints that stretch farther than normal

| [http://www.disease-ontology.org/?id=DOID:13781 DOID:13781]

|

| Hypermobility

| File:Doublejointedfinger.JPG

|-

| hyperopia

| class of disease
symptom or sign

| refractive error
disease

| visual defect which causes to see the far objects clearly and near objects unclearly

| [http://www.disease-ontology.org/?id=DOID:9834 DOID:9834]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.744.479 C11.744.479]

| Hyperopia

| File:Hypermetropia.svg

|-

| hyperostosis

| class of disease

| bone remodeling disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:205 DOID:205]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.540 C05.116.540]

| Hyperostosis

|

|-

| hyperphosphatemia

| class of disease

| phosphorus metabolism disease
genetic disease
disease

| electrolyte disorder in which there is an elevated level of phosphate in the blood.

| [http://www.disease-ontology.org/?id=DOID:0050459 DOID:0050459]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.750.199 C18.452.750.199]

| Hyperphosphatemia

|

|-

| hyperphosphatemic familial tumoral calcinosis

| class of disease

| calcinosis
genetic disease
Tumoral calcinosis
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111063 DOID:0111063]

|

|

|

|-

| hyperpigmentation of eyelid

| class of disease

| pigmentation disorder
eyelid disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10122 DOID:10122]

|

|

|

|-

| hyperpituitarism

| class of disease

| pituitary gland disease
anterior pituitary gland disease
disease

| endocrine disease

| [http://www.disease-ontology.org/?id=DOID:2444 DOID:2444]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.617.738.250 C10.228.140.617.738.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.700.355 C19.700.355]

|

|

|-

| hyperprolinemia type 1

| class of disease

| hyperprolinemia
autosomal recessive disease

| hyperprolinemia that has material basis in homozygous or compound heterozygous mutation in the proline dehydrogenase gene on chromosome 22q11

| [http://www.disease-ontology.org/?id=DOID:0080542 DOID:0080542]

|

|

|

|-

| hyperprolinemia type 2

| class of disease

| hyperprolinemia
autosomal recessive disease

| hyperprolinemia that has material basis in homozygous or compound heterozygous mutation in the pyrroline-5-carboxylate dehydrogenase gene on chromosome 1p36

| [http://www.disease-ontology.org/?id=DOID:0080543 DOID:0080543]

|

|

|

|-

| hyperprothrombinemia

| class of disease

| thrombophilia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080701 DOID:0080701]

|

|

|

|-

| hypersecretion glaucoma

| class of disease

| glaucoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11148 DOID:11148]

|

|

|

|-

| hypersensitivity vasculitis

| class of disease

| type III hypersensitivity

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9809 DOID:9809]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.940.910 C14.907.940.910]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.520.910 C20.543.520.910]

|

|

|-

| hypersomnia

| class of disease
symptom or sign

| sleep disorder
neurological disorder
sleep disturbance
disease

| excessive sleep

| [http://www.disease-ontology.org/?id=DOID:8619 DOID:8619]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.886.425.800.200 C10.886.425.800.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.870.400.800.200 F03.870.400.800.200]

|

|

|-

| hypersplenism

| class of disease

| splenic disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6376 DOID:6376]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.744.293 C15.604.744.293]

|

|

|-

| hypertensive encephalopathy

| class of disease

| intracranial hypertension
encephalomyelitis
disease

| general brain dysfunction due to significantly high blood pressure

| [http://www.disease-ontology.org/?id=DOID:9427 DOID:9427]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.631.500 C10.228.140.631.500]

|

|

|-

| hypertensive retinopathy

| class of disease

| retinal disease
complications of hypertension
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11561 DOID:11561]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.768.346 C11.768.346]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.489.815 C14.907.489.815]

| Hypertensive retinopathy

| File:Hypertensiveretinopathy.jpg

|-

| hyperthecosis

| class of disease

| ovarian disease

| hyperplasia of the theca interna of the ovary

| [http://www.disease-ontology.org/?id=DOID:7347 DOID:7347]

|

|

|

|-

| hypertrichosis

| class of disease

| hair diseases
epidermal disease
genetic hair anomaly
disease

| hair disease characterized by hair growth that is abnormal in quantity or location

| [http://www.disease-ontology.org/?id=DOID:420 DOID:420]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.329.875 C17.800.329.875]

| Hypertrichosis

| File:Alice Teennager.JPG

|-

| hypertrichosis of eyelid

| class of disease

| eyelid degenerative disease
hypertrichosis
nervous system heredodegenerative disease
eyelid disease

| hypertrichosis (disease) that involves the eyelid

| [http://www.disease-ontology.org/?id=DOID:11669 DOID:11669]

|

|

|

|-

| hypertrophic cardiomyopathy 1

| class of disease

| familial hypertrophic cardiomyopathy

| hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYH7 gene on chromosome 14q12

| [http://www.disease-ontology.org/?id=DOID:0110307 DOID:0110307]

|

|

|

|-

| hypertrophic cardiomyopathy 10

| class of disease

| familial hypertrophic cardiomyopathy

| hypertrophic cardiomyopathy that has material basis in mutation in the MYL2 gene

| [http://www.disease-ontology.org/?id=DOID:0110316 DOID:0110316]

|

|

|

|-

| hypertrophic cardiomyopathy 11

| class of disease

| familial hypertrophic cardiomyopathy

| hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the ACTC1 gene on chromosome 15q14

| [http://www.disease-ontology.org/?id=DOID:0110317 DOID:0110317]

|

|

|

|-

| hypertrophic cardiomyopathy 12

| class of disease

| familial hypertrophic cardiomyopathy

| hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the CSRP3 gene on chromosome 11p15

| [http://www.disease-ontology.org/?id=DOID:0110318 DOID:0110318]

|

|

|

|-

| hypertrophic cardiomyopathy 13

| class of disease

| familial hypertrophic cardiomyopathy

| hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TNNC1 gene on chromosome 3p21

| [http://www.disease-ontology.org/?id=DOID:0110319 DOID:0110319]

|

|

|

|-

| hypertrophic cardiomyopathy 14

| class of disease

| familial hypertrophic cardiomyopathy

| hypertrophic cardiomyopathy that has material basis in mutation in the MYH6 gene

| [http://www.disease-ontology.org/?id=DOID:0110320 DOID:0110320]

|

|

|

|-

| hypertrophic cardiomyopathy 15

| class of disease

| familial hypertrophic cardiomyopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110321 DOID:0110321]

|

|

|

|-

| hypertrophic cardiomyopathy 16

| class of disease

| familial hypertrophic cardiomyopathy

| hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYOZ2 gene on chromosome 4q26

| [http://www.disease-ontology.org/?id=DOID:0110322 DOID:0110322]

|

|

|

|-

| hypertrophic cardiomyopathy 17

| class of disease

| familial hypertrophic cardiomyopathy

| hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the junctophilin gene (JPH2) on chromosome 20q12

| [http://www.disease-ontology.org/?id=DOID:0110323 DOID:0110323]

|

|

|

|-

| hypertrophic cardiomyopathy 18

| class of disease

| familial hypertrophic cardiomyopathy

| A hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the gene encoding phospholamban (PLN) on chromosome 6q22.1.

| [http://www.disease-ontology.org/?id=DOID:0110324 DOID:0110324]

|

|

|

|-

| hypertrophic cardiomyopathy 2

| class of disease

| familial hypertrophic cardiomyopathy

| hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2)

| [http://www.disease-ontology.org/?id=DOID:0110308 DOID:0110308]

|

|

|

|-

| hypertrophic cardiomyopathy 20

| class of disease

| familial hypertrophic cardiomyopathy

| A hypertrophic cardiomyopathy that hhas material basis in heterozygous mutation in the NEXN gene on chromosome 1p31.1.

| [http://www.disease-ontology.org/?id=DOID:0110326 DOID:0110326]

|

|

|

|-

| hypertrophic cardiomyopathy 21

| class of disease

| familial hypertrophic cardiomyopathy

| A hypertrophic cardiomyopathy associated that has material basis in region 7p12.1-q21 variation.

| [http://www.disease-ontology.org/?id=DOID:0110311 DOID:0110311]

|

|

|

|-

| hypertrophic cardiomyopathy 25

| class of disease

| familial hypertrophic cardiomyopathy

| hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TCAP gene on chromosome 17q12

| [http://www.disease-ontology.org/?id=DOID:0110328 DOID:0110328]

|

|

|

|-

| hypertrophic cardiomyopathy 3

| class of disease

| familial hypertrophic cardiomyopathy

| hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22

| [http://www.disease-ontology.org/?id=DOID:0110309 DOID:0110309]

|

|

|

|-

| hypertrophic cardiomyopathy 4

| class of disease

| familial hypertrophic cardiomyopathy

| hypertrophic cardiomyopathy that has material basis in heterozygous, homozygous, or compound heterozygous mutation in the gene encoding cardiac myosin-binding protein C (MYBPC3) on chromosome 11p11

| [http://www.disease-ontology.org/?id=DOID:0110310 DOID:0110310]

|

|

|

|-

| hypertrophic cardiomyopathy 6

| class of disease

| familial hypertrophic cardiomyopathy

| hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the gene encoding the gamma-2 regulatory subunit of AMP-activated protein kinase (PRKAG2)

| [http://www.disease-ontology.org/?id=DOID:0110312 DOID:0110312]

|

|

|

|-

| hypertrophic cardiomyopathy 7

| class of disease

| familial hypertrophic cardiomyopathy

| A hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4.

| [http://www.disease-ontology.org/?id=DOID:0110313 DOID:0110313]

|

|

|

|-

| hypertrophic cardiomyopathy 8

| class of disease

| familial hypertrophic cardiomyopathy

| hypertrophic cardiomyopathy that has material basis in homozygous or heterozygous mutation in the MYL3 gene

| [http://www.disease-ontology.org/?id=DOID:0110314 DOID:0110314]

|

|

|

|-

| hypertrophic elongation of cervix

| class of disease

| cervix disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2251 DOID:2251]

|

|

|

|-

| hypertrophic pyloric stenosis

| class of disease

| pyloric stenosis

| pyloric stenosis characterized by the enlargement of the muscle surrounding the pylorus, causing severe projectile non-bilious vomiting

| [http://www.disease-ontology.org/?id=DOID:12638 DOID:12638]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.340.690.500 C06.405.748.340.690.500]

|

|

|-

| hypertrophy of tongue papillae

| class of disease

| tongue disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13333 DOID:13333]

|

|

|

|-

| hypertropia

| class of disease

| strabismus
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9837 DOID:9837]

|

| Hypertropia

|

|-

| hyperuricemia

| class of disease

| acquired metabolic disease
disease

| acquired metabolic disease that has material basis in an abnormally high level of uric acid in the blood.

| [http://www.disease-ontology.org/?id=DOID:1920 DOID:1920]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.449 C23.550.449]

| Hyperuricemia

|

|-

| hypervitaminosis A

| class of disease

| overnutrition
hypervitaminosis
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9972 DOID:9972]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.654.301 C18.654.301]

|

| File:All-trans-Retinol2.svg

|-

| hypervitaminosis D

| class of disease

| overnutrition
hypervitaminosis
disease

| excess of Vitamin D leading to abnormalities

| [http://www.disease-ontology.org/?id=DOID:9971 DOID:9971]

|

|

|

|-

| hypoactive sexual desire disorder

| class of disease

| psychosexual disorder
sexual dysfunction
disease

| sexual dysfunction

| [http://www.disease-ontology.org/?id=DOID:13868 DOID:13868]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.835 F03.835]

|

|

|-

| hypobetalipoproteinemia

| class of disease

| hypolipoproteinemia
disease

| hypolipoproteinemia characterized by permanently low levels of apolipoprotein B and LDL cholesterol resulting from an impaired ability to absorb and transport fats

| [http://www.disease-ontology.org/?id=DOID:1390 DOID:1390]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.398.500.440 C16.320.565.398.500.440]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.500.875.440 C18.452.584.500.875.440]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.398.500.440 C18.452.648.398.500.440]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.563.500.440 C18.452.584.563.500.440]

|

|

|-

| hypochondriasis

| class of disease

| somatoform disorder
nosophobia
disease

| somatoform disorder that involves an excessive preoccupation or worry about having a serious illness

| [http://www.disease-ontology.org/?id=DOID:12883 DOID:12883]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.875.450 F03.875.450]

|

|

|-

| hypochondrogenesis

| class of disease

| osteochondrodysplasia
achondrogenesis
genetic disease
spinal disease
monogenic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080044 DOID:0080044]

|

|

|

|-

| hypochromic anemia

| class of disease

| anemia

| generic term for any type of anemia in which the red blood cells (erythrocytes) are paler than normal

| [http://www.disease-ontology.org/?id=DOID:11759 DOID:11759]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.196 C15.378.071.196]

|

|

|-

| hypoglossal nerve disease

| class of disease

| glossopharyngeal nerve disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:13814 DOID:13814]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.525 C10.292.525]

|

|

|-

| hypoglossal nerve neoplasm

| class of disease

| cranial nerve neoplasm
hypoglossal nerve disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3198 DOID:3198]

|

|

|

|-

| hypoglycemic coma

| class of disease

| encephalopathy
coma
hypoglycemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:1607 DOID:1607]

|

|

|

|-

| hypogonadism

| class of disease

| gonadal disease
disease

| endocrine disease

| [http://www.disease-ontology.org/?id=DOID:1924 DOID:1924]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.482 C19.391.482]

| Hypogonadism

|

|-

| hypogonadotropic hypogonadism 12 with or without anosmia

| class of disease

| hypogonadotropic hypogonadism
genetic disease

| hypogonadotropic hypogonadism that has material basis in homozygous mutation in the GNRH1 gene on chromosome 8p21

| [http://www.disease-ontology.org/?id=DOID:0090072 DOID:0090072]

|

|

|

|-

| hypogonadotropic hypogonadism 16 with or without anosmia

| class of disease

| hypogonadotropic hypogonadism
genetic disease
autosomal dominant disease

| hypogonadotropic hypogonadism that has material basis in mutation in the SEMA3A gene on chromosome 7, sometimes in association with mutations in other genes

| [http://www.disease-ontology.org/?id=DOID:0090080 DOID:0090080]

|

|

|

|-

| hypogonadotropic hypogonadism 2 with or without anosmia

| class of disease

| hypogonadotropic hypogonadism
genetic disease

| hypogonadotropic hypogonadism that has material basis in heterozygous mutation in the FGFR1 gene on chromosome 8p11, sometimes in association with mutation in other genes

| [http://www.disease-ontology.org/?id=DOID:0090083 DOID:0090083]

|

|

|

|-

| hypohidrosis

| class of disease

| sweat gland disease
abnormal sudomotor regulation

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11155 DOID:11155]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.946.370 C17.800.946.370]

|

|

|-

| hypolipoproteinemia

| class of disease

| lipid metabolism disorder
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1387 DOID:1387]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.398.500 C16.320.565.398.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.500.875 C18.452.584.500.875]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.398.500 C18.452.648.398.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.563.500 C18.452.584.563.500]

|

|

|-

| hypomyelinating leukodystrophy

| class of disease

| leukodystrophy
Hereditary CNS demyelinating disease

| leukodystrophy characterized by T2 hyperintensity and T1 iso- or hyperintensity of affected white matter in the central nervous system

| [http://www.disease-ontology.org/?id=DOID:0060786 DOID:0060786]

|

|

|

|-

| hypomyelinating leukodystrophy 14

| class of disease

| hypomyelinating leukodystrophy
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080296 DOID:0080296]

|

|

|

|-

| hypomyelinating leukoencephalopathy

| class of disease

| spinocerebellar ataxia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050987 DOID:0050987]

|

|

|

|-

| hypoparathyroidism, familial isolated

| class of disease

| genetic hypoparathyroidism
hypoparathyroidism

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111387 DOID:0111387]

|

|

|

|-

| hypopharynx cancer

| class of disease

| carcinoma
pharyngeal cancer
neoplasm of hypopharynx

| pharynx cancer that is located in the hypopharynx

| [http://www.disease-ontology.org/?id=DOID:8533 DOID:8533]

|

| Hypopharyngeal cancer

| File:HypopharynxCa.jpg

|-

| hypophosphatemic nephrolithiasis/osteoporosis

| class of disease

| kidney disease
familial hypophosphatemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080655 DOID:0080655]

|

|

|

|-

| hypopigmentation of eyelid

| class of disease

| eyelid degenerative disease
pigmentation disorder
eyelid disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:11668 DOID:11668]

|

|

|

|-

| hypopyon

| class of disease
symptom or sign

| iridocyclitis
eye symptom
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10443 DOID:10443]

|

| Hypopyon

| File:Hypopyon.jpg

|-

| hypopyon ulcer

| class of disease

| hypopyon
corneal ulcer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10442 DOID:10442]

|

|

|

|-

| hypospadias

| class of disease

| non-syndromic urogenital tract malformation of male
penile disease
congenital disorder
disease

| condition in which the urethra does not open from the head of the penis

| [http://www.disease-ontology.org/?id=DOID:10892 DOID:10892]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.494.400 C12.294.494.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.706.516 C12.706.516]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.875.466 C13.351.875.466]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.516 C16.131.939.516]

| Hypospadias

| File:Hypospadias3.jpg

|-

| hypothalamic disease

| class of disease

| thalamic disease
encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:1931 DOID:1931]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.617 C10.228.140.617]

|

|

|-

| hypothalamic neoplasm

| class of disease

| diencephalic neoplasm
brain cancer
connective tissue neoplasm
hypothalamic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3644 DOID:3644]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.614.250.195.885.500 C04.588.614.250.195.885.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.211.885.500 C10.228.140.211.885.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.617.477 C10.228.140.617.477]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.551.240.250.700.500 C10.551.240.250.700.500]

|

|

|-

| hypothyroidism

| class of disease

| thyroid gland disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1459 DOID:1459]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.874.482 C19.874.482]

| Hypothyroidism

|

|-

| hypotonia-cystinuria syndrome

| class of disease

| syndrome
cystinuria
chromosomal deletion syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060858 DOID:0060858]

|

|

|

|-

| hypotrichosis 1

| class of disease

| hypotrichosis
genetic disease
autosomal dominant disease

| A hypotrichosis that has material basis in a autosomal dominant mutation of APCDD1 on chromosome 18p11.22.

| [http://www.disease-ontology.org/?id=DOID:0110698 DOID:0110698]

|

|

|

|-

| hypotrichosis 10

| class of disease

| hypotrichosis
genetic disease
autosomal recessive disease

| A hypotrichosis that has material basis in an autosomal recessive mutation on chromosome 7p22.3-p21.3.

| [http://www.disease-ontology.org/?id=DOID:0110707 DOID:0110707]

|

|

|

|-

| hypotrichosis 14

| class of disease

| hypotrichosis simplex
hypotrichosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080582 DOID:0080582]

|

|

|

|-

| hypotrichosis 4

| class of disease

| hypotrichosis
genetic disease
autosomal dominant disease

| A hypotrichosis that has material basis in a autosomal dominant mutation of HR on chromosome 8p21.3.

| [http://www.disease-ontology.org/?id=DOID:0110701 DOID:0110701]

|

|

|

|-

| hypotrichosis 5

| class of disease

| hypotrichosis
genetic disease
autosomal dominant disease

| A hypotrichosis that has material basis in a mutation on chromosome 1p21.1-q21.3.

| [http://www.disease-ontology.org/?id=DOID:0110702 DOID:0110702]

|

|

|

|-

| hypotrichosis 9

| class of disease

| hypotrichosis
genetic disease
autosomal recessive disease

| A hypotrichosis that has material basis in an autosomal recessive mutation on chromosome 10q11.23-q22.3.

| [http://www.disease-ontology.org/?id=DOID:0110706 DOID:0110706]

|

|

|

|-

| hypotrichosis of eyelid

| class of disease

| eyelid degenerative disease
hypotrichosis
eyelid disease

| hypotrichosis that involves the eyelid

| [http://www.disease-ontology.org/?id=DOID:11671 DOID:11671]

|

|

|

|-

| hypotropia

| class of disease

| strabismus

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9841 DOID:9841]

|

|

|

|-

| ichthyosis follicularis-alopecia-photophobia syndrome 1

| class of disease

| X-linked recessive disease
syndrome
Ichthyosis follicularis with alopecia and photophobia syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111821 DOID:0111821]

|

|

|

|-

| ideomotor apraxia

| class of disease

| apraxia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4627 DOID:4627]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.606.881.350.200 C10.597.606.881.350.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.604.882.350.200 C23.888.592.604.882.350.200]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F01.700.875.350.200 F01.700.875.350.200]

|

|

|-

| idiopathic corneal edema

| class of disease

| corneal edema

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11033 DOID:11033]

|

|

|

|-

| idiopathic generalized epilepsy 11

| class of disease

| generalized epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111312 DOID:0111312]

|

|

|

|-

| idiopathic generalized epilepsy 12

| class of disease

| generalized epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111313 DOID:0111313]

|

|

|

|-

| idiopathic generalized epilepsy 13

| class of disease

| generalized epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111314 DOID:0111314]

|

|

|

|-

| idiopathic generalized epilepsy 14

| class of disease

| generalized epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111315 DOID:0111315]

|

|

|

|-

| idiopathic generalized epilepsy 15

| class of disease

| generalized epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111316 DOID:0111316]

|

|

|

|-

| idiopathic generalized epilepsy 2

| class of disease

| generalized epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111317 DOID:0111317]

|

|

|

|-

| idiopathic generalized epilepsy 3

| class of disease

| generalized epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111318 DOID:0111318]

|

|

|

|-

| idiopathic generalized epilepsy 4

| class of disease

| generalized epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111319 DOID:0111319]

|

|

|

|-

| idiopathic generalized epilepsy 5

| class of disease

| generalized epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111320 DOID:0111320]

|

|

|

|-

| idiopathic generalized epilepsy 7

| class of disease

| generalized epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111321 DOID:0111321]

|

|

|

|-

| idiopathic generalized epilepsy 9

| class of disease

| generalized epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111323 DOID:0111323]

|

|

|

|-

| idiopathic orbital inflammatory disease

| class of disease

| orbital granuloma
chronic orbital inflammation

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9369 DOID:9369]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.675.679 C11.675.679]

|

| File:Inflammatory pseudotumor - Plasma cell granuloma Case 176 (5601449638).jpg

|-

| idiopathic peripheral autonomic neuropathy

| class of disease

| autonomic nervous system disease
autonomic peripheral neuropathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:11488 DOID:11488]

|

|

|

|-

| idiopathic progressive polyneuropathy

| class of disease

| polyneuropathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:10593 DOID:10593]

|

|

|

|-

| idiopathic pulmonary fibrosis

| class of disease

| idiopathic interstitial pneumonia
pulmonary fibrosis

| chronic, irreversible and ultimately fatal disease characterized by a progressive decline in lung function

| [http://www.disease-ontology.org/?id=DOID:0050156 DOID:0050156]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.483.487.500 C08.381.483.487.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.765.500 C08.381.765.500]

| Idiopathic pulmonary fibrosis

|

|-

| idiopathic scoliosis

| class of disease

| scoliosis

| scoliosis with no known cause

| [http://www.disease-ontology.org/?id=DOID:0060250 DOID:0060250]

|

|

|

|-

| ileal neoplasm

| class of disease

| small intestine neoplasm
ileal disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:10156 DOID:10156]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.476.411.501 C04.588.274.476.411.501]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.371.411.501 C06.301.371.411.501]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.249.411.501 C06.405.249.411.501]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.420.501 C06.405.469.420.501]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.491.501 C06.405.469.491.501]

|

|

|-

| ileitis

| class of disease

| Crohn's disease
enteritis

| inflammatory bowel disease characterized by inflammation located in ileum, has symptom diarrhea, has symptom abdominal pain, often in the right lower quadrant, has symptom weight loss

| [http://www.disease-ontology.org/?id=DOID:0060189 DOID:0060189]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.462.624 C06.405.205.462.624]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.326.875 C06.405.469.326.875]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.420.520 C06.405.469.420.520]

| Ileitis

|

|-

| ileum cancer

| class of disease

| small intestine cancer
ileal neoplasm

| small intestine cancer that is located in the ileum

| [http://www.disease-ontology.org/?id=DOID:10153 DOID:10153]

|

|

|

|-

| ileus

| class of disease

| bowel obstruction
disease

| human disease characterized by impairment of intestinal peristalsis; in modern language usually excludes mechanical bowel obstruction

| [http://www.disease-ontology.org/?id=DOID:8440 DOID:8440]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.531.492 C06.405.469.531.492]

| Ileus

|

|-

| iliac vein thrombophlebitis

| class of disease

| thrombophlebitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10880 DOID:10880]

|

|

|

|-

| immature cataract

| class of disease

| senile cataract

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10997 DOID:10997]

|

|

|

|-

| immature teratoma

| class of disease

| teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5563 DOID:5563]

|

|

|

|-

| immature teratoma of ovary

| class of disease

| malignant ovarian germ cell neoplasm
malignant non-dysgerminomatous germ cell tumor of ovary
ovarian biphasic or triphasic teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6331 DOID:6331]

|

|

|

|-

| immune disorder

| class of disease

| disease of anatomical entity

| a disease of the immune system

| [http://www.disease-ontology.org/?id=DOID:2914 DOID:2914]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20 C20]

| Diseases and disorders of the immune system

|

|-

| immune system cancer

| class of disease

| organ system cancer
immune disorder

| organ system cancer located in the immune system that is characterized by uncontrolled cellular proliferation in organs of the immune system

| [http://www.disease-ontology.org/?id=DOID:0060083 DOID:0060083]

|

|

|

|-

| immune system organ benign neoplasm

| class of disease

| organ system benign neoplasm
immune disorder

| organ system benign neoplasm located in the immune system organs

| [http://www.disease-ontology.org/?id=DOID:0060092 DOID:0060092]

|

|

|

|-

| immune-complex glomerulonephritis

| class of disease

| glomerulonephritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4784 DOID:4784]

|

|

|

|-

| immunodeficiency 11A

| class of disease

| autosomal recessive disease
severe combined immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111957 DOID:0111957]

|

|

|

|-

| immunodeficiency 11B

| class of disease

| autosomal dominant disease
T cell deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111958 DOID:0111958]

|

|

|

|-

| immunodeficiency 15A

| class of disease

| autosomal dominant disease
combined immunodeficiency
severe combined immunodeficiency due to IKK2 deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111960 DOID:0111960]

|

|

|

|-

| immunodeficiency 15B

| class of disease

| severe combined immunodeficiency
autosomal recessive disease
severe combined immunodeficiency due to IKK2 deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111959 DOID:0111959]

|

|

|

|-

| immunodeficiency 18

| class of disease

| autosomal recessive disease
primary immunodeficiency disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111971 DOID:0111971]

|

|

|

|-

| immunodeficiency 19

| class of disease

| autosomal recessive disease
severe combined immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111972 DOID:0111972]

|

|

|

|-

| immunodeficiency 28

| class of disease

| autosomal recessive disease
primary immunodeficiency disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111995 DOID:0111995]

|

|

|

|-

| immunodeficiency 32A

| class of disease

| autosomal dominant disease
dendritic cell deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111986 DOID:0111986]

|

|

|

|-

| immunodeficiency 32B

| class of disease

| monocyte, dendritic cell, and NK cell deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111985 DOID:0111985]

|

|

|

|-

| immunodeficiency 45

| class of disease

| autosomal recessive disease
primary immunodeficiency disease
primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111994 DOID:0111994]

|

|

|

|-

| immunodeficiency 51

| class of disease

| primary immunodeficiency disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111996 DOID:0111996]

|

|

|

|-

| immunodeficiency 52

| class of disease

| T cell deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111983 DOID:0111983]

|

|

|

|-

| immunodeficiency 53

| class of disease

| autosomal recessive disease
combined immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111992 DOID:0111992]

|

|

|

|-

| immunodeficiency 55

| class of disease

| autosomal recessive disease
combined immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111993 DOID:0111993]

|

|

|

|-

| immunodeficiency 57

| class of disease

| autosomal recessive disease
primary immunodeficiency disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111952 DOID:0111952]

|

|

|

|-

| immunodeficiency 58

| class of disease

| autosomal recessive disease
combined immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111984 DOID:0111984]

|

|

|

|-

| immunodeficiency 59

| class of disease

| autosomal recessive disease
B cell and dendritic cell deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111974 DOID:0111974]

|

|

|

|-

| immunodeficiency 60

| class of disease

| combined immunodeficiency
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111954 DOID:0111954]

|

|

|

|-

| immunodeficiency 62

| class of disease

| autosomal recessive disease
B cell deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111991 DOID:0111991]

|

|

|

|-

| immunodeficiency 63

| class of disease

| autosomal recessive disease
T cell and NK cell immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111997 DOID:0111997]

|

|

|

|-

| immunodeficiency 64

| class of disease

| T cell, B cell, and NK cell deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111980 DOID:0111980]

|

|

|

|-

| immunodeficiency 65

| class of disease

| primary immunodeficiency disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111978 DOID:0111978]

|

|

|

|-

| immunodeficiency 66

| class of disease

| primary immunodeficiency disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111998 DOID:0111998]

|

|

|

|-

| immunodeficiency 69

| class of disease

| autosomal recessive disease
T cell and NK cell immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112006 DOID:0112006]

|

|

|

|-

| immunodeficiency 70

| class of disease

| autosomal dominant disease
combined immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112005 DOID:0112005]

|

|

|

|-

| immunodeficiency 71

| class of disease

| combined immunodeficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112004 DOID:0112004]

|

|

|

|-

| immunodeficiency 72

| class of disease

| autosomal recessive disease
combined immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112015 DOID:0112015]

|

|

|

|-

| immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia

| class of disease

| autosomal dominant disease
combined immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112061 DOID:0112061]

|

|

|

|-

| immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia

| class of disease

| combined immunodeficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112062 DOID:0112062]

|

|

|

|-

| immunodeficiency-centromeric instability-facial anomalies syndrome

| class of disease

| autosomal recessive disease
DNA repair defect other than combined T-cell and B-cell immunodeficiencies
syndrome

| autosomal recessive disease characterized by immunodeficiency, rearrangements in the vicinity of the centromeres of chromosomes 1, 9, and 16 and facial anomalies in most cases

| [http://www.disease-ontology.org/?id=DOID:0090007 DOID:0090007]

|

|

|

|-

| immunoglobulin A deficiency

| class of disease

| selective immunoglobulin deficiency disease
B cell deficiency
genetic disease
disease

| dysgammaglobulinemia characterized by a deficiency of immunoglobulin A

| [http://www.disease-ontology.org/?id=DOID:0060025 DOID:0060025]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.147.333.500 C15.378.147.333.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.673.430.500 C20.673.430.500]

|

|

|-

| immunoglobulin beta deficiency

| class of disease

| B cell deficiency

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060026 DOID:0060026]

|

|

|

|-

| imperforate anus

| class of disease

| congenital disorder
atresia
anorectal anomalies
anal disease

| congenital disorder of digestive system

| [http://www.disease-ontology.org/?id=DOID:10488 DOID:10488]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.198.050 C06.198.050]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.314.094 C16.131.314.094]

| Imperforate anus

| File:Rectovestibular fistula in females.jpg

|-

| impulse control disorder

| class of disease

| mental disorder
disease

| disease of mental health that involves a failure to resist an impulsive act or behaviour that may be harmful to self or others

| [http://www.disease-ontology.org/?id=DOID:10937 DOID:10937]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.250 F03.250]

| Habit and impulse disorders

|

|-

| in situ carcinoma

| class of disease

| pre-malignant neoplasm
In situ neoplasm
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:8719 DOID:8719]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.240 C04.557.470.200.240]

| Carcinomas in situ

| File:In situ carcinoma-en.svg

|-

| inborn errors of purine–pyrimidine metabolism

| class of disease

| inherited metabolic disorder

| inherited metabolic disorder involving dysfunction of purine and pyrimidine metabolism

| [http://www.disease-ontology.org/?id=DOID:653 DOID:653]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.798 C16.320.565.798]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.798 C18.452.648.798]

|

|

|-

| inborn errors pyruvate metabolism

| class of disease

| carbohydrate metabolic disorder

| human disease

| [http://www.disease-ontology.org/?id=DOID:3648 DOID:3648]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.202.810 C16.320.565.202.810]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.202.810 C18.452.648.202.810]

|

|

|-

| inborn metabolic brain disease

| class of disease

| metabolic brain disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:889 DOID:889]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.163.100 C10.228.140.163.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.189 C16.320.565.189]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.132.100 C18.452.132.100]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.189 C18.452.648.189]

|

|

|-

| inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1

| class of disease

| inclusion body myopathy with Paget disease of bone and frontotemporal dementia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111385 DOID:0111385]

|

|

|

|-

| inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2

| class of disease

| inclusion body myopathy with Paget disease of bone and frontotemporal dementia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111384 DOID:0111384]

|

|

|

|-

| inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3

| class of disease

| inclusion body myopathy with Paget disease of bone and frontotemporal dementia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111386 DOID:0111386]

|

|

|

|-

| incontinentia pigmenti achromians

| class of disease

| skin disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3156 DOID:3156]

|

|

|

|-

| indeterminate leprosy

| class of disease

| leprosy
paucibacillary leprosy

| leprosy that is an early form of the disease which causes one to a few hypopigmented or erythematous macules

| [http://www.disease-ontology.org/?id=DOID:11851 DOID:11851]

|

|

|

|-

| indolent myeloma

| class of disease

| smouldering myeloma
multiple myeloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9550 DOID:9550]

|

|

|

|-

| indolent systemic mastocytosis

| class of disease

| mastocytoma
systemic mastocytosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:4660 DOID:4660]

|

|

|

|-

| infancy electroclinical syndrome

| class of disease

| electroclinical syndrome
epilepsy syndrome
Epilepsy in children

| electroclinical syndrome with onset in infancy occurring between birth and one year of age

| [http://www.disease-ontology.org/?id=DOID:0050703 DOID:0050703]

|

|

|

|-

| infant gynecomastia

| class of disease

| breast disease
gynecomastia

| human disease

| [http://www.disease-ontology.org/?id=DOID:11603 DOID:11603]

|

|

|

|-

| infantile epileptic encephalopathy

| class of disease

| infancy electroclinical syndrome
childhood onset epileptic encephalopathy
West syndrome

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2481 DOID:2481]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490.375.760 C10.228.140.490.375.760]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490.493.875 C10.228.140.490.493.875]

|

|

|-

| infantile hypophosphatasia

| class of disease

| hypophosphatasia

| A hypophosphatasia that has material basis in an autosomal recessive mutation of ALPL on chromosome 1p36.12.

| [http://www.disease-ontology.org/?id=DOID:0110914 DOID:0110914]

|

|

|

|-

| infantile or early childhood epileptic encephalopathy 1

| class of disease

| electroclinical syndrome
infantile epileptic encephalopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080472 DOID:0080472]

|

|

|

|-

| infantile or early childhood epileptic encephalopathy 2

| class of disease

| electroclinical syndrome
autosomal dominant disease

| electroclinical syndrome characterized by onset of seizures in infancy or early childhood, global developmental delay and variable intellectual disability that has material basis in heterozygous mutation in the GABRB2 gene on chromosome 5q34

| [http://www.disease-ontology.org/?id=DOID:0080471 DOID:0080471]

|

|

|

|-

| infantile osteopetrosis with neuroaxonal dysplasia

| class of disease

| neuroaxonal dystrophy
osteopetrosis

| This syndrome is characterized by osteopetrosis, agenesis of the corpus callosum, cerebral atrophy and a small hippocampus

| [http://www.disease-ontology.org/?id=DOID:0070343 DOID:0070343]

|

|

|

|-

| infantile-onset distal myopathy

| class of disease

| distal muscular dystrophy

| distal muscular dystrophy characterized by autosomal dominant inheritance, infantile onset and progressive disease development

| [http://www.disease-ontology.org/?id=DOID:0070196 DOID:0070196]

|

|

|

|-

| infected hydrocele

| class of disease

| hydrocele

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9911 DOID:9911]

|

|

|

|-

| infectious disease

| class of disease

| disease
infection associated with diseases

| disease caused by infection of pathogenic biological agents in a host organism

| [http://www.disease-ontology.org/?id=DOID:0050117 DOID:0050117]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.539.221 C01.539.221]

| Infectious diseases and disorders

| File:Malaria.jpg

|-

| infective endocarditis

| class of disease

| endocarditis
cardiovascular Infection
infectious disease
disease

| endocarditis that is characterized by inflammation of the endocardium caused by infectious agents.

| [http://www.disease-ontology.org/?id=DOID:0060000 DOID:0060000]

|

|

| File:Haemophilus parainfluenzae Endocarditis PHIL 851 lores.jpg

|-

| infective urethral stricture

| class of disease

| urethral stricture

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13658 DOID:13658]

|

|

|

|-

| inferior myocardial infarction

| class of disease

| myocardial infarction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5850 DOID:5850]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.647.500.187 C14.280.647.500.187]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.585.500.187 C14.907.585.500.187]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.513.355.750.187 C23.550.513.355.750.187]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.717.489.750.187 C23.550.717.489.750.187]

|

|

|-

| inferolateral myocardial infarct

| class of disease

| myocardial infarction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5852 DOID:5852]

|

|

|

|-

| infertility

| class of disease
symptom or sign

| reproductive system disease
reproductive system symptom
disease

| inability of a person, animal or plant to reproduce by natural means that is no intervention of contraceptive techniques

| [http://www.disease-ontology.org/?id=DOID:5223 DOID:5223]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.365 C12.294.365]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.365 C13.351.500.365]

| Infertility

| File:Infertility causes.png

|-

| infertility due to extratesticular cause

| class of disease

| male infertility

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14096 DOID:14096]

|

|

|

|-

| infiltrating angiolipoma

| class of disease

| angiolipoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3615 DOID:3615]

|

|

|

|-

| infiltrating bladder lymphoepithelioma-like carcinoma

| class of disease

| invasive bladder transitional cell carcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:7600 DOID:7600]

|

|

|

|-

| infiltrating bladder urothelial carcinoma sarcomatoid variant

| class of disease

| invasive bladder transitional cell carcinoma
sarcomatoid transitional cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7553 DOID:7553]

|

|

|

|-

| infiltrating lipoma

| class of disease

| lipoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7014 DOID:7014]

|

|

|

|-

| infiltrating nipple syringomatous adenoma

| class of disease

| nipple neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7839 DOID:7839]

|

|

|

|-

| infiltrating renal pelvis transitional cell carcinoma

| class of disease

| renal pelvis transitional cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050620 DOID:0050620]

|

|

|

|-

| infiltrating ureter transitional cell carcinoma

| class of disease

| ureter transitional cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6845 DOID:6845]

|

|

|

|-

| infiltrative basal cell carcinoma

| class of disease

| basal-cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4299 DOID:4299]

|

|

|

|-

| inflamed seborrheic keratosis

| class of disease

| seborrheic keratosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11685 DOID:11685]

|

|

|

|-

| inflammatory MFH

| class of disease

| malignant fibrous histiocytoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6192 DOID:6192]

|

|

|

|-

| inflammatory and toxic neuropathy

| class of disease

| peripheral neuropathy
acquired peripheral neuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2537 DOID:2537]

|

|

|

|-

| inflammatory bowel disease 1

| class of disease

| inflammatory bowel diseases
genetic disease

| An inflammatory bowel disease that has material basis in mutations in the NOD2 gene on chromosome 16q12.1.

| [http://www.disease-ontology.org/?id=DOID:0110892 DOID:0110892]

|

|

|

|-

| inflammatory bowel disease 11

| class of disease

| inflammatory bowel diseases
genetic disease

| inflammatory bowel disease that has material basis in variation in the chromosome region 7q22

| [http://www.disease-ontology.org/?id=DOID:0110894 DOID:0110894]

|

|

|

|-

| inflammatory bowel disease 12

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| An inflammatory bowel disease that has material basis in variation in the chromosome region 3p21.3

| [http://www.disease-ontology.org/?id=DOID:0110887 DOID:0110887]

|

|

|

|-

| inflammatory bowel disease 13

| class of disease

| inflammatory bowel diseases
genetic disease

| An inflammatory bowel disease that has material basis in variation in the ABCB1 gene on chromosome 7q21.1.

| [http://www.disease-ontology.org/?id=DOID:0110893 DOID:0110893]

|

|

|

|-

| inflammatory bowel disease 15

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| inflammatory bowel disease that has material basis in variation in the chromosome region 10q21

| [http://www.disease-ontology.org/?id=DOID:0110897 DOID:0110897]

|

|

|

|-

| inflammatory bowel disease 16

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| inflammatory bowel disease that has material basis in variation in the chromosome region 9q32

| [http://www.disease-ontology.org/?id=DOID:0110896 DOID:0110896]

|

|

|

|-

| inflammatory bowel disease 17

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| An inflammatory bowel disease that has material basis in variation in the IL23R gene on chromosome 1p31.3.

| [http://www.disease-ontology.org/?id=DOID:0110883 DOID:0110883]

|

|

|

|-

| inflammatory bowel disease 18

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| An inflammatory bowel disease that has material basis in variation in the chromosome region 5p13.1.

| [http://www.disease-ontology.org/?id=DOID:0110888 DOID:0110888]

|

|

|

|-

| inflammatory bowel disease 2

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| An inflammatory bowel disease that has material basis in variation in the chromosome region 12p13.2-q24.1.

| [http://www.disease-ontology.org/?id=DOID:0110900 DOID:0110900]

|

|

|

|-

| inflammatory bowel disease 20

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| inflammatory bowel disease that has material basis in variation in the chromosome region 10q23-q24

| [http://www.disease-ontology.org/?id=DOID:0110898 DOID:0110898]

|

|

|

|-

| inflammatory bowel disease 21

| class of disease

| inflammatory bowel diseases
genetic disease
autosomal dominant disease

| inflammatory bowel disease that has material basis in variation in the chromosome region 18p11

| [http://www.disease-ontology.org/?id=DOID:0110906 DOID:0110906]

|

|

|

|-

| inflammatory bowel disease 22

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| An inflammatory bowel disease that has material basis in variation in the chromosome region 17q21.2.

| [http://www.disease-ontology.org/?id=DOID:0110905 DOID:0110905]

|

|

|

|-

| inflammatory bowel disease 23

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| An inflammatory bowel disease that has material basis in variation in the chromosome region 1q32.1.

| [http://www.disease-ontology.org/?id=DOID:0110884 DOID:0110884]

|

|

|

|-

| inflammatory bowel disease 24

| class of disease

| inflammatory bowel diseases
genetic disease

| inflammatory bowel disease that has material basis in variation in the chromosome 20q13

| [http://www.disease-ontology.org/?id=DOID:0110908 DOID:0110908]

|

|

|

|-

| inflammatory bowel disease 26

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| inflammatory bowel disease that has material basis in variation in the chromosome region 12q15

| [http://www.disease-ontology.org/?id=DOID:0110901 DOID:0110901]

|

|

|

|-

| inflammatory bowel disease 27

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| An inflammatory bowel disease that has material basis in variation in the chromosome region 13q13.3

| [http://www.disease-ontology.org/?id=DOID:0110902 DOID:0110902]

|

|

|

|-

| inflammatory bowel disease 3

| class of disease

| inflammatory bowel diseases
genetic disease
autosomal dominant disease

| An inflammatory bowel disease that has material basis in variation in the chromosome region 6p21.3.

| [http://www.disease-ontology.org/?id=DOID:0110891 DOID:0110891]

|

|

|

|-

| inflammatory bowel disease 4

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| inflammatory bowel disease that has material basis in variation in the chromosome region 14q11-q12

| [http://www.disease-ontology.org/?id=DOID:0110903 DOID:0110903]

|

|

|

|-

| inflammatory bowel disease 5

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| inflammatory bowel disease that has material basis in variation in the chromosome region 5q31

| [http://www.disease-ontology.org/?id=DOID:0110889 DOID:0110889]

|

|

|

|-

| inflammatory bowel disease 6

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| inflammatory bowel disease that has material basis in variation in the chromosome region 19p13

| [http://www.disease-ontology.org/?id=DOID:0110907 DOID:0110907]

|

|

|

|-

| inflammatory bowel disease 7

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| inflammatory bowel disease that has material basis in variation in the chromosome region 1p36

| [http://www.disease-ontology.org/?id=DOID:0110882 DOID:0110882]

|

|

|

|-

| inflammatory bowel disease 8

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| inflammatory bowel disease that has material basis in variation in the chromosome region 16p

| [http://www.disease-ontology.org/?id=DOID:0110904 DOID:0110904]

|

|

|

|-

| inflammatory bowel disease 9

| class of disease

| inflammatory bowel diseases
genetic disease
monogenic disease

| inflammatory bowel disease that has material basis in variation in the chromosome region 3p26

| [http://www.disease-ontology.org/?id=DOID:0110886 DOID:0110886]

|

|

|

|-

| inflammatory bowel diseases

| class of disease

| intestinal disease
immune disorder
disease

| intestinal disease characterized by inflammation located in all parts of digestive tract

| [http://www.disease-ontology.org/?id=DOID:0050589 DOID:0050589]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.731 C06.405.205.731]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.432 C06.405.469.432]

| Inflammatory bowel diseases

| File:Cryptitis high mag.jpg

|-

| inflammatory breast carcinoma

| class of disease

| breast adenocarcinoma
invasive breast carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6263 DOID:6263]

|

|

|

|-

| inflammatory diarrhea

| class of disease

| diarrhea
mucositis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050132 DOID:0050132]

|

|

|

|-

| inflammatory leiomyosarcoma

| class of disease

| leiomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5251 DOID:5251]

|

|

|

|-

| inflammatory liposarcoma

| class of disease

| atypical lipomatous tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8233 DOID:8233]

|

|

|

|-

| inflammatory myofibroblastic tumour

| class of disease

| mesenchymal cell neoplasm
connective tissue benign neoplasm

| mesenchymal cell neoplasm that has material basis in myofibroblastic cells admixed with inflammatory cells

| [http://www.disease-ontology.org/?id=DOID:0050905 DOID:0050905]

|

| Inflammatory myofibroblastic tumour

|

|-

| inflammatory spondylopathy

| class of disease

| spondylitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12105 DOID:12105]

|

|

|

|-

| infratentorial cancer

| class of disease

| brain cancer
infratentorial neoplasm

| brain cancer that is located in the infratentorial region

| [http://www.disease-ontology.org/?id=DOID:4706 DOID:4706]

|

|

|

|-

| infundibulocystic basal cell carcinoma

| class of disease

| basal-cell carcinoma
inherited skin tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4279 DOID:4279]

|

|

|

|-

| inguinal hernia

| class of disease

| intestinal disease
disease

| intestinal disease characterized by a protrusion of abdominal cavity contests through the inguinal canal

| [http://www.disease-ontology.org/?id=DOID:0060320 DOID:0060320]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.300.707.374.875 C23.300.707.374.875]

| Inguinal hernia

| File:Inguinalhernia.gif

|-

| inherited metabolic disorder

| class of disease

| genetic disease
rare disease
metabolic disease
disease

| class of disease including endocrine diseases, nutritional diseases and metabolic diseases

| [http://www.disease-ontology.org/?id=DOID:655 DOID:655]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565 C16.320.565]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648 C18.452.648]

| Inborn errors of metabolism

|

|-

| inhibited female orgasm

| class of disease

| female reproductive system disease
anorgasmia
female orgasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7518 DOID:7518]
[http://www.disease-ontology.org/?id=DOID:11110 DOID:11110]

|

|

|

|-

| inner ear cancer

| class of disease

| auricular cancer
inner ear neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5102 DOID:5102]

|

|

|

|-

| inner ear disease

| class of disease

| ear disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:2952 DOID:2952]
[http://www.disease-ontology.org/?id=DOID:4539 DOID:4539]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.218.568 C09.218.568]

|

|

|-

| insulinoma

| class of disease

| pancreatic cystadenoma
benign neoplasms by histologic type
islet cell adenoma
disease

| tumor that produces too much insulin

| [http://www.disease-ontology.org/?id=DOID:3892 DOID:3892]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.035.100.852 C04.557.470.035.100.852]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.761.249.500 C04.588.274.761.249.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.475.249.500 C04.588.322.475.249.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.761.249.500 C06.301.761.249.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.689.667.249.500 C06.689.667.249.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.421.249.500 C19.344.421.249.500]

| Insulinoma

| File:Pancreatic insulinoma (2).JPG

|-

| integrative agnosia

| class of disease

| agnosia
apperceptive agnosia

| agnosia that is a loss of the ability to integrate these elements together into comprehensible perceptual wholes while recognizing elements of the whole

| [http://www.disease-ontology.org/?id=DOID:0060143 DOID:0060143]

|

|

|

|-

| integumentary system benign neoplasm

| class of disease

| organ system benign neoplasm
integumentary system neoplasm

| organ system benign neoplasm located in the integumentary system organs

| [http://www.disease-ontology.org/?id=DOID:0060121 DOID:0060121]

|

|

|

|-

| integumentary system cancer

| class of disease

| organ system cancer
integumentary system neoplasm
integumentary system disease

| organ system cancer that is located in the skin, hair and nails

| [http://www.disease-ontology.org/?id=DOID:0060122 DOID:0060122]

|

|

|

|-

| integumentary system disease

| class of disease

| disease of anatomical entity

| disease of anatomical entity that is located in the integumentary system comprising the skin and its appendages

| [http://www.disease-ontology.org/?id=DOID:16 DOID:16]

|

|

|

|-

| intellectual developmental disorder with short stature and behavioral abnormalities

| class of disease

| syndrome
autosomal recessive disease
syndromic intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111674 DOID:0111674]

|

|

|

|-

| intellectual disability

| class of disease

| specific developmental disorder
cognitive deficit
disability
disease

| generalized neurodevelopmental disorder

| [http://www.disease-ontology.org/?id=DOID:1059 DOID:1059]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.604.646 C23.888.592.604.646]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.606.360 C10.597.606.360]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F01.700.687 F01.700.687]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.625.539 F03.625.539]

| Intellectual disabilities

|

|-

| interdigitating dendritic cell sarcoma

| class of disease

| histiocytic and dendritic cell cancer
dendritic cell sarcoma

| histiocytic and dendritic cell cancer that effect dendritic cells

| [http://www.disease-ontology.org/?id=DOID:7848 DOID:7848]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.227.199 C04.557.227.199]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.250.390.199 C15.604.250.390.199]

|

|

|-

| interleukin-7 receptor alpha deficiency

| class of disease

| severe combined immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060015 DOID:0060015]

|

|

|

|-

| intermediate malignant teratoma

| class of disease

| immature teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7202 DOID:7202]

|

|

|

|-

| intermediate uveitis

| class of disease

| uveitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:12732 DOID:12732]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.879.900 C11.941.879.900]

| Intermediate uveitis

|

|-

| intermittent asthma

| class of disease

| chronic asthma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080812 DOID:0080812]

|

|

|

|-

| intermittent explosive disorder

| class of disease

| impulse control disorder
disease

| Mood disorder identified by frequent episodes of anger and rage

| [http://www.disease-ontology.org/?id=DOID:12401 DOID:12401]

|

|

|

|-

| intermittent proptosis

| class of disease

| orbital disease
exophthalmos

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12363 DOID:12363]

|

|

|

|-

| intermittent squint

| class of disease

| strabismus

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1942 DOID:1942]

|

|

|

|-

| intermixed schwannian stroma-rich ganglioneuroblastoma

| class of disease

| ganglioneuroblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5194 DOID:5194]

|

|

|

|-

| internal hemorrhoid

| class of disease

| hemorrhoid

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9749 DOID:9749]

|

|

|

|-

| internal resorption

| class of disease

| tooth resorption

| human disease

| [http://www.disease-ontology.org/?id=DOID:13239 DOID:13239]

|

|

|

|-

| internuclear ophthalmoplegia

| class of disease

| ophthalmoplegia
strabismus

| Human disease

| [http://www.disease-ontology.org/?id=DOID:538 DOID:538]

|

|

| File:Internuclear ophthalmoplegia.jpg

|-

| interstitial keratitis

| class of disease

| connective tissue disease
deep keratitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:9857 DOID:9857]

|

|

|

|-

| interstitial myocarditis

| class of disease

| mediastinitis
myocarditis

| Inflammation of the heart characterized by infiltration of the interstitial tissues by inflammatory cells, histiocytes, and the formation of granulomas. Giant cells are often present.

| [http://www.disease-ontology.org/?id=DOID:817 DOID:817]

|

|

|

|-

| interstitial nephritis

| class of disease

| nephritis
kidney disease
disease

| type of nephritis affecting the interstitium of the kidneys surrounding the tubules

| [http://www.disease-ontology.org/?id=DOID:1063 DOID:1063]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.777.419.570.643 C12.200.777.419.570.643]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.968.419.570.643 C12.050.351.968.419.570.643]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.950.419.570.643 C12.950.419.570.643]

| Tubulointerstitial disease

|

|-

| interval angle-closure glaucoma

| class of disease

| primary angle-closure glaucoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13549 DOID:13549]

|

|

|

|-

| intestinal atresia

| class of disease

| intestinal disease
intestinal malformation

| congenital disorder of digestive system

| [http://www.disease-ontology.org/?id=DOID:10486 DOID:10486]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.198.719 C06.198.719]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.445 C06.405.469.445]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.314.466 C16.131.314.466]

| Intestinal atresia

| File:DuodAtres.png

|-

| intestinal benign neoplasm

| class of disease

| gastrointestinal system benign neoplasm
intestinal neoplasm
intestinal disease

| gastrointestinal system benign neoplasm that is located in the intestine

| [http://www.disease-ontology.org/?id=DOID:4610 DOID:4610]

|

|

|

|-

| intestinal cancer

| class of disease

| gastrointestinal system cancer
intestinal neoplasm
intestinal disease

| gastrointestinal system cancer that is located in the intestine

| [http://www.disease-ontology.org/?id=DOID:10155 DOID:10155]

|

| Intestinal cancers

|

|-

| intestinal disaccharidase deficiency

| class of disease

| metabolic disease with intestinal involvement
intestinal disease
carbohydrate metabolic disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9868 DOID:9868]

|

|

|

|-

| intestinal disease

| class of disease

| gastrointestinal system disease

| gastrointestinal system disease that is located in the intestine

| [http://www.disease-ontology.org/?id=DOID:5295 DOID:5295]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469 C06.405.469]

| Diseases and disorders of intestines

|

|-

| intestinal impaction

| class of disease

| bowel obstruction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8448 DOID:8448]

|

|

|

|-

| intestinal neuroendocrine benign tumor

| class of disease

| intestinal benign neoplasm
gastrointestinal neuroendocrine benign tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4119 DOID:4119]

|

|

|

|-

| intestinal perforation

| class of disease

| intestinal disease
gastrointestinal perforation

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2074 DOID:2074]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.557 C06.405.469.557]

|

|

|-

| intestinal tuberculosis

| class of disease

| gastrointestinal tuberculosis
intestinal disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:13282 DOID:13282]

|

|

|

|-

| intestinal variant cervical mucinous adenocarcinoma

| class of disease

| cervical mucinous adenocarcinoma
intestinal type carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8339 DOID:8339]

|

|

|

|-

| intestinal volvulus

| class of disease

| bowel obstruction
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8445 DOID:8445]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.531.568 C06.405.469.531.568]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.300.970.500 C23.300.970.500]

| Volvulus

|

|-

| intestine carcinoma in situ

| class of disease

| carcinoma in situ of digestive organ
in situ carcinoma
intestinal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9024 DOID:9024]

|

|

|

|-

| intra-abdominal lymph node mast cell malignancy

| class of disease

| lymph node cancer
mast cell malignancy of lymph nodes
mastocytoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13005 DOID:13005]

|

|

|

|-

| intracerebral cystic meningioma

| class of disease

| cerebral meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6113 DOID:6113]

|

|

|

|-

| intracortical osteogenic sarcoma

| class of disease

| conventional central osteosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7602 DOID:7602]

|

|

|

|-

| intracranial abscess

| class of disease

| central nervous system disease
abscess

| central nervous system disease that is located in the skull and is characterized by a collection of pus (infected material) inside the skull

| [http://www.disease-ontology.org/?id=DOID:10095 DOID:10095]

|

|

|

|-

| intracranial aneurysm

| class of disease

| aneurysm
cerebrovascular disease
cerebral arterial disease
disease

| cerebrovascular disorder

| [http://www.disease-ontology.org/?id=DOID:10941 DOID:10941]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.510.600 C10.228.140.300.510.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.055.635 C14.907.055.635]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.560.300 C14.907.253.560.300]

| Cerebral aneurysms

| File:Aneurysem.jpg

|-

| intracranial arterial disease

| class of disease

| cerebrovascular disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:13089 DOID:13089]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.510 C10.228.140.300.510]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.560 C14.907.253.560]

|

|

|-

| intracranial arteriosclerosis

| class of disease

| arteriosclerosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:13097 DOID:13097]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.510.800 C10.228.140.300.510.800]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.137.126.372 C14.907.137.126.372]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.560.350 C14.907.253.560.350]

|

|

|-

| intracranial berry aneurysm

| class of disease

| intracranial aneurysm

| intracranial aneurysm with a characteristic rounded shape; the most common form of cerebral aneurysm

| [http://www.disease-ontology.org/?id=DOID:0060228 DOID:0060228]

|

|

|

|-

| intracranial berry aneurysm 11

| class of disease

| intracranial berry aneurysm

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080974 DOID:0080974]

|

|

|

|-

| intracranial berry aneurysm 9

| class of disease

| intracranial berry aneurysm

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080972 DOID:0080972]

|

|

|

|-

| intracranial cavernous angioma

| class of disease

| intracranial structure hemangioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2516 DOID:2516]

|

|

|

|-

| intracranial chondrosarcoma

| class of disease

| extraosseous chondrosarcoma
extraskeletal myxoid chondrosarcoma
intracranial tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7903 DOID:7903]

|

|

|

|-

| intracranial embolism

| class of disease

| cerebrovascular disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4372 DOID:4372]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.525.400 C10.228.140.300.525.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.566.300 C14.907.253.566.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.355.590.213.300 C14.907.355.590.213.300]

| Intracranial embolism

|

|-

| intracranial liposarcoma

| class of disease

| liposarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5714 DOID:5714]

|

|

|

|-

| intracranial primitive neuroectodermal tumor

| class of disease

| central nervous system primitive neuroectodermal neoplasm
medulloblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4788 DOID:4788]

|

|

|

|-

| intracranial structure hemangioma

| class of disease

| hemangioma
intracranial tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2517 DOID:2517]

|

|

|

|-

| intracranial thrombosis

| class of disease

| thrombosis
cerebrovascular disease
thromboembolism

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4193 DOID:4193]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.525.425 C10.228.140.300.525.425]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.566.350 C14.907.253.566.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.355.590.213.350 C14.907.355.590.213.350]

|

|

|-

| intracranial vasospasm

| class of disease

| vasospasm
cerebrovascular disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13100 DOID:13100]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.900 C10.228.140.300.900]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.951 C14.907.253.951]

|

|

|-

| intracystic papillary adenoma

| class of disease

| adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2682 DOID:2682]

|

|

|

|-

| intraductal breast myoepitheliosis

| class of disease

| breast myoepitheliosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8068 DOID:8068]

|

|

|

|-

| intraductal breast neoplasm

| class of disease

| breast benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3013 DOID:3013]

|

|

|

|-

| intraductal carcinoma

| class of disease

| breast carcinoma in situ
breast ductal carcinoma
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060074 DOID:0060074]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.275 C04.557.470.200.025.275]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.240.187.250 C04.557.470.200.240.187.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.615.275 C04.557.470.615.275]

| Ductal carcinoma in situ

| File:Breast DCIS histopathology (1).jpg

|-

| intraductal papillary breast neoplasm

| class of disease

| intraductal breast neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1628 DOID:1628]

|

|

|

|-

| intraductal papilloma

| class of disease

| breast benign neoplasm
papilloma
intraductal breast neoplasm
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1627 DOID:1627]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.615.670 C04.557.470.615.670]

| Intraductal papilloma

|

|-

| intrahepatic bile duct adenoma

| class of disease

| bile duct adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5437 DOID:5437]

|

|

|

|-

| intrahepatic bile duct cystadenoma

| class of disease

| bile duct cystadenoma
intrahepatic bile duct adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6733 DOID:6733]

|

|

|

|-

| intrahepatic biliary papillomatosis

| class of disease

| biliary papillomatosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8230 DOID:8230]

|

|

|

|-

| intrahepatic cholangiocarcinoma

| class of disease

| cholangiocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4928 DOID:4928]

|

|

|

|-

| intrahepatic cholestasis

| class of disease

| cholestasis

| medical condition

| [http://www.disease-ontology.org/?id=DOID:1852 DOID:1852]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.130.120.135.250 C06.130.120.135.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.150 C06.552.150]

|

|

|-

| intrahepatic cholestasis of pregnancy

| class of disease

| intrahepatic cholestasis
liver disease of pregnancy
disease

| intrahepatic cholestasis characterized by reversible cholestasis typically occurring in the second or third trimester of pregnancy, elevated serum aminotransferases and bile acid level and resolution of symptoms by 2 to 3 weeks after delivery

| [http://www.disease-ontology.org/?id=DOID:0070227 DOID:0070227]

|

|

| File:Cholestasis high mag.jpg

|-

| intrahepatic gall duct cancer

| class of disease

| gallbladder cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12298 DOID:12298]

|

|

|

|-

| intramuscular hemangioma

| class of disease

| hemangioma
muscle neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:468 DOID:468]

|

|

|

|-

| intraneural perineurioma

| class of disease

| perineurioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4696 DOID:4696]

|

|

|

|-

| intraocular lymphoma

| class of disease

| eye lymphoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:775 DOID:775]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386.435 C04.557.386.435]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.364.447 C04.588.364.447]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.569.417 C15.604.515.569.417]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.761.417 C20.683.515.761.417]

|

|

|-

| intraorbital meningioma

| class of disease

| orbital cancer
meningioma

| meningioma by site and orbital neoplasm that is located in the area around the eye sockets of the skull and results in pressure in the eyes, giving a bulging appearance

| [http://www.disease-ontology.org/?id=DOID:4141 DOID:4141]

|

|

|

|-

| intrapelvic lymph node leukemic reticuloendotheliosis

| class of disease

| lymph node cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12972 DOID:12972]

|

|

|

|-

| intratubular embryonal carcinoma

| class of disease

| embryonal testis carcinoma

| embryonal testis carcinoma that is located within a tubule

| [http://www.disease-ontology.org/?id=DOID:8275 DOID:8275]

|

|

|

|-

| intravascular angioleiomyoma

| class of disease

| angiomyoma
vascular neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4266 DOID:4266]

|

|

|

|-

| intravascular fasciitis

| class of disease

| pseudosarcomatous fibromatosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9603 DOID:9603]

|

|

|

|-

| intravenous leiomyomatosis

| class of disease

| leiomyomatosis
vascular disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5729 DOID:5729]

|

|

|

|-

| intraventricular meningioma

| class of disease

| cerebral ventricle cancer
meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3772 DOID:3772]

|

|

|

|-

| intrinsic asthma

| class of disease

| asthma
chronic asthma

| human disease

| [http://www.disease-ontology.org/?id=DOID:9360 DOID:9360]

|

|

|

|-

| intussusception

| class of disease

| bowel obstruction
genetic disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:8446 DOID:8446]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.531.577 C06.405.469.531.577]

| Intussusception

| File:VolvulusCT.PNG

|-

| invasive bladder transitional cell carcinoma

| class of disease

| bladder urothelial carcinoma
Invasive urothelial carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6477 DOID:6477]

|

|

|

|-

| invasive lobular carcinoma

| class of disease

| breast lobular carcinoma
invasive breast carcinoma
carcinoma
breast cancer
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3457 DOID:3457]

|

| Histopathology of invasive lobular carcinoma (ILC)

|

|-

| invasive malignant thymoma

| class of disease

| thymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3283 DOID:3283]

|

|

|

|-

| invasive tubular breast carcinoma

| class of disease

| breast adenocarcinoma
invasive ductal carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6587 DOID:6587]

|

|

|

|-

| inverted follicular keratosis

| class of disease

| seborrheic keratosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6945 DOID:6945]

|

| Inverted follicular keratosis

|

|-

| inverted papilloma

| class of disease

| papilloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3179 DOID:3179]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.700.600.610 C04.557.470.700.600.610]

| Inverted papillomas

|

|-

| inverted transitional papilloma

| class of disease

| transitional papilloma
inverted papilloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4630 DOID:4630]

|

|

|

|-

| iodine hypothyroidism

| class of disease

| hypothyroidism

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5083 DOID:5083]

|

|

|

|-

| iris cancer

| class of disease

| iris neoplasm
uveal cancer
iris disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3478 DOID:3478]

|

|

|

|-

| iris disease

| class of disease

| uveal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:240 DOID:240]
[http://www.disease-ontology.org/?id=DOID:4738 DOID:4738]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.375 C11.941.375]

|

|

|-

| iritis

| class of disease

| iris disease
anterior uveitis
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1406 DOID:1406]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.375.385 C11.941.375.385]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.879.780.880.448 C11.941.879.780.880.448]

|

|

|-

| iron deficiency anemia

| class of disease
symptom or sign

| deficiency anemia
nutritional deficiency disease
iron deficiency
hypochromic anemia
disease

| anemia caused by a lack of iron

| [http://www.disease-ontology.org/?id=DOID:11758 DOID:11758]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.196.300 C15.378.071.196.300]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.565.100 C18.452.565.100]

| Iron-deficiency anemia

| File:Heme b.svg

|-

| iron metabolism disease

| class of disease

| mineral metabolism disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2351 DOID:2351]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.565 C18.452.565]

|

|

|-

| irregular astigmatism

| class of disease

| astigmatism

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13919 DOID:13919]

|

|

|

|-

| irritable bowel syndrome

| class of disease
symptom or sign

| functional colonic disease
syndrome
intestinal disease
disease

| syndrome that is a functional bowel disorder characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause

| [http://www.disease-ontology.org/?id=DOID:9778 DOID:9778]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.158.272.608 C06.405.469.158.272.608]

| Irritable bowel syndrome

| File:Irritable bowel syndrome.jpg

|-

| irritant dermatitis

| class of disease

| contact dermatitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:2772 DOID:2772]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.174.255.400 C17.800.174.255.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.815.255.400 C17.800.815.255.400]

| Irritant contact dermatitis

|

|-

| ischemic bone disease

| class of disease

| bone disease
ischemia

| bone disease that results in an interruption of blood supply located in bone

| [http://www.disease-ontology.org/?id=DOID:0080008 DOID:0080008]

|

|

|

|-

| ischemic colitis

| class of disease

| colitis

| colitis caused by inadequate blood supply to the colon

| [http://www.disease-ontology.org/?id=DOID:0060181 DOID:0060181]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.265.115 C06.405.205.265.115]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.158.188.115 C06.405.469.158.188.115]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.286 C14.907.286]

| Ischemic colitis

|

|-

| ischemic fasciitis

| class of disease

| fasciitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:9601 DOID:9601]

|

| Ischemic fasciitis

|

|-

| ischemic neuropathy

| class of disease

| peripheral neuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1195 DOID:1195]

|

|

|

|-

| islet cell carcinoma

| class of disease

| islet cell tumor
gastrointestinal carcinoma
disease

| islet cell tumor that has material basis in epithelial cells

| [http://www.disease-ontology.org/?id=DOID:1798 DOID:1798]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.290 C04.557.470.200.025.290]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.761.500 C04.588.274.761.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.475.500 C04.588.322.475.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.761.500 C06.301.761.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.689.667.500 C06.689.667.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.421.500 C19.344.421.500]

| Pancreatic neuroendocrine tumors

|

|-

| islet cell tumor

| class of disease

| pancreatic cancer

| pancreatic cancer that is located in the pancreatic islet cells

| [http://www.disease-ontology.org/?id=DOID:1799 DOID:1799]

|

|

|

|-

| isocyanates allergic asthma

| class of disease

| allergic asthma
occupational asthma

| allergic asthma that has allergic trigger isocyanates

| [http://www.disease-ontology.org/?id=DOID:0040041 DOID:0040041]

|

|

|

|-

| isolated cryptophthalmia

| class of disease

| cryptophthalmos

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111717 DOID:0111717]

|

|

|

|-

| isolated ectopia lentis

| class of disease

| lens disease
ectopia lentis

| A lens disease characterized by abnormal stretching of the zonular fibers resulting in dislocation of the lens. This dislocation may be mild to severe and may progress with age.

| [http://www.disease-ontology.org/?id=DOID:0111148 DOID:0111148]

|

|

|

|-

| isolated growth hormone deficiency type IA

| class of disease

| isolated growth hormone deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060873 DOID:0060873]

|

|

|

|-

| isolated growth hormone deficiency type IB

| class of disease

| isolated growth hormone deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060874 DOID:0060874]

|

|

|

|-

| isolated growth hormone deficiency type II

| class of disease

| isolated growth hormone deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060872 DOID:0060872]

|

|

|

|-

| isolated growth hormone deficiency type III

| class of disease

| isolated growth hormone deficiency
X-linked recessive disease

| An isolated growth hormone deficiency characterized by dwarfism, variable occurence of hypogammaglobulinemia, and a generally good response to growth hormone therapy that has material basis in mutation in the BTK gene on chromosome Xq22.1.

| [http://www.disease-ontology.org/?id=DOID:0060875 DOID:0060875]

|

|

|

|-

| isolated microphthalmia

| class of disease

| microphthalmia

| microphthalmia that is not part of a larger syndrome

| [http://www.disease-ontology.org/?id=DOID:0080637 DOID:0080637]

|

|

|

|-

| isolated microphthalmia 1

| class of disease

| microphthalmia
genetic disease
isolated microphthalmia
autosomal recessive disease

| microphthalmia that has material basis in variation in the chromosomal region 14q32

| [http://www.disease-ontology.org/?id=DOID:0060840 DOID:0060840]

|

|

|

|-

| isoniazide allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger isoniazide

| [http://www.disease-ontology.org/?id=DOID:0040008 DOID:0040008]

|

|

|

|-

| isthmicoma

| class of disease

| hair follicle neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8426 DOID:8426]

|

| Isthmicoma

|

|-

| isthmus cancer

| class of disease

| uterine corpus cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9459 DOID:9459]

|

|

|

|-

| jaw cancer

| class of disease

| bone cancer
neoplasm of jaw

| bone cancer and jaw disease that is located in the jaw and results in a swollen jaw, results in numbness or a tingling sensation in jaw, and results in an abnormal growth of the jaw bone

| [http://www.disease-ontology.org/?id=DOID:1862 DOID:1862]

|

|

|

|-

| jaw-winking syndrome

| class of disease

| cranial nerve disease
ptosis
genetic peripheral neuropathy

| autosomal dominant condition with incomplete penetrance, in which nursing infants will have rhythmic upward jerking of their upper eyelid

| [http://www.disease-ontology.org/?id=DOID:560 DOID:560]

|

| Marcus Gunn phenomenon

|

|-

| jejunal adenocarcinoma

| class of disease

| jejunal cancer
adenocarcinoma

| jejunal cancer that is located in the jejunum and has material basis in epithelial tissue that has glandular origin

| [http://www.disease-ontology.org/?id=DOID:0050926 DOID:0050926]

|

|

|

|-

| jejunal cancer

| class of disease

| small intestine cancer
jejunal neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:13499 DOID:13499]

|

|

|

|-

| jejunal neoplasm

| class of disease

| small intestine neoplasm
jejunal disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3218 DOID:3218]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.476.411.523 C04.588.274.476.411.523]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.371.411.523 C06.301.371.411.523]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.249.411.523 C06.405.249.411.523]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.491.523 C06.405.469.491.523]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.600.523 C06.405.469.600.523]

|

|

|-

| jejunal somatostatinoma

| class of disease

| jejunal cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3216 DOID:3216]

|

|

|

|-

| junctional epidermolysis bullosa Herlitz type

| class of disease

| junctional epidermolysis bullosa
genetic disease
autosomal recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060737 DOID:0060737]

|

|

|

|-

| juvenile absence epilepsy

| class of disease

| adolescence-adult electroclinical syndrome

| adolescence-adult electroclinical syndrome statring between the age of ten to 17 years characterized by the occurrence of typical absence seizures

| [http://www.disease-ontology.org/?id=DOID:0060172 DOID:0060172]

|

|

|

|-

| juvenile absence epilepsy 1

| class of disease

| juvenile absence epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111324 DOID:0111324]

|

|

|

|-

| juvenile amyotrophic lateral sclerosis with dementia

| class of disease

| amyotrophic lateral sclerosis
juvenile amyotrophic lateral sclerosis

| juvenile amyotrophic lateral sclerosis that is slowly progressive with concomitantly progressive dementia

| [http://www.disease-ontology.org/?id=DOID:0110067 DOID:0110067]

|

|

|

|-

| juvenile ankylosing spondylitis

| class of disease

| autoimmune disease of musculoskeletal system
ankylosing spondylitis

| autoimmune disease of musculoskeletal system that is an ankylosing spondylitis with onset during childhood

| [http://www.disease-ontology.org/?id=DOID:0040092 DOID:0040092]

|

|

|

|-

| juvenile astrocytoma

| class of disease

| astrocytoma
childhood cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3079 DOID:3079]

|

|

|

|-

| juvenile dermatitis herpetiformis

| class of disease

| dermatitis herpetiformis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8507 DOID:8507]

|

|

|

|-

| juvenile glaucoma

| class of disease

| autosomal dominant disease
primary open angle glaucoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1068 DOID:1068]

|

|

|

|-

| juvenile myelomonocytic leukemia

| class of disease

| myelodysplastic/myeloproliferative neoplasm
monocytic leukemia
childhood leukemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050458 DOID:0050458]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.539.525 C04.557.337.539.525]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.190.615.520 C15.378.190.615.520]

|

|

|-

| juvenile myoclonic epilepsy

| class of disease

| adolescence-adult electroclinical syndrome
Idiopathic generalized epilepsy
myoclonic epilepsy

| adolescence-adult electroclinical syndrome that is characterized by brief, involuntary twitching of a muscle or a group of muscles (myoclonus) early in the morning with onset between 12 and 18 years

| [http://www.disease-ontology.org/?id=DOID:4890 DOID:4890]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490.493.063.670 C10.228.140.490.493.063.670]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490.375.130.670 C10.228.140.490.375.130.670]

|

|

|-

| juvenile myoclonic epilepsy 10

| class of disease

| juvenile myoclonic epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111325 DOID:0111325]

|

|

|

|-

| juvenile myoclonic epilepsy 3

| class of disease

| juvenile myoclonic epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111326 DOID:0111326]

|

|

|

|-

| juvenile myoclonic epilepsy 4

| class of disease

| juvenile myoclonic epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111327 DOID:0111327]

|

|

|

|-

| juvenile myoclonic epilepsy 9

| class of disease

| juvenile myoclonic epilepsy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111328 DOID:0111328]

|

|

|

|-

| juvenile pilocytic astrocytoma

| class of disease

| childhood pilocytic astrocytoma
pilocytic astrocytoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6811 DOID:6811]

|

|

|

|-

| juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome

| class of disease

| autosomal dominant disease
syndrome
juvenile polyposis syndrome
hereditary hemorrhagic telangiectasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111543 DOID:0111543]

|

|

|

|-

| juvenile type testicular granulosa cell tumor

| class of disease

| testicular granulosa cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6032 DOID:6032]

|

|

|

|-

| juvenile xanthogranuloma

| class of disease

| non-Langerhans-cell histiocytosis
histiocytosis
xanthogranuloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4424 DOID:4424]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.250.410.900 C15.604.250.410.900]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.973 C17.800.973]

| Juvenile xanthogranuloma

|

|-

| juvenile-onset Parkinson disease

| class of disease

| Parkinson's disease
young-onset Parkinson disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060893 DOID:0060893]

|

|

|

|-

| juxtacortical chondroma

| class of disease

| chondroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2601 DOID:2601]

|

|

|

|-

| juxtacortical chondrosarcoma

| class of disease

| chondrosarcoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:5866 DOID:5866]

|

|

|

|-

| juxtacortical osteosarcoma

| class of disease

| peripheral osteosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3373 DOID:3373]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.575.650.655 C04.557.450.565.575.650.655]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.620.655 C04.557.450.795.620.655]

|

|

|-

| keratinizing squamous cell carcinoma

| class of disease

| squamous cell carcinoma

| squamous cell carcinoma that presents as single, isolated cells with bizzare cytoplasmic shapes, intense cytoplasmic eosinophilia, and intensely hyperchromatic, angular nuclei in a background of necrotic and keratinous debris

| [http://www.disease-ontology.org/?id=DOID:5521 DOID:5521]

|

|

|

|-

| keratitis

| class of disease
symptom or sign

| corneal disease
eye inflammation
inflammatory disease
cornea symptom
disease

| corneal disease that is characterized by inflammation of the cornea.

| [http://www.disease-ontology.org/?id=DOID:4677 DOID:4677]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.204.564 C11.204.564]

| Keratitis

| File:Clare-314.jpg

|-

| keratoacanthoma

| class of disease

| cutaneous squamous-cell carcinoma
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3149 DOID:3149]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.417 C17.800.417]

| Keratoacanthoma

| File:Keratoacanthoma 2.jpg

|-

| keratoconjunctivitis

| class of disease

| keratitis
conjunctivitis
eye disease

| inflammation ("-itis") of the cornea and conjunctiva.

| [http://www.disease-ontology.org/?id=DOID:9368 DOID:9368]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.187.183.394 C11.187.183.394]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.204.564.585 C11.204.564.585]

| Keratoconjunctivitis

| File:Gade corneyo-djontivite clamidia3.jpg

|-

| keratoconjunctivitis sicca

| class of disease

| dry eye syndrome
keratoconjunctivitis
disease

| condition of having dry eyes

| [http://www.disease-ontology.org/?id=DOID:12895 DOID:12895]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.187.183.394.550 C11.187.183.394.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.204.564.585.630 C11.204.564.585.630]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.496.260.394 C11.496.260.394]

| Dry eye syndrome

|

|-

| keratomalacia

| class of disease

| corneal degeneration
vitamin A deficiency
keratitis related to vitamin deficiency
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11267 DOID:11267]

|

|

|

|-

| keratopathy

| class of disease

| corneal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2283 DOID:2283]

|

|

|

|-

| keratosis

| class of disease

| skin disease
keratoma
disease

| skin disease characterized by growth of keratin on the skin or mucous membranes

| [http://www.disease-ontology.org/?id=DOID:161 DOID:161]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.428 C17.800.428]

|

| File:Keratosis pilaris arm.jpg

|-

| keratosis follicularis spinulosa decalvans, autosomal dominant

| class of disease

| keratosis follicularis spinulosa decalvans

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080755 DOID:0080755]

|

|

|

|-

| keratosis pilaris atrophicans faciei

| class of disease

| keratosis pilaris atropicans

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080752 DOID:0080752]

|

|

|

|-

| keratosis pilaris atropicans

| class of disease

| keratosis pilaris
autosomal recessive disease
ichthyosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080751 DOID:0080751]

|

|

|

|-

| kernicterus

| class of disease
symptom or sign

| encephalopathy
neurometabolic disease
neonatal jaundice
disease

| congenital disorder of nervous system

| [http://www.disease-ontology.org/?id=DOID:2382 DOID:2382]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.163.480 C10.228.140.163.480]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.295.502 C15.378.295.502]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.614.304.502 C16.614.304.502]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.132.480 C18.452.132.480]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.306.502 C20.306.502]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.429.750 C23.550.429.750]

| Kernicterus

|

|-

| kernicterus due to isoimmunization

| class of disease

| neonatal jaundice
kernicterus

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12043 DOID:12043]

|

|

|

|-

| ketoprofen photoallergic dermatitis

| class of disease

| photodermatitis
drug allergy

| photoallergic dermatitis that has allergic trigger ketoprofen

| [http://www.disease-ontology.org/?id=DOID:0040060 DOID:0040060]

|

|

|

|-

| kidney angiomyolipoma

| class of disease

| kidney benign neoplasm
angiomyolipoma
benign perivascular tumor

| angiomyolipoma arising from the kidney

| [http://www.disease-ontology.org/?id=DOID:8411 DOID:8411]

|

| Renal angiomyolipoma

|

|-

| kidney benign neoplasm

| class of disease

| urinary system benign neoplasm
kidney neoplasm
kidney disease
lipoma

| A non-metastasizing neoplasm that arises from the kidney. Representative examples include cystic nephroma, metanephric adenoma, oncocytoma, and urothelial papilloma of the renal pelvis.

| [http://www.disease-ontology.org/?id=DOID:3116 DOID:3116]

|

|

|

|-

| kidney cancer

| class of disease

| urinary system cancer
kidney neoplasm
kidney disease
disease

| urinary system cancer that is located in the kidney

| [http://www.disease-ontology.org/?id=DOID:263 DOID:263]

|

| Cancers of kidney

|

|-

| kidney carcinoma in situ

| class of disease

| kidney disease
in situ carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9234 DOID:9234]

|

|

|

|-

| kidney clear cell sarcoma

| class of disease

| kidney cancer
kidney sarcoma
inherited renal tumor
clear-cell sarcoma

| kidney sarcoma that has material basis in clear cells that are characterized as cells that look clear when viewed under a microscope

| [http://www.disease-ontology.org/?id=DOID:4880 DOID:4880]

|

|

|

|-

| kidney cortex disease

| class of disease

| kidney disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080616 DOID:0080616]

|

|

|

|-

| kidney failure

| class of disease
symptom or sign

| kidney disease
impaired renal function disease
chronic renal disease
urological symptom
disease

| disease where the kidneys fail to adequately filter waste products from the blood

| [http://www.disease-ontology.org/?id=DOID:1074 DOID:1074]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.419.780 C12.777.419.780]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.419.780 C13.351.968.419.780]

|

|

|-

| kidney fibrosarcoma

| class of disease

| kidney sarcoma
fibrosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5982 DOID:5982]

|

|

|

|-

| kidney hemangiopericytoma

| class of disease

| kidney cancer

| kidney cancer which is manifested in the kidney

| [http://www.disease-ontology.org/?id=DOID:262 DOID:262]

|

|

|

|-

| kidney hypertrophy

| class of disease

| kidney disease

| Global enlargement of the renal parenchyma in one or both kidneys

| [http://www.disease-ontology.org/?id=DOID:9622 DOID:9622]

|

|

|

|-

| kidney infection

| class of disease

| infection
kidney disease
infectious disease

| type of infection that afflicts the kidneys

| [http://www.disease-ontology.org/?id=DOID:782 DOID:782]

|

|

|

|-

| kidney leiomyosarcoma

| class of disease

| kidney sarcoma

| leiomyosarcoma and sarcoma of kidney that is located in the kidney

| [http://www.disease-ontology.org/?id=DOID:5287 DOID:5287]

|

|

|

|-

| kidney lipoma

| class of disease

| kidney benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10194 DOID:10194]

|

|

|

|-

| kidney liposarcoma

| class of disease

| liposarcoma
kidney sarcoma
kidney cancer

| liposarcoma that is located in the kidney

| [http://www.disease-ontology.org/?id=DOID:5699 DOID:5699]

|

|

|

|-

| kidney osteogenic sarcoma

| class of disease

| kidney sarcoma
extraosseous osteosarcoma

| kidney sarcoma that starts in the bones and that is located in the kidney

| [http://www.disease-ontology.org/?id=DOID:5983 DOID:5983]

|

|

|

|-

| kidney papillary necrosis

| class of disease

| kidney disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2981 DOID:2981]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.419.493 C12.777.419.493]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.419.493 C13.351.968.419.493]

|

|

|-

| kidney pelvis papillary carcinoma

| class of disease

| renal pelvis transitional cell carcinoma
renal pelvis papillary tumor
papillary transitional carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5973 DOID:5973]

|

|

|

|-

| kidney pelvis sarcomatoid transitional cell carcinoma

| class of disease

| sarcomatoid transitional cell carcinoma
transitional cell carcinoma
renal pelvis carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6844 DOID:6844]

|

|

|

|-

| kidney rhabdoid cancer

| class of disease

| rhabdoid tumor
kidney sarcoma

| embryonal cancer that is located in the kidney

| [http://www.disease-ontology.org/?id=DOID:3674 DOID:3674]

|

|

|

|-

| kidney sarcoma

| class of disease

| kidney cancer
sarcoma

| kidney cancer that is located in the kidney's connective tissue

| [http://www.disease-ontology.org/?id=DOID:4242 DOID:4242]

|

|

|

|-

| klebsiellosis

| class of disease

| bacterial pneumonia
Enterobacteriaceae infectious disease

| infection by Klebsiella bacteria

| [http://www.disease-ontology.org/?id=DOID:13272 DOID:13272]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.400.310.503 C01.150.252.400.310.503]

|

|

|-

| kleptomania

| class of disease

| impulse control disorder
disease

| inability to resist the urge to steal

| [http://www.disease-ontology.org/?id=DOID:12400 DOID:12400]

|

| Kleptomania

| File:Constant Wauters Der ertappte Hausdiener.jpg

|-

| kwashiorkor

| class of disease

| protein-energy malnutrition
disease
dystrophy
protein deficiency

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13579 DOID:13579]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.654.521.719.500 C18.654.521.719.500]

| Kwashiorkor

| File:Kwashiorkor 6180.jpg

|-

| kyphoscoliotic heart disease

| class of disease

| chronic pulmonary heart disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12325 DOID:12325]

|

|

|

|-

| labia majora carcinoma

| class of disease

| vulva carcinoma
skin cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13389 DOID:13389]

|

|

|

|-

| labia minora cancer

| class of disease

| vulvar cancer
skin cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1243 DOID:1243]

|

|

|

|-

| labia minora carcinoma

| class of disease

| vulva carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1293 DOID:1293]

|

|

|

|-

| labium majus cancer

| class of disease

| vulvar cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11905 DOID:11905]

|

|

|

|-

| labyrinthine bilateral reactive loss

| class of disease

| labyrinthine dysfunction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14413 DOID:14413]

|

|

|

|-

| labyrinthine unilateral reactive loss

| class of disease

| labyrinthine dysfunction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1776 DOID:1776]

|

|

|

|-

| labyrinthitis

| class of disease

| otitis interna
inner ear disease
labyrinthosis
disease

| inflammation of the labyrinth, fluid-filled channels in the inner ear

| [http://www.disease-ontology.org/?id=DOID:1468 DOID:1468]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.218.568.558 C09.218.568.558]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.218.705.371 C09.218.705.371]

|

|

|-

| lacrimal apparatus disease

| class of disease

| eye disease
eye adnexa disease
rare palpebral, lacrimal system and conjunctival disease
rare genetic palpebral, lacrimal system and conjunctival disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1400 DOID:1400]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.496 C11.496]

|

|

|-

| lacrimal duct cancer

| class of disease

| lacrimal system cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12756 DOID:12756]

|

|

|

|-

| lacrimal duct obstruction

| class of disease

| lacrimal apparatus disease
stenosis and insufficiency of lacrimal passage

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13929 DOID:13929]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.496.456 C11.496.456]

| Nasolacrimal duct obstruction

| File:Tear system.svg

|-

| lacrimal gland adenocarcinoma

| class of disease

| lacrimal gland carcinoma
adenocarcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:298 DOID:298]

|

|

|

|-

| lacrimal gland cancer

| class of disease

| lacrimal system cancer
lacrimal gland neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:294 DOID:294]

|

|

|

|-

| lacrimal gland carcinoma

| class of disease

| lacrimal gland cancer
carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:293 DOID:293]

|

|

|

|-

| lacrimal passage granuloma

| class of disease

| lacrimal apparatus disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10174 DOID:10174]

|

|

|

|-

| lacrimal system cancer

| class of disease

| ocular cancer
lacrimal apparatus disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:292 DOID:292]

|

|

|

|-

| lactic acidosis

| class of disease

| acidosis
metabolic acidosis
disease

| acquired metabolic condition that has material basis in low pH in body tissues and blood accompanied by the buildup of lactate especially D-lactate

| [http://www.disease-ontology.org/?id=DOID:3650 DOID:3650]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.076.176.180 C18.452.076.176.180]

| Lactic acidosis

|

|-

| lactose intolerance

| class of disease

| carbohydrate metabolic disorder
malabsorption
food intolerance
disease

| condition involving a decreased ability to digest lactose due to a lack of lactase in the small intestines, either genetically or from injury

| [http://www.disease-ontology.org/?id=DOID:10604 DOID:10604]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.637.506 C06.405.469.637.506]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.202.589 C16.320.565.202.589]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.603.506 C18.452.603.506]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.202.589 C18.452.648.202.589]

| Lactose intolerance

| File:Lactose(lac).png

|-

| lambda 5 deficiency

| class of disease

| B cell deficiency
genetic disease
monogenic disease

| A B cell deficiency that has material basis in mutations in the IGLL1 gene. Lambda 5 mutations an cause a block in B cell development at the transition between the pro-B cell and the pre-B cell stage.

| [http://www.disease-ontology.org/?id=DOID:0060024 DOID:0060024]

|

|

|

|-

| language disorder

| class of disease

| communication disorder

| range of neurodevelopmental conditions

| [http://www.disease-ontology.org/?id=DOID:93 DOID:93]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.606.150.500 C10.597.606.150.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.604.150.500 C23.888.592.604.150.500]

|

|

|-

| large bowel leiomyoma

| class of disease

| intestinal benign neoplasm
leiomyoma
benign neoplasm of large intestine

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5143 DOID:5143]

|

|

|

|-

| large cell carcinoma

| class of disease

| carcinoma

| carcinoma that is composed of large, monotonous rounded or overtly polygonal-shaped cells with abundant cytoplasm

| [http://www.disease-ontology.org/?id=DOID:4552 DOID:4552]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.260 C04.557.470.200.260]

|

|

|-

| large cell carcinoma with rhabdoid phenotype

| class of disease

| large-cell lung carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7480 DOID:7480]

|

|

|

|-

| large cell keratinizing variant squamous cell breast carcinoma

| class of disease

| breast squamous cell carcinoma
keratinizing squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7461 DOID:7461]

|

|

|

|-

| large cell medulloblastoma

| class of disease

| medulloblastoma

| medulloblastoma that is characterized by cells that are larger than would be normally expected

| [http://www.disease-ontology.org/?id=DOID:3857 DOID:3857]

|

|

|

|-

| large cell neuroendocrine carcinoma

| class of disease

| large cell carcinoma
neuroendocrine carcinoma
large-cell lung carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050872 DOID:0050872]

|

| Large cell neuroendocrine carcinoma

|

|-

| large cell neuroendocrine carcinoma of the lung

| class of disease

| large cell neuroendocrine carcinoma
large-cell lung carcinoma
pulmonary neuroendocrine tumor

| human disease

| [http://www.disease-ontology.org/?id=DOID:6658 DOID:6658]

|

|

|

|-

| large intestine adenocarcinoma

| class of disease

| large intestine cancer
adenocarcinoma

| large intestine cancer that has material basis in epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:0050913 DOID:0050913]

|

|

|

|-

| large intestine adenoma

| class of disease

| intestinal benign neoplasm
gastrointestinal adenoma
benign neoplasms by histologic type

| intestinal benign neoplasm that has material basis in epithelial tissue with glandular origin and is located in the large intestine

| [http://www.disease-ontology.org/?id=DOID:0050914 DOID:0050914]

|

|

|

|-

| large intestine cancer

| class of disease

| intestinal cancer
colorectal neoplasm

| intestinal cancer that effects the long, tube-like organ that is connected to the small intestine at one end and the anus at the other

| [http://www.disease-ontology.org/?id=DOID:5672 DOID:5672]

|

|

|

|-

| large intestine lipoma

| class of disease

| intestinal benign neoplasm
lipoma
benign neoplasm of large intestine

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6460 DOID:6460]

|

|

|

|-

| large-cell acanthoma

| class of disease

| acanthoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4321 DOID:4321]

|

|

|

|-

| large-cell lung carcinoma

| class of disease

| non-small-cell lung carcinoma
large cell carcinoma
disease

| Disease

| [http://www.disease-ontology.org/?id=DOID:4556 DOID:4556]

|

| Large-cell lung carcinoma

|

|-

| large-cell lymphoma

| class of disease

| lymphatic system cancer
non-Hodgkin lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8538 DOID:8538]

|

|

|

|-

| laryngeal adenoid cystic carcinoma

| class of disease

| laryngeal carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4869 DOID:4869]

|

|

|

|-

| laryngeal cancer

| class of disease

| head and neck cancer
carcinoma
laryngeal neoplasm
respiratory system cancer
disease

| respiratory system cancer that is located in the larynx

| [http://www.disease-ontology.org/?id=DOID:2596 DOID:2596]

|

| Laryngeal cancer

| File:Tumor Laryngis-01.jpg

|-

| laryngeal carcinoma

| class of disease

| laryngeal cancer
carcinoma

| larynx cancer that has material basis in epithelial cells

| [http://www.disease-ontology.org/?id=DOID:2600 DOID:2600]

|

|

|

|-

| laryngeal cartilage cancer

| class of disease

| laryngeal cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13348 DOID:13348]

|

|

|

|-

| laryngeal disease

| class of disease

| upper respiratory tract disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:786 DOID:786]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.360 C08.360]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.400 C09.400]

|

|

|-

| laryngeal mucoepidermoid carcinoma

| class of disease

| mucoepidermoid carcinoma
laryngeal cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4688 DOID:4688]

|

|

|

|-

| laryngeal neoplasm

| class of disease

| respiratory tract neoplasm
laryngeal disease
neoplasm
respiratory system benign neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:2598 DOID:2598]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.443.665.481 C04.588.443.665.481]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.360.369 C08.360.369]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.785.481 C08.785.481]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.400.369 C09.400.369]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.647.481 C09.647.481]

| Neoplasms of larynx

|

|-

| laryngitis

| class of disease
symptom or sign

| laryngeal disease
inflammatory disease
throat symptom
disease

| inflammation of the larynx

| [http://www.disease-ontology.org/?id=DOID:3437 DOID:3437]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.360.535 C08.360.535]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.730.368 C08.730.368]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.400.535 C09.400.535]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.748.368 C01.748.368]

| Laryngitis

| File:Laryngitis gastrica.jpg

|-

| laryngostenosis

| class of disease

| laryngeal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11527 DOID:11527]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.360.591 C08.360.591]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.400.591 C09.400.591]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.740.658 C16.131.740.658]

|

|

|-

| laryngotracheitis

| class of disease
symptom or sign

| upper respiratory tract disease
throat symptom

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050148 DOID:0050148]

|

|

|

|-

| larynx carcinoma in situ

| class of disease

| laryngeal disease
in situ carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9011 DOID:9011]

|

|

|

|-

| larynx leiomyoma

| class of disease

| laryngeal neoplasm
leiomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10070 DOID:10070]

|

|

|

|-

| larynx leiomyosarcoma

| class of disease

| leiomyosarcoma

| larynx sarcoma that is a smooth muscle connective tissue tymor located in the larynx

| [http://www.disease-ontology.org/?id=DOID:5288 DOID:5288]

|

|

|

|-

| larynx liposarcoma

| class of disease

| liposarcoma
laryngeal cancer

| liposarcoma that is located in the larynx

| [http://www.disease-ontology.org/?id=DOID:5696 DOID:5696]

|

|

|

|-

| larynx sarcoma

| class of disease

| laryngeal cancer
sarcoma

| larynx cancer that has material basis in abnormally proliferating cells derived from embryonic mesoderm

| [http://www.disease-ontology.org/?id=DOID:2877 DOID:2877]

|

|

|

|-

| larynx squamous papilloma

| class of disease

| laryngeal neoplasm
squamous cell papilloma
laryngeal papillomatosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10071 DOID:10071]

|

|

|

|-

| late congenital syphilis

| class of disease

| congenital syphilis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10039 DOID:10039]

|

|

|

|-

| late yaws

| class of disease

| yaws

| yaws that appears after five years of the initial infection and is characterized by disabling consequences of the nose, bones and palmar/plantar hyperkeratosis

| [http://www.disease-ontology.org/?id=DOID:10567 DOID:10567]

|

|

|

|-

| late-adult onset retinitis pigmentosa

| class of disease

| retinitis pigmentosa
autosomal recessive disease

| retinitis pigmentosa that is characterized by onset of symptoms in the fifth or sixth decade of life

| [http://www.disease-ontology.org/?id=DOID:0110421 DOID:0110421]

|

|

|

|-

| lateral cystocele

| class of disease

| pelvic organ prolapse
cystocele

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14130 DOID:14130]

|

|

|

|-

| lateral displacement of eye

| class of disease

| orbital disease
exophthalmos

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12360 DOID:12360]

|

|

|

|-

| lateral medullary syndrome

| class of disease

| brain stem infarction

| neurological disorder causing a range of symptoms due to ischemia in the lateral part of the medulla oblongata in the brainstem

| [http://www.disease-ontology.org/?id=DOID:3522 DOID:3522]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.150.477.100.500 C10.228.140.300.150.477.100.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.775.200.100.500 C10.228.140.300.775.200.100.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.092.477.100.500 C14.907.253.092.477.100.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.855.200.100.500 C14.907.253.855.200.100.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.513.355.250.100.500 C23.550.513.355.250.100.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.717.489.250.100.500 C23.550.717.489.250.100.500]

| Lateral medullary syndrome

| File:WallenbergInfarct001.jpg

|-

| lateral myocardial infarction

| class of disease

| myocardial infarction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5853 DOID:5853]

|

|

|

|-

| lateral sinus thrombosis

| class of disease

| cerebral venous sinus thrombosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3574 DOID:3574]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.525.425.500.562 C10.228.140.300.525.425.500.562]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.566.350.500.562 C14.907.253.566.350.500.562]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.355.590.213.350.500.562 C14.907.355.590.213.350.500.562]

|

|

|-

| lateral ventricle meningioma

| class of disease

| intraventricular meningioma
cerebral meningioma
cerebral ventricle cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6115 DOID:6115]

|

|

|

|-

| latex allergy

| class of disease

| allergy
hazard
disease

| hypersensitivity reaction type I disease triggered by latex

| [http://www.disease-ontology.org/?id=DOID:0060532 DOID:0060532]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.600 C20.543.600]

|

|

|-

| learning disability

| class of disease

| specific developmental disorder
disability
disease

| range of neurodevelopmental conditions

| [http://www.disease-ontology.org/?id=DOID:8927 DOID:8927]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.606.150.550 C10.597.606.150.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.604.150.550 C23.888.592.604.150.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.625.562 F03.625.562]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.625.374.188 F03.625.374.188]

| Learning disabilities

|

|-

| leech infestation

| class of disease

| ectoparasitism
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:11079 DOID:11079]

|

|

|

|-

| leg dermatosis

| class of disease

| skin disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3142 DOID:3142]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.446 C17.800.446]

|

|

|-

| legionellosis

| class of disease

| primary bacterial infectious disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10458 DOID:10458]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.400.500 C01.150.252.400.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.730.382 C08.730.382]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.748.382 C01.748.382]

|

|

|-

| legume allergy

| class of disease

| fruit allergy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060904 DOID:0060904]

|

|

|

|-

| leiomyoma

| class of disease

| benign neoplasms by histologic type
smooth muscle tumour
myoma
disease

| cell type benign neoplasm that is a benign tumor of smooth muscle cells

| [http://www.disease-ontology.org/?id=DOID:127 DOID:127]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.590.450 C04.557.450.590.450]

| Leiomyomas

| File:Leiomyoma Uterus 40x.jpg

|-

| leiomyoma cutis

| class of disease

| dermis tumor
skin benign neoplasm
leiomyoma

| benign tumor that arises from smooth muscle tissue in a hair follicle, forming a papule

| [http://www.disease-ontology.org/?id=DOID:5132 DOID:5132]

|

| Cutaneous leiomyoma

|

|-

| leiomyomatosis

| class of disease

| leiomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5138 DOID:5138]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.590.450.465 C04.557.450.590.450.465]

|

|

|-

| leiomyosarcoma

| class of disease

| smooth muscle cancer
disease

| malignant smooth muscle cancer that can arise almost anywhere in the body, but is most common in the uterus, abdomen, or pelvis

| [http://www.disease-ontology.org/?id=DOID:1967 DOID:1967]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.590.455 C04.557.450.590.455]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.455 C04.557.450.795.455]

| Leiomyosarcoma

| File:Cutaneous leiomyosarcoma - high mag.jpg

|-

| lens disease

| class of disease

| eye disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:110 DOID:110]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.510 C11.510]

|

|

|-

| lens subluxation

| class of disease

| lens disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11364 DOID:11364]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.510.598 C11.510.598]

|

|

|-

| lens-induced iridocyclitis

| class of disease

| iridocyclitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9388 DOID:9388]

|

|

|

|-

| leptomeninges sarcoma

| class of disease

| malignant leptomeningeal tumor
meninges sarcoma
sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7689 DOID:7689]

|

|

|

|-

| lesion of sciatic nerve

| class of disease

| mononeuritis of lower limb

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12528 DOID:12528]

|

|

|

|-

| lethal congenital contracture syndrome 1

| class of disease

| lethal congenital contracture syndrome
genetic disease

| lethal congenital contracture syndrome that has material basis in homozygous or compound heterozygous mutation in the mRNA export mediator GLE1 on chromosome 9q34

| [http://www.disease-ontology.org/?id=DOID:0060559 DOID:0060559]

|

|

|

|-

| leucine-sensitive hypoglycemia of infancy

| class of disease

| amino acid metabolic disorder
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112262 DOID:0112262]

|

|

|

|-

| leukemia

| class of disease
symptom or sign

| hematologic cancer
myeloproliferative disorders
disease

| group of cancers that usually begin in the bone marrow

| [http://www.disease-ontology.org/?id=DOID:1240 DOID:1240]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337 C04.557.337]

| Leukemias

| File:Symptoms of leukemia.png

|-

| leukocoria

| class of disease

| pupil disorder
eye degenerative disease

| abnormal white reflection from the retina of the eye

| [http://www.disease-ontology.org/?id=DOID:11772 DOID:11772]

|

| Leukocoria

| File:Rb whiteeye.PNG

|-

| leukocyte adhesion deficiency 2

| class of disease

| leukocyte adhesion deficiency 3

| leukocyte adhesion deficiency that is characterized by recurrent bacterial infections, severe growth delay and severe intellectual deficit

| [http://www.disease-ontology.org/?id=DOID:0080492 DOID:0080492]

|

|

|

|-

| leukocyte disease

| class of disease
symptom or sign

| hematopoietic system disease

| disease involving the leukocyte

| [http://www.disease-ontology.org/?id=DOID:9500 DOID:9500]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.553 C15.378.553]

| Leukocyte disorders

|

|-

| leukodystrophy

| class of disease

| cerebral degeneration
disease

| cerebral degeneration characterized by dysfunction of the white matter of the brain

| [http://www.disease-ontology.org/?id=DOID:10579 DOID:10579]

|

| Leukodystrophies

|

|-

| leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome

| class of disease

| nervous system heredodegenerative disease
combined oxidative phosphorylation deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111493 DOID:0111493]

|

|

|

|-

| leukopenia

| class of disease
symptom or sign

| leukocyte disease
cytopenia
hemic system symptom
disease

| decrease in the number of white blood cells

| [http://www.disease-ontology.org/?id=DOID:615 DOID:615]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.553.546 C15.378.553.546]

|

|

|-

| leukoplakia of penis

| class of disease

| penile disease
leukoplakia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8738 DOID:8738]

|

|

|

|-

| leukoplakia of vagina

| class of disease

| vaginal disease
leukoplakia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8920 DOID:8920]

|

|

|

|-

| leukorrhea

| class of disease

| vaginal discharge
disease

| type of vaginal discharge

| [http://www.disease-ontology.org/?id=DOID:3766 DOID:3766]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.894.700.500 C13.351.500.894.700.500]

|

|

|-

| leukostasis

| class of disease

| leukocyte disease
leukocytosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:12986 DOID:12986]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.553.560 C15.378.553.560]

|

|

|-

| lichen disease

| class of disease

| skin disease
lichenoid eruption

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8574 DOID:8574]

|

|

|

|-

| lichen nitidus

| class of disease

| lichen disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8573 DOID:8573]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.859.475.545 C17.800.859.475.545]

| Lichen nitidus

|

|-

| lichen planus

| class of disease

| lichen disease
disease

| chronic disease of skin, tongue or oral mucosa

| [http://www.disease-ontology.org/?id=DOID:9201 DOID:9201]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.859.475.560 C17.800.859.475.560]

| Lichen planus

| File:Lichen planus lip.jpg

|-

| lidocaine allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger lidocaine

| [http://www.disease-ontology.org/?id=DOID:0040009 DOID:0040009]

|

|

|

|-

| limb ischemia

| class of disease

| ischemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050852 DOID:0050852]

|

| Limb ischemia

|

|-

| limb-girdle muscular dystrophy

| class of disease

| muscular dystrophy
progressive muscular dystrophy
disease

| muscular dystrophy characterized by weakening of the muscles of the hip and shoulders which comprise the limb girdle muscles

| [http://www.disease-ontology.org/?id=DOID:11724 DOID:11724]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.534.500.280 C05.651.534.500.280]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.491.175.500.149 C10.668.491.175.500.149]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.577.280 C16.320.577.280]

|

|

|-

| limbic encephalitis

| class of disease

| paraneoplastic neurologic syndrome
encephalitis
inflammatory and autoimmune disease with epilepsy
autoimmune disease of the nervous system

| Inflammation involving the limbic system in the brain

| [http://www.disease-ontology.org/?id=DOID:0080741 DOID:0080741]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.614.550.450 C04.588.614.550.450]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.730.856.437 C04.730.856.437]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.430.525 C10.228.140.430.525]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.228.245.700 C10.228.228.245.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.781.550 C10.574.781.550]

|

|

|-

| limited scleroderma

| class of disease

| systemic scleroderma

| the least progressive form of systemic scleroderma with skin thickening restricted to the face, neck and areas distal to the elbows and/or knees, sparing the trunk

| [http://www.disease-ontology.org/?id=DOID:1577 DOID:1577]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.799.801 C17.300.799.801]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.784.801 C17.800.784.801]

|

|

|-

| linear skin defects with multiple congenital anomalies 1

| class of disease

| microphthalmia–dermal aplasia–sclerocornea syndrome
X-linked dominant disease
congenital disorder

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111808 DOID:0111808]

|

|

|

|-

| lingual goiter

| class of disease

| goiter

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13196 DOID:13196]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.894.500.500 C16.131.894.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.874.283.802 C19.874.283.802]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.874.689.500.500 C19.874.689.500.500]

|

|

|-

| lingual-facial-buccal dyskinesia

| class of disease

| movement disorders

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9854 DOID:9854]

|

|

|

|-

| linitis plastica

| class of disease

| gastric diffuse adenocarcinoma
stomach carcinoma
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4023 DOID:4023]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.095.410 C04.557.470.200.025.095.410]

| Linitis plastica

|

|-

| lip disease

| class of disease

| mouth disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:9297 DOID:9297]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.409 C07.465.409]

| Lip disorders

|

|-

| lipid metabolism disorder

| class of disease

| inherited metabolic disorder
disease

| high cholesterol & lipids

| [http://www.disease-ontology.org/?id=DOID:3146 DOID:3146]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584 C18.452.584]

| Dyslipidemia

| File:Fig21Femme obese.jpg

|-

| lipid storage disease

| class of disease

| lysosomal storage disease
disease

| lysosomal storage disease that involves the accumulation of harmful amounts of lipids (fats) in some of the body's cells and tissues

| [http://www.disease-ontology.org/?id=DOID:9455 DOID:9455]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.398.641 C16.320.565.398.641]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.563.641 C18.452.584.563.641]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.398.641 C18.452.648.398.641]

| Lipid storage disorders

|

|-

| lipid-cell variant infiltrating bladder urothelial carcinoma

| class of disease

| invasive bladder transitional cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7967 DOID:7967]

|

|

|

|-

| lipid-rich breast carcinoma

| class of disease

| lipid-rich carcinoma
bilateral breast cancer

| lipid-rich carcinoma characterized by the presence of cytoplasmic neutral lipids in the vast majority of the malignant cells

| [http://www.disease-ontology.org/?id=DOID:7076 DOID:7076]

|

|

|

|-

| lipid-rich carcinoma

| class of disease

| breast carcinoma

| breast carcinoma characterized by the presence of malignant epithelial cells with clear cytoplasm which contains neutral lipids

| [http://www.disease-ontology.org/?id=DOID:5658 DOID:5658]

|

|

|

|-

| lipoadenoma

| class of disease

| adenoma

| adenoma that is composed of adipose tissue

| [http://www.disease-ontology.org/?id=DOID:5398 DOID:5398]

|

|

|

|-

| lipoatrophic diabetes

| class of disease

| type 2 diabetes

| type 2 diabetes that involves severe lipodystrophy in addition to the traditional signs of diabetes

| [http://www.disease-ontology.org/?id=DOID:11712 DOID:11712]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.394.750.149.500 C18.452.394.750.149.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.246.300.500 C19.246.300.500]

|

|

|-

| lipoid nephrosis

| class of disease

| idiopathic nephrotic syndrome
nephrotic syndrome
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10966 DOID:10966]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.419.630.477 C12.777.419.630.477]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.419.630.477 C13.351.968.419.630.477]

| Minimal change disease

|

|-

| lipoma

| class of disease

| benign neoplasms by histologic type
adipose tissue neoplasm
disease

| benign tumor made of fat tissue

| [http://www.disease-ontology.org/?id=DOID:3315 DOID:3315]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.550.400 C04.557.450.550.400]

| Lipomas

| File:Lipoma 02.jpg

|-

| lipoma of colon

| class of disease

| large intestine lipoma
colonic disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10655 DOID:10655]

|

|

|

|-

| lipoma of spermatic cord

| class of disease

| paratesticular lipoma
lipoma
male reproductive organ benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10206 DOID:10206]

|

|

|

|-

| lipoma of the rectum

| class of disease

| large intestine lipoma
benign neoplasm of rectum

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6459 DOID:6459]

|

|

|

|-

| lipomatosis

| class of disease

| skin disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3153 DOID:3153]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.463 C17.800.463]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.718 C18.452.584.718]

| Lipomatosis

|

|-

| liposarcoma

| class of disease

| lipomatous cancer
sarcoma
disease

| lipomatous cancer that arises in fat cells in deep soft tissue retroperitoneum

| [http://www.disease-ontology.org/?id=DOID:3382 DOID:3382]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.550.420 C04.557.450.550.420]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.465 C04.557.450.795.465]

| Liposarcoma

| File:Myxoid liposarcoma (06).JPG

|-

| liposarcoma of bone

| class of disease

| osteosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3381 DOID:3381]

|

|

|

|-

| liposarcoma of the ovary

| class of disease

| ovary sarcoma
liposarcoma
sarcoma
ovarian cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5697 DOID:5697]

|

|

|

|-

| lissencephaly 3

| class of disease

| autosomal dominant disease
lissencephaly

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112232 DOID:0112232]

|

|

|

|-

| liver angiosarcoma

| class of disease

| angiosarcoma
liver cancer
hepatic vascular disease
liver sarcoma
organ type

| angiosarcoma and sarcoma of liver and hemangioma of intra-abdominal structure and Ca liver - primary that is located in the liver

| [http://www.disease-ontology.org/?id=DOID:268 DOID:268]

|

| Liver angiosarcoma

| File:Gross specimen of liver angiosarcoma.jpg

|-

| liver cancer

| class of disease

| liver tumor
liver disease
rare hepatic and biliary tract tumor
liver neoplasm
hepatobiliary system cancer
endocrine gland cancer
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3571 DOID:3571]

|

| Liver cancer

| File:Liver Cancer in Mouse Model (42507312762).jpg

|-

| liver carcinoma

| class of disease

| liver cancer
carcinoma

| liver cancer that has material basis in epithelial cells

| [http://www.disease-ontology.org/?id=DOID:686 DOID:686]

|

|

|

|-

| liver carcinoma in situ

| class of disease

| in situ carcinoma
liver disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9132 DOID:9132]

|

|

|

|-

| liver cirrhosis

| class of disease

| liver disease
cirrosis
disease

| chronic disease of the liver, characterized by fibrosis

| [http://www.disease-ontology.org/?id=DOID:5082 DOID:5082]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.630 C06.552.630]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.355.412 C23.550.355.412]

| Cirrhosis

| File:Liver Cirrhosis.png

|-

| liver disease

| class of disease

| hepatobiliary disease
endocrine system disease
disease

| disorder of the human liver

| [http://www.disease-ontology.org/?id=DOID:409 DOID:409]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552 C06.552]

| Diseases and disorders of liver

|

|-

| liver fibroma

| class of disease

| liver neoplasm
fibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:907 DOID:907]

|

|

|

|-

| liver fibrosarcoma

| class of disease

| liver sarcoma
fibrosarcoma

| fibrosarcoma of soft tissue and sarcoma of liver that is located in the liver

| [http://www.disease-ontology.org/?id=DOID:8022 DOID:8022]

|

|

|

|-

| liver inflammatory pseudotumor

| class of disease

| Inflammatory pseudotumor
inflammatory myofibroblastic tumour
rare hepatic disease
liver neoplasm
rare hepatic and biliary tract tumor
endocrine gland cancer
liver disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:918 DOID:918]

|

|

|

|-

| liver leiomyoma

| class of disease

| liver neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:917 DOID:917]

|

|

|

|-

| liver leiomyosarcoma

| class of disease

| liver sarcoma

| leiomyosarcoma and sarcoma of liver that is located in the liver

| [http://www.disease-ontology.org/?id=DOID:5296 DOID:5296]

|

|

|

|-

| liver lipoma

| class of disease

| liver neoplasm
gastrointestinal system benign neoplasm
endocrine organ benign neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:10190 DOID:10190]

|

|

|

|-

| liver lymphoma

| class of disease

| liver cancer
endocrine gland cancer
gastrointestinal lymphoma
rare hepatic disease
lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:901 DOID:901]

|

|

|

|-

| liver neoplasm

| class of disease

| liver tumor
hepatobiliary neoplasm
liver disease
endocrine organ benign neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:916 DOID:916]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.623 C04.588.274.623]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.623 C06.301.623]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.697 C06.552.697]

| Benign neoplasms of liver

|

|-

| liver rhabdomyosarcoma

| class of disease

| liver sarcoma

| rhabdomyosarcoma and sarcoma of liver that are located in the liver

| [http://www.disease-ontology.org/?id=DOID:4047 DOID:4047]

|

|

|

|-

| liver sarcoma

| class of disease

| liver cancer

| sarcoma and malignant non-epithelial hepatic and intrahepatic bile duct neoplasm sthat is located in the liver

| [http://www.disease-ontology.org/?id=DOID:270 DOID:270]

|

|

|

|-

| lobomycosis

| class of disease

| dermatomycosis
disease

| dermatomycosis that results in infection located in skin or located in subcutaneous tissue, has material basis in Lacazia loboi and has symptom crusty plaques, has symptom tumors and results in formation of nodular lesions

| [http://www.disease-ontology.org/?id=DOID:13026 DOID:13026]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.800.200.475 C01.800.200.475]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.703.302.475 C01.150.703.302.475]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.838.208.475 C17.800.838.208.475]

| Lobomycosis

|

|-

| lobular neoplasia

| class of disease

| breast carcinoma in situ
breast neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3010 DOID:3010]

|

|

|

|-

| localized anterior staphyloma

| class of disease

| scleral staphyloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13787 DOID:13787]

|

|

|

|-

| localized chondrosarcoma

| class of disease

| chondrosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5862 DOID:5862]

|

|

|

|-

| localized osteosarcoma

| class of disease

| osteosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3356 DOID:3356]

|

|

|

|-

| localized pulmonary fibrosis

| class of disease

| pulmonary fibrosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5642 DOID:5642]

|

|

|

|-

| localized scleroderma

| class of disease

| scleroderma

| human disease

| [http://www.disease-ontology.org/?id=DOID:8472 DOID:8472]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.787 C17.300.787]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.767 C17.800.767]

| Morphea

| File:MercMorphea.JPG

|-

| locked-in syndrome

| class of disease

| neurological disorder
disease

| condition in which a patient is aware but cannot move or communicate verbally due to complete paralysis of nearly all voluntary muscles in the body except for vertical eye movements and blinking

| [http://www.disease-ontology.org/?id=DOID:12697 DOID:12697]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.622.760.500 C10.597.622.760.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.416 C10.668.416]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.636.786.500 C23.888.592.636.786.500]

|

| File:CerebellumArteries.jpg

|-

| long QT syndrome 1

| class of disease

| long QT syndrome
genetic disease
autosomal dominant disease

| A long QT syndrome that has material basis in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4.

| [http://www.disease-ontology.org/?id=DOID:0110644 DOID:0110644]

|

|

|

|-

| long QT syndrome 10

| class of disease

| long QT syndrome
genetic disease
autosomal dominant disease

| A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3.

| [http://www.disease-ontology.org/?id=DOID:0110651 DOID:0110651]

|

|

|

|-

| long QT syndrome 4

| class of disease

| long QT syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111701 DOID:0111701]

|

|

|

|-

| long bone adamantinoma

| class of disease

| adamantinoma

| adamantinoma that is located in the long bones and results in focal epithelial differentiation

| [http://www.disease-ontology.org/?id=DOID:2775 DOID:2775]

|

|

|

|-

| long bones of lower limb cancer

| class of disease

| bone cancer
lower limb cancer

| bone cancer that is manifested in the long bones of the lower limb

| [http://www.disease-ontology.org/?id=DOID:10149 DOID:10149]

|

|

|

|-

| loose anagen syndrome

| class of disease

| alopecia
baldness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111702 DOID:0111702]

|

|

|

|-

| low compliance bladder

| class of disease

| bladder disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:12144 DOID:12144]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.829.866 C12.777.829.866]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.829.813 C13.351.968.829.813]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.942.343.780 C23.888.942.343.780]

|

|

|-

| low grade glioma

| class of disease

| glioma

| A grade I or grade II glioma arising from the central nervous system. This category includes pilocytic astrocytoma, diffuse astrocytoma, subependymal giant cell astrocytoma, ependymoma, oligodendroglioma, oligoastrocytoma, and angiocentric glioma.

| [http://www.disease-ontology.org/?id=DOID:0080829 DOID:0080829]

|

|

|

|-

| low implantation of placenta

| class of disease

| placenta praevia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1677 DOID:1677]

|

|

|

|-

| low tension glaucoma

| class of disease

| open-angle glaucoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13544 DOID:13544]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.640.225 C11.640.225]

|

|

|-

| lower respiratory tract disease

| class of disease

| respiratory disease

| respiratory system disease which involves the lower respiratory tract

| [http://www.disease-ontology.org/?id=DOID:0050161 DOID:0050161]

|

|

|

|-

| lumbar plexus neoplasm

| class of disease

| nerve plexus neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8389 DOID:8389]

|

|

|

|-

| lumbar spinal canal and spinal cord meningioma

| class of disease

| spinal canal and spinal cord meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7515 DOID:7515]

|

|

|

|-

| lumbosacral lipoma

| class of disease

| bone benign neoplasm
lipoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7017 DOID:7017]

|

|

|

|-

| lumbosacral plexus lesion

| class of disease

| peripheral neuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13913 DOID:13913]

|

|

|

|-

| luminal breast carcinoma

| class of disease

| breast carcinoma
breast carcinoma by gene expression profile

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060548 DOID:0060548]

|

|

|

|-

| luminal breast carcinoma B

| class of disease

| breast carcinoma
luminal breast carcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080674 DOID:0080674]

|

|

|

|-

| lung acinar adenocarcinoma

| class of disease

| adenocarcinoma of the lung

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6482 DOID:6482]

|

|

|

|-

| lung adenoid cystic carcinoma

| class of disease

| lung carcinoma
adenoid cystic carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4872 DOID:4872]

|

|

|

|-

| lung adenoma

| class of disease

| lung benign neoplasm
benign epithelial neoplasm
benign neoplasms by histologic type
adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5386 DOID:5386]

|

|

|

|-

| lung benign neoplasm

| class of disease

| respiratory system benign neoplasm
lung disease
lung neoplasm
thoracic cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:3683 DOID:3683]

|

| Benign neoplasms of bronchus and lung

|

|-

| lung carcinoma

| class of disease

| lung cancer
carcinoma

| lung cancer that has material basis in abnormally proliferating cells derives from epithelial cells and is located in the lungs and has symptom cough and has symptom chest discomfort or pain and has symptom weight loss and has symptom hemoptysis

| [http://www.disease-ontology.org/?id=DOID:3905 DOID:3905]

|

|

|

|-

| lung carcinoma in situ

| class of disease

| in situ carcinoma
lung disease
lung neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8800 DOID:8800]

|

|

|

|-

| lung clear cell carcinoma

| class of disease

| clear cell carcinoma
lung carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7267 DOID:7267]

|

|

|

|-

| lung clear cell-sugar-tumor

| class of disease

| lung benign neoplasm
perivascular epithelioid cell neoplasm
benign perivascular tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5763 DOID:5763]

|

|

|

|-

| lung combined large cell neuroendocrine carcinoma

| class of disease

| large cell neuroendocrine carcinoma of the lung
combined carcinoma of lung

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7207 DOID:7207]

|

|

|

|-

| lung combined type small cell carcinoma

| class of disease

| lung small cell carcinoma
combined carcinoma of lung

| lung small cell carcinoma that is characterized as a multiphasic lung cancer comprised of a mixture of small cell and non-small cell lung carcinoma cells

| [http://www.disease-ontology.org/?id=DOID:5421 DOID:5421]

|

|

|

|-

| lung disease

| class of disease

| lower respiratory tract disease
disease

| respiratory disease

| [http://www.disease-ontology.org/?id=DOID:850 DOID:850]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381 C08.381]

|

|

|-

| lung hilum cancer

| class of disease

| lung cancer
hilar lung neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7696 DOID:7696]

|

|

|

|-

| lung leiomyoma

| class of disease

| lung benign neoplasm
leiomyoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5136 DOID:5136]

|

|

|

|-

| lung leiomyosarcoma

| class of disease

| leiomyosarcoma

| leiomyosarcoma and sarcoma of lung that is located in the lung

| [http://www.disease-ontology.org/?id=DOID:5265 DOID:5265]

|

|

|

|-

| lung lymphoma

| class of disease

| lung cancer
lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6760 DOID:6760]

|

|

|

|-

| lung meningioma

| class of disease

| lung cancer
malignant neoplasm of meninges
rare genetic respiratory disease
genetic nervous system disorder
ectopic meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5764 DOID:5764]

|

|

|

|-

| lung mixed small cell and squamous cell carcinoma

| class of disease

| pulmonary neuroendocrine tumor
lung combined type small cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7081 DOID:7081]

|

|

|

|-

| lung mucoepidermoid carcinoma

| class of disease

| lung carcinoma
mucoepidermoid carcinoma

| lung carcinoma that has material basis in a combination of squamous cells, mucus secreting cells and intermediate cells

| [http://www.disease-ontology.org/?id=DOID:0050932 DOID:0050932]

|

| Mucoepidermoid lung carcinoma

|

|-

| lung non-squamous non-small cell carcinoma

| class of disease

| non-small-cell lung carcinoma

| lung non-small cell carcinoma that is characterized by the lack of evidence of squamous differentiation

| [http://www.disease-ontology.org/?id=DOID:0080521 DOID:0080521]

|

|

|

|-

| lung oat cell carcinoma

| class of disease

| lung small cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5411 DOID:5411]

|

|

|

|-

| lung occult adenocarcinoma

| class of disease

| adenocarcinoma of the lung

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7168 DOID:7168]

|

|

|

|-

| lung occult large cell carcinoma

| class of disease

| large-cell lung carcinoma
lung occult non-small cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7169 DOID:7169]

|

|

|

|-

| lung occult small cell carcinoma

| class of disease

| lung small cell carcinoma
lung occult carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5414 DOID:5414]

|

|

|

|-

| lung occult squamous cell carcinoma

| class of disease

| squamous cell carcinoma of the lung
lung occult carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6510 DOID:6510]

|

|

|

|-

| lung papillary adenocarcinoma

| class of disease

| adenocarcinoma of the lung

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5588 DOID:5588]

|

|

|

|-

| lung sarcoma

| class of disease

| lung cancer
sarcoma

| lung cancer that is located in the lung and that arises from transformed cells of mesenchymal origin

| [http://www.disease-ontology.org/?id=DOID:2784 DOID:2784]

|

|

| File:Primary pulmonary sarcoma, NOS - Case 299 (15760799904).jpg

|-

| lung small cell carcinoma

| class of disease

| lung carcinoma
small cell carcinoma

| lung carcinoma that has material basis in primitive-appearing cells that are smaller than normal cells

| [http://www.disease-ontology.org/?id=DOID:5409 DOID:5409]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.894.797.520.109.220.624 C04.588.894.797.520.109.220.624]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.540.140.750 C08.381.540.140.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.785.520.100.220.750 C08.785.520.100.220.750]

|

| File:Combined small cell lung carcinoma with extensive mucosal involvement; possible SCLC in situ Case 271 (9255562385).jpg

|-

| lung superior sulcus carcinoma

| class of disease

| Pancoast tumor

| human disease

| [http://www.disease-ontology.org/?id=DOID:8208 DOID:8208]

|

|

|

|-

| lupus erythematosus

| class of disease

| autoimmune disease
autoimmune disease of musculoskeletal system
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:8857 DOID:8857]

|

|

| File:Butterflyrash.jpg

|-

| lupus nephritis

| class of disease

| glomerulonephritis
disease

| inflammation of the kidneys

| [http://www.disease-ontology.org/?id=DOID:0080162 DOID:0080162]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.777.419.570.363.680 C12.200.777.419.570.363.680]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.968.419.570.363.680 C12.050.351.968.419.570.363.680]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.480.680 C17.300.480.680]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.590.560 C20.111.590.560]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.950.419.570.363.680 C12.950.419.570.363.680]

| Lupus nephritis

|

|-

| luteoma

| class of disease

| ovarian benign neoplasm
ovarian disease
disease

| ovarian benign neoplasm characterized by solid proliferations of luteinized cells, resulting in a tumor-like ovarian enlargement that regresses during the puerperium

| [http://www.disease-ontology.org/?id=DOID:7880 DOID:7880]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.475.750.751 C04.557.475.750.751]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.455.464 C04.588.322.455.464]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.056.630.705.464 C13.351.500.056.630.705.464]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.937.418.685.464 C13.351.937.418.685.464]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.410.464 C19.344.410.464]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.630.705.464 C19.391.630.705.464]

| Luteoma of pregnancy

|

|-

| luxation of globe

| class of disease

| globe disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1241 DOID:1241]

|

|

|

|-

| lymph node adenoid cystic carcinoma

| class of disease

| lymph node metastasis
carcinoma
lymph node cancer
lymph node carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060219 DOID:0060219]

|

|

|

|-

| lymph node cancer

| class of disease

| lymphatic system cancer
lymph node neoplasm
lymph node disease

| lymphatic system cancer that is located in the lymph node

| [http://www.disease-ontology.org/?id=DOID:10619 DOID:10619]

|

| Lymph node cancers

|

|-

| lymph node carcinoma

| class of disease

| carcinoma
lymph node cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080618 DOID:0080618]

|

|

|

|-

| lymph node disease

| class of disease

| lymphatic system disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9942 DOID:9942]

|

| Diseases and disorders of lymph nodes

|

|-

| lymph node palisaded myofibroblastoma

| class of disease

| lymph node cancer
benign neoplasm of lymph node

| human disease

| [http://www.disease-ontology.org/?id=DOID:8304 DOID:8304]

|

|

|

|-

| lymphadenitis

| class of disease
symptom or sign

| lymph node disease
clinical sign
lymphatic system symptom
adenitis

| lymph node and lymph vessels inflammation

| [http://www.disease-ontology.org/?id=DOID:1602 DOID:1602]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.315 C15.604.315]

|

|

|-

| lymphangioma

| class of disease

| lymphatic system malformation
benign blood vessel neoplasm
disease

| malformations of the lymphatic system characterized by lesions that are thin-walled cysts

| [http://www.disease-ontology.org/?id=DOID:1475 DOID:1475]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.375.450 C04.557.375.450]

| Lymphangiomas

| File:Lymphangioma.jpg

|-

| lymphangiosarcoma

| class of disease

| lymphatic system cancer
angiosarcoma associated with lymphedema
skin carcinoma
skin sarcoma
disease

| lymphatic system cancer that has material basis in endothelial cells located in lymphatic vessels

| [http://www.disease-ontology.org/?id=DOID:2689 DOID:2689]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.375.480 C04.557.375.480]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.480 C04.557.450.795.480]

|

|

|-

| lymphatic system cancer

| class of disease

| immune system cancer
lymphatic system disease

| immune system cancer that is located in the lymphatic system and is characterized by uncontrolled cellular proliferation of lymphoid tissue

| [http://www.disease-ontology.org/?id=DOID:0060073 DOID:0060073]

|

|

|

|-

| lymphatic system disease

| class of disease

| immune disorder

| immune system disease that is located in the lymphatic system

| [http://www.disease-ontology.org/?id=DOID:75 DOID:75]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604 C15.604]

|

|

|-

| lymphoblastic leukemia

| class of disease

| leukemia

| leukemia that has material basis in lymphoblasts (immature white blood cells)

| [http://www.disease-ontology.org/?id=DOID:1037 DOID:1037]

|

|

|

|-

| lymphoblastic lymphoma

| class of disease
symptom or sign

| non-Hodgkin lymphoma
lymphoma
lymphatic system symptom

| lymphoma that has material basis in immature malignant lymphocytes (lymphoblasts) committed to the B-cell or T-cell lineage and located in primarily lymph nodes or located in extranodal sites

| [http://www.disease-ontology.org/?id=DOID:0080147 DOID:0080147]

|

|

|

|-

| lymphocele

| class of disease

| lymphatic system disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4347 DOID:4347]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.182.430 C04.182.430]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.510 C15.604.510]

|

|

|-

| lymphocytic gastritis

| class of disease

| gastritis
chronic gastritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4035 DOID:4035]

|

|

|

|-

| lymphoepithelioma-like acinar prostate adenocarcinoma

| class of disease

| prostate adenocarcinoma
prostatic acinar adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7246 DOID:7246]

|

|

|

|-

| lymphoepithelioma-like carcinoma

| class of disease

| carcinoma
large cell carcinoma

| carcinoma that is a malignant epithelial neoplasm densely infiltrated by lymphoid cells

| [http://www.disease-ontology.org/?id=DOID:5660 DOID:5660]

|

| Lymphoepithelioma-like carcinoma

|

|-

| lymphoepithelioma-like thymic carcinoma

| class of disease

| thymic carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7599 DOID:7599]

|

|

|

|-

| lymphohistiocytoid mesothelioma

| class of disease

| malignant pleural mesothelioma
sarcomatoid mesothelioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7381 DOID:7381]

|

|

|

|-

| lymphoid interstitial pneumonia

| class of disease

| idiopathic interstitial pneumonia
lymphoproliferative disorders

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050159 DOID:0050159]

|

|

|

|-

| lymphoma

| class of disease
symptom or sign

| hematologic cancer
lymphatic system cancer
lymphoma and pseudolymphoma
lymphoid neoplasm
disease

| hematologic cancer that affects lymphocytes

| [http://www.disease-ontology.org/?id=DOID:0060058 DOID:0060058]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386 C04.557.386]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.569 C15.604.515.569]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.761 C20.683.515.761]

| Lymphomas

| File:Gastric MALT lymphoma 2.jpg

|-

| lymphoma-like variant infiltrating bladder urothelial carcinoma

| class of disease

| invasive bladder transitional cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7972 DOID:7972]

|

|

|

|-

| lymphopenia

| class of disease
symptom or sign

| leukopenia
lymphatic system symptom
disease

| leukopenia that is the condition of having an abnormally low level of lymphocytes in the blood

| [http://www.disease-ontology.org/?id=DOID:614 DOID:614]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.553.546.605 C15.378.553.546.605]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.673.627 C20.673.627]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.243.750.605 C15.378.243.750.605]

|

|

|-

| lymphoplasmacyte-rich meningioma

| class of disease

| meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4591 DOID:4591]

|

|

|

|-

| lysosomal and lipase deficiency

| class of disease

| lipid storage disease

| lipid storage disease characterized by lysosomal and lipase deficiency

| [http://www.disease-ontology.org/?id=DOID:0080217 DOID:0080217]

|

|

|

|-

| macrocystic neurilemmoma

| class of disease

| neurilemmoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3203 DOID:3203]

|

|

|

|-

| macrocystic pattern testicular yolk sac tumor

| class of disease

| testicular yolk sac tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7097 DOID:7097]

|

|

|

|-

| macrocytic anemia

| class of disease
symptom or sign

| anemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2361 DOID:2361]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.252 C15.378.071.252]

|

|

|-

| macroglobulinemia

| class of disease

| plasma protein metabolism disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9080 DOID:9080]

|

|

|

|-

| macrotrabecular hepatoblastoma

| class of disease

| hepatoblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5798 DOID:5798]

|

|

|

|-

| macular degeneration

| class of disease

| retinal degeneration
maculopathy
blindness

| retinal degeneration characterized by gradual deterioration of light-sensing cells in the tissues at the back of the eye

| [http://www.disease-ontology.org/?id=DOID:4448 DOID:4448]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.768.585.439 C11.768.585.439]

| Macular degeneration

| File:Intermediate age related macular degeneration.jpg

|-

| macular hole

| class of disease

| retinal disease
retinal perforation
maculopathy

| small break in the macula, located in the center of the eye's light-sensitive tissue called the retina

| [http://www.disease-ontology.org/?id=DOID:7633 DOID:7633]

|

| Macular hole

|

|-

| macular keratitis

| class of disease

| keratitis

| human disease

| [http://www.disease-ontology.org/?id=DOID:11871 DOID:11871]

|

|

|

|-

| macular retinal edema

| class of disease

| retinal edema
maculopathy
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4449 DOID:4449]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.768.585.439.245 C11.768.585.439.245]

| Macular edema

|

|-

| main bronchus cancer

| class of disease

| lung cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3924 DOID:3924]

|

|

|

|-

| major depressive disorder

| class of disease

| depressive disorder
mental depression
disease

| all-encompassing low mood accompanied by low self-esteem, and by loss of interest or pleasure in normally enjoyable activities

| [http://www.disease-ontology.org/?id=DOID:1470 DOID:1470]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.600.300.375 F03.600.300.375]

| Major depressive disorder

| File:Vincent Van Gogh - Sorrow.JPG

|-

| male breast cancer

| class of disease

| breast cancer
male breast neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1614 DOID:1614]

|

|

|

|-

| male genital organ stricture

| class of disease

| male reproductive system disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12333 DOID:12333]

|

|

|

|-

| male genital organ vascular disease

| class of disease

| male reproductive system disease
vascular disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12335 DOID:12335]

|

|

|

|-

| male infertility

| class of disease
symptom or sign

| male reproductive system disease
infertility
sexual impotence
disease

| inability to father a child

| [http://www.disease-ontology.org/?id=DOID:12336 DOID:12336]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.365.700 C12.294.365.700]

| Male infertility

|

|-

| male reproductive organ benign neoplasm

| class of disease

| reproductive organ benign neoplasm
male reproductive system neoplasm
male reproductive system disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060087 DOID:0060087]

|

|

|

|-

| male reproductive organ cancer

| class of disease

| reproductive organ cancer
male reproductive system neoplasm
male reproductive system disease

| cancer that is manifested in the male genital system

| [http://www.disease-ontology.org/?id=DOID:3856 DOID:3856]

|

|

|

|-

| male reproductive system disease

| class of disease

| reproductive system disease
male urogenital disease

| reproductive system disease that affects male reproductive organs

| [http://www.disease-ontology.org/?id=DOID:48 DOID:48]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294 C12.294]

| Diseases and disorders of the male reproductive system

|

|-

| male urethral cancer

| class of disease

| urethral cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:736 DOID:736]

|

|

|

|-

| maleic anhydride allergic asthma

| class of disease

| allergic asthma
maleic anhydride exposure

| allergic asthma that has allergic trigger maleic anhydride

| [http://www.disease-ontology.org/?id=DOID:0040049 DOID:0040049]

|

|

|

|-

| malignant acrospiroma

| class of disease

| acrospiroma
sweat gland cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5570 DOID:5570]

|

| Malignant acrospiroma

|

|-

| malignant adenofibroma

| class of disease

| carcinosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4422 DOID:4422]

|

|

|

|-

| malignant adult ependymoma

| class of disease

| ependymal tumor
anaplastic ependymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5890 DOID:5890]

|

|

|

|-

| malignant anus melanoma

| class of disease

| anal cancer
mucosal melanoma
melanoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14145 DOID:14145]

|

|

|

|-

| malignant biphasic mesothelioma

| class of disease

| mesothelioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4486 DOID:4486]

|

|

|

|-

| malignant breast melanoma

| class of disease

| breast cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4364 DOID:4364]

|

|

|

|-

| malignant cardiac germ cell tumor

| class of disease

| heart cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14535 DOID:14535]

|

|

|

|-

| malignant cardiac peripheral nerve sheath neoplasm

| class of disease

| malignant peripheral nerve sheath tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14534 DOID:14534]

|

|

|

|-

| malignant childhood germ cell neoplasm

| class of disease

| pediatric germ cell tumor
germ cell cancer
childhood cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8149 DOID:8149]

|

|

|

|-

| malignant ciliary body melanoma

| class of disease

| ciliary body cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6524 DOID:6524]

|

|

|

|-

| malignant conjunctival melanoma

| class of disease

| conjunctival cancer
ocular melanoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1751 DOID:1751]

|

|

|

|-

| malignant cystadenoma

| class of disease

| adenocarcinoma
cystadenoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:60004 DOID:60004]

|

|

|

|-

| malignant cystic nephroma

| class of disease

| kidney cancer
nephroblastoma
childhood multilocular cystic kidney neoplasm
kidney cortex disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7571 DOID:7571]

|

|

|

|-

| malignant dermis tumor

| class of disease

| skin cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5274 DOID:5274]

|

|

|

|-

| malignant epithelial mesothelioma

| class of disease

| mesothelioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4489 DOID:4489]

|

|

|

|-

| malignant epithelioid hemangioendothelioma

| class of disease

| malignant hemangioma
epithelioid hemangioendothelioma

| A malignant hemangioma characterized by the presence of epithelioid endothelial cells. The neoplastic cells are arranged in cords and nests, which are embedded in a myxoid to hyalinized stroma.

| [http://www.disease-ontology.org/?id=DOID:0080190 DOID:0080190]

|

|

|

|-

| malignant essential hypertension

| class of disease

| essential hypertension

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10823 DOID:10823]

|

|

|

|-

| malignant eyelid melanoma

| class of disease

| skin melanoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10040 DOID:10040]

|

|

|

|-

| malignant fibrous histiocytoma

| class of disease

| histiocytoma
fibrous histiocytoma
sarcoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:1907 DOID:1907]

|

|

|

|-

| malignant fibrous histiocytoma of bone

| class of disease

| connective tissue neoplasm
osteosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3352 DOID:3352]

|

|

|

|-

| malignant gastric germ cell tumor

| class of disease

| stomach cancer
extragonadal germ cell cancer
gastrointestinal system disease
gastrointestinal system cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6949 DOID:6949]
[http://www.disease-ontology.org/?id=DOID:4716 DOID:4716]

|

|

|

|-

| malignant gastric granular cell tumor

| class of disease

| stomach cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10536 DOID:10536]

|

|

|

|-

| malignant gastric teratoma

| class of disease

| malignant gastric germ cell tumor
gastric teratoma
extragonadal non-dysgerminomatous germ cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6948 DOID:6948]

|

|

|

|-

| malignant giant cell tumor

| class of disease

| giant cell tumor
connective tissue neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2705 DOID:2705]

|

|

|

|-

| malignant giant cell tumor of soft parts

| class of disease

| malignant fibrous histiocytoma
malignant giant cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5638 DOID:5638]

|

|

|

|-

| malignant giant cell tumor of the tendon sheath

| class of disease

| synovium cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2704 DOID:2704]

|

|

|

|-

| malignant glandular tumor of peripheral nerve sheath

| class of disease

| malignant peripheral nerve sheath tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8420 DOID:8420]

|

|

|

|-

| malignant granular cell esophageal tumor

| class of disease

| esophageal cancer
granular cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5040 DOID:5040]

|

|

|

|-

| malignant granular cell myoblastoma

| class of disease

| skin cancer
malignant peripheral nerve neoplasm
granular cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5042 DOID:5042]

|

|

|

|-

| malignant granular cell skin tumor

| class of disease

| malignant dermis tumor
malignant granular cell myoblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7639 DOID:7639]

|

|

|

|-

| malignant hemangioma

| class of disease

| sarcoma
vascular cancer
malignant mixed tumor

| cell type cancer of vascular origin, characterized by proliferation of endothelial cells in and about the vascular lumen

| [http://www.disease-ontology.org/?id=DOID:0080189 DOID:0080189]

|

|

|

|-

| malignant hypertension

| class of disease
symptom or sign

| arterial hypertension
hypertensive crisis
disease

| condition of markedly elevated blood pressure with diastolic pressure typically greater than 120 mm Hg

| [http://www.disease-ontology.org/?id=DOID:10824 DOID:10824]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.489.330 C14.907.489.330]

|

|

|-

| malignant hypertensive renal disease

| class of disease

| renal hypertension

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10177 DOID:10177]

|

|

|

|-

| malignant leptomeningeal tumor

| class of disease

| meningioma
malignant neoplasm of meninges
meningeal carcinomatosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6086 DOID:6086]

|

|

|

|-

| malignant mediastinal neurogenic neoplasm

| class of disease

| mediastinal cancer

| mediastinal cancer that has material basis in neural cells

| [http://www.disease-ontology.org/?id=DOID:4691 DOID:4691]

|

|

|

|-

| malignant mediastinum hemangiopericytoma

| class of disease

| hemangiopericytoma
hemangiopericytoma, malignant
mediastinal cancer

| hemangiopericytoma and sarcoma of the mediastinum that is located in the mediastinum

| [http://www.disease-ontology.org/?id=DOID:6209 DOID:6209]

|

|

|

|-

| malignant melanocytic neoplasm of the peripheral nerve sheath

| class of disease

| malignant peripheral nerve sheath tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6345 DOID:6345]

|

|

|

|-

| malignant melanocytic peripheral nerve sheath tumor of mediastinum

| class of disease

| mediastinal cancer
peripheral neuropathy
malignant melanocytic neoplasm of the peripheral nerve sheath
mediastinum sarcoma
nervous system cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7077 DOID:7077]

|

|

|

|-

| malignant mesenchymoma

| class of disease

| mesenchymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5758 DOID:5758]

|

|

|

|-

| malignant mixed tumor

| class of disease

| Mixed tumor
cell type cancer

| cell type cancer that has material basis in cells from two tissues

| [http://www.disease-ontology.org/?id=DOID:154 DOID:154]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.435.525 C04.557.435.525]

|

|

|-

| malignant neoplasm of acoustic nerve

| class of disease

| cranial nerve malignant neoplasm
vestibulocochlear nerve neoplasm
inner ear cancer
vestibulocochlear nerve disease
ear neoplasms

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2814 DOID:2814]

|

|

|

|-

| malignant neoplasm of short bones of lower limb

| class of disease

| long bones of lower limb cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10151 DOID:10151]

|

|

|

|-

| malignant oculomotor nerve tumor

| class of disease

| cranial nerve III tumor
cranial nerve malignant neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2816 DOID:2816]

|

|

|

|-

| malignant otitis externa

| class of disease

| otitis externa
complications of diabetes mellitus

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10516 DOID:10516]

|

|

|

|-

| malignant ovarian Brenner tumor

| class of disease

| ovarian cancer
ovarian Brenner tumor
malignant ovarian surface epithelial-stromal neoplasm

| malignant ovarian surface epithelial-stromal neoplasm that has material basis in the surface epithelium of the ovary

| [http://www.disease-ontology.org/?id=DOID:4217 DOID:4217]

|

|

|

|-

| malignant ovarian cyst

| class of disease

| ovarian cancer
ovarian cyst

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2145 DOID:2145]

|

|

|

|-

| malignant ovarian germ cell neoplasm

| class of disease

| ovarian germ cell neoplasm
rare gynecological tumor
germ cell cancer
ovarian cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2155 DOID:2155]

|

|

|

|-

| malignant ovarian surface epithelial-stromal neoplasm

| class of disease

| surface epithelial-stromal tumor
ovarian cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2151 DOID:2151]

|

|

|

|-

| malignant parietal pleura tumor

| class of disease

| pleural cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14032 DOID:14032]

|

|

|

|-

| malignant pediatric adrenal gland pheochromocytoma

| class of disease

| adrenal gland pheochromocytoma

| adrenal gland pheochromocytoma that is characterized by rare chromaffin cell tumors which secrete catecholamines, and has a higher prevalence of hereditary factors and metastatis in children than adults

| [http://www.disease-ontology.org/?id=DOID:0070325 DOID:0070325]

|

|

|

|-

| malignant peripheral nerve sheath tumor

| class of disease

| nerve sheath neoplasms
malignant peripheral nerve neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5940 DOID:5940]

|

| Malignant peripheral nerve sheath tumor

|

|-

| malignant peritoneal solitary fibrous tumor

| class of disease

| peritoneum cancer
peritoneal solitary fibrous tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4490 DOID:4490]

|

|

|

|-

| malignant pheochromocytoma

| class of disease

| adrenal medulla cancer

| adrenal medulla cancer that arises within the adrenal medulla, releasing epinephrines and norepinephrines hormones

| [http://www.disease-ontology.org/?id=DOID:0080347 DOID:0080347]

|

|

|

|-

| malignant pineal area germ cell neoplasm

| class of disease

| pinealoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1660 DOID:1660]

|

|

|

|-

| malignant pleural mesothelioma

| class of disease

| pleural cancer
benign pleural mesothelioma
mesothelioma
squamous cell carcinoma
respiratory system cancer
pleural disease

| pleural cancer that has material basis in mesothelium cells

| [http://www.disease-ontology.org/?id=DOID:7474 DOID:7474]

|

| Pleural mesothelioma

|

|-

| malignant renovascular hypertension

| class of disease

| malignant secondary hypertension
renovascular hypertension
renal hypertension

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13730 DOID:13730]

|

|

|

|-

| malignant secondary hypertension

| class of disease

| secondary hypertension

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13731 DOID:13731]

|

|

|

|-

| malignant skin fibrous histiocytoma

| class of disease

| malignant dermis tumor
malignant fibrous histiocytoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1906 DOID:1906]

|

|

|

|-

| malignant spindle cell melanoma

| class of disease

| melanoma
hemangiopericytoma
spindle cell cancer

| melanoma that is most commonly located in sun-exposed skin and results in formation of spindle-like shaped cells that have a high recurrence rate even with treatment

| [http://www.disease-ontology.org/?id=DOID:3162 DOID:3162]

|

|

|

|-

| malignant spiradenoma

| class of disease

| eccrine sweat gland cancer
apocrine sweat gland cancer
spiradenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7960 DOID:7960]

|

|

|

|-

| malignant struma ovarii

| class of disease

| struma ovarii
immature teratoma of ovary

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5208 DOID:5208]

|

|

|

|-

| malignant syringoma

| class of disease

| eccrine sweat gland cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5569 DOID:5569]

|

|

|

|-

| malignant triton tumor

| class of disease

| malignant peripheral nerve sheath tumor

| human disease

| [http://www.disease-ontology.org/?id=DOID:6707 DOID:6707]

|

|

|

|-

| malignant tumor of undescended testis

| class of disease

| testicular cancer
cryptorchidism

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12276 DOID:12276]

|

|

|

|-

| malignant type A thymoma

| class of disease

| spindle cell thymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7927 DOID:7927]

|

|

|

|-

| malignant type AB thymoma

| class of disease

| mixed type thymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6723 DOID:6723]

|

|

|

|-

| malignant visceral pleura tumor

| class of disease

| pleural cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14033 DOID:14033]

|

|

|

|-

| malt worker's lung

| class of disease

| extrinsic allergic alveolitis

| extrinsic allergic alveolitis which is caused by inhalation of fungal spores of Aspergillus clavatus and Aspergillus fumigatus from moldy barley

| [http://www.disease-ontology.org/?id=DOID:2314 DOID:2314]

|

|

|

|-

| mammary Paget's disease

| class of disease

| breast adenocarcinoma
disease

| type of cancer that may have the appearance of eczema, involving the nipple

| [http://www.disease-ontology.org/?id=DOID:3443 DOID:3443]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.240.187.500 C04.557.470.200.240.187.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.615.275.625 C04.557.470.615.275.625]

| Paget's disease of the breast

|

|-

| mammary analogue secretory carcinoma

| class of disease

| salivary gland cancer
carcinoma
salivary gland carcinoma
secretory carcinoma

| salivary gland neoplasm

| [http://www.disease-ontology.org/?id=DOID:0080808 DOID:0080808]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.588 C04.557.470.200.588]

|

|

|-

| mammary myofibroblastoma

| class of disease

| benign neoplasm
muscle tissue neoplasm
breast benign neoplasm

| rare, benign tumor of the breast

| [http://www.disease-ontology.org/?id=DOID:1629 DOID:1629]

|

|

|

|-

| mantle cell lymphoma

| class of disease

| B-cell lymphoma
aggressive B-cell non-Hodgkin lymphoma
disease

| B-cell lymphocytic neoplasm due to CD5 positive antigen-naive pregerminal center B-cell within the mantle zone that surrounds normal germinal center follicles

| [http://www.disease-ontology.org/?id=DOID:0050746 DOID:0050746]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386.480.525 C04.557.386.480.525]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.569.480.525 C15.604.515.569.480.525]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.761.480.525 C20.683.515.761.480.525]

| Mantle cell lymphoma

| File:Mantle cell lymphoma - intermed mag.jpg

|-

| marasmus

| class of disease

| protein-energy malnutrition
disease

| form of severe malnutrition characterized by energy deficiency

| [http://www.disease-ontology.org/?id=DOID:12328 DOID:12328]

|

| Marasmus

| File:Starved child.jpg

|-

| marginal corneal ulcer

| class of disease

| corneal ulcer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10441 DOID:10441]

|

|

|

|-

| marginal zone B-cell lymphoma

| class of disease

| B-cell lymphoma
leukocyte disease

| group of lymphomas

| [http://www.disease-ontology.org/?id=DOID:0050748 DOID:0050748]

|

|

| File:Marginal zone lymphoma - kidney -- high mag.jpg

|-

| mast cell leukemia

| class of disease

| leukemia
rare bone disease
mastocytoma

| rare leukemia (blood cancer) involving mast cells

| [http://www.disease-ontology.org/?id=DOID:9254 DOID:9254]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.440 C04.557.337.440]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.539.275.440 C04.557.337.539.275.440]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.762.750.750.500 C20.762.750.750.500]

| Mast cell leukemia

|

|-

| mast cell sarcoma

| class of disease

| sarcoma
mastocytoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:355 DOID:355]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.465.124 C04.557.450.565.465.124]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.762.750.375 C20.762.750.375]

|

| File:Mast Cell Sarcoma.jpg

|-

| mastitis

| class of disease
symptom or sign

| breast disease
breastfeeding difficulties
inflammatory disease
reproductive system disease
skin and integumentary tissue symptom
disease

| inflammation of the breast

| [http://www.disease-ontology.org/?id=DOID:10690 DOID:10690]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.844.603 C13.703.844.603]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.090.968 C17.800.090.968]

| Mastitis

| File:Atlas of clinical surgery; with special reference to diagnosis and treatment for practitioners and students (1908) (14768289625).jpg

|-

| mastocytoma

| class of disease

| tumor of hematopoietic and lymphoid tissues
myeloid neoplasm

| solid tumor consisting of mast cells, generally benign

| [http://www.disease-ontology.org/?id=DOID:3664 DOID:3664]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.465.249 C04.557.450.565.465.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.762.750.469 C20.762.750.469]

| Mastocytoma

|

|-

| mastoiditis

| class of disease

| bone inflammation disease
middle ear disease
disease

| middle ear disease characterized by an inflammation of the mucosal lining of the mastoid antrum and the mastoid air cell system inside the mastoid process

| [http://www.disease-ontology.org/?id=DOID:0060322 DOID:0060322]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.539.160.495.500 C01.539.160.495.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.165.495.249 C05.116.165.495.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.218.705.663.652 C09.218.705.663.652]

| Mastoiditis

| File:Mastoiditis1.jpg

|-

| mature B-cell neoplasm

| class of disease

| B-cell lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:706 DOID:706]

|

|

|

|-

| mature T-cell and NK-cell lymphoma

| class of disease

| non-Hodgkin lymphoma
mature T-cell neoplasm

| non-Hodgkin lymphoma that has material basis in mature T lymphocytes and natural killer cells

| [http://www.disease-ontology.org/?id=DOID:0050743 DOID:0050743]

|

|

|

|-

| mature cataract

| class of disease

| senile cataract

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13717 DOID:13717]

|

|

|

|-

| mature gastric teratoma

| class of disease

| gastric teratoma
mature teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8118 DOID:8118]

|

|

|

|-

| mature teratoma

| class of disease

| teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5566 DOID:5566]

|

|

| File:Mature teratoma Case 164 (5462532633).jpg

|-

| mature teratoma of the ovary

| class of disease

| mature teratoma
ovarian biphasic or triphasic teratoma
ovarian germ cell teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6231 DOID:6231]

|

| Mature teratoma of ovary

|

|-

| maturity-onset diabetes of the young

| class of disease

| diabetes
autosomal dominant disease
disease

| genetic disease that has material basis in mutations in the MODY genes disrupting insulin production

| [http://www.disease-ontology.org/?id=DOID:0050524 DOID:0050524]

|

|

|

|-

| maturity-onset diabetes of the young type 14

| class of disease

| maturity-onset diabetes of the young

| maturity-onset diabetes of the young that has material basis in heterozygous mutation in the APPL1 gene on chromosome 3p14

| [http://www.disease-ontology.org/?id=DOID:0111111 DOID:0111111]

|

|

|

|-

| maturity-onset diabetes of the young type 2

| class of disease

| maturity-onset diabetes of the young

| maturity-onset diabetes of the young that has material basis in heterozygous mutation in the GCK gene on chromosome 7p13

| [http://www.disease-ontology.org/?id=DOID:0111100 DOID:0111100]

|

|

|

|-

| maturity-onset diabetes of the young type 3

| class of disease

| maturity-onset diabetes of the young

| A maturity-onset diabetes of the young that has material basis in mutation in the HNF1A gene on chromosome 12q24.31.

| [http://www.disease-ontology.org/?id=DOID:0111102 DOID:0111102]

|

|

|

|-

| maturity-onset diabetes of the young type 4

| class of disease

| maturity-onset diabetes of the young

| A maturity-onset diabetes of the young that has material basis in mutation in the PDX1 gene on chromosome 13q12.2.

| [http://www.disease-ontology.org/?id=DOID:0111103 DOID:0111103]

|

|

|

|-

| maturity-onset diabetes of the young type 5

| class of disease

| maturity-onset diabetes of the young

| maturity-onset diabetes of the young characterized by abnormal renal development resuting in non-diabetic kidney disease and diabetes that has material basis in mutation in the HNF1B gene on chromosome 17q12

| [http://www.disease-ontology.org/?id=DOID:0111101 DOID:0111101]

|

|

|

|-

| maturity-onset diabetes of the young type 6

| class of disease

| maturity-onset diabetes of the young

| maturity-onset diabetes of the young that has material basis in heterozygous mutation in the NEUROD1 gene on chromosome 2q31

| [http://www.disease-ontology.org/?id=DOID:0111104 DOID:0111104]

|

|

|

|-

| maxillary sinus cancer

| class of disease

| paranasal sinus cancer
maxillary sinus neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1357 DOID:1357]

|

|

|

|-

| maxillary sinus cholesteatoma

| class of disease

| paranasal sinus disease
cholesteatoma
mouth disease

| cholesteatoma located in paranasal sinus

| [http://www.disease-ontology.org/?id=DOID:867 DOID:867]

|

|

|

|-

| maxillary sinusitis

| class of disease

| nose disease
sinusitis
mouth disease

| sinusitis which involves infection of maxillary sinuses that causes pain or pressure over the cheeks just below the eyes, tooth ache, and headache

| [http://www.disease-ontology.org/?id=DOID:2051 DOID:2051]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.460.692.752.578 C08.460.692.752.578]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.730.749.578 C08.730.749.578]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.603.692.752.578 C09.603.692.752.578]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.748.749.578 C01.748.749.578]

|

|

|-

| mechanical ectropion

| class of disease

| ectropion

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1569 DOID:1569]

|

|

|

|-

| mechanical entropion

| class of disease

| entropion

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13112 DOID:13112]

|

|

|

|-

| mechanical lagophthalmos

| class of disease

| lagophthalmos

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13037 DOID:13037]

|

|

|

|-

| mechanical strabismus

| class of disease

| strabismus

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9306 DOID:9306]

|

|

|

|-

| meconium aspiration syndrome

| class of disease

| lung disease
perinatal respiratory disorder
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11049 DOID:11049]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.520.687 C08.381.520.687]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.618.580 C08.618.580]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.277.785 C13.703.277.785]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.300.580 C16.300.580]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.614.580 C16.614.580]

| Meconium aspiration syndrome

| File:Amniotic fluid and meconium aspiration Case 179 (5613700230).jpg

|-

| medial epicondylitis

| class of disease

| bone inflammation disease
arm injuries
disease

| bone inflammation disease that results in inflammation located in epicondyle

| [http://www.disease-ontology.org/?id=DOID:14087 DOID:14087]

|

| Golfer's elbow

| File:Golfers-Elbow SAG.jpg

|-

| median arcuate ligament syndrome

| class of disease

| vascular surgery
rare abdominal surgical disease
syndrome

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9892 DOID:9892]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.198.929C14.240.850.922 C06.198.929C14.240.850.922]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.137.527 C14.907.137.527]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.240.850.898 C16.131.240.850.898]

| Median arcuate ligament syndrome

|

|-

| median nerve neuropathy

| class of disease

| mononeuritis of upper limb and mononeuritis multiplex
brachial plexus neuritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:571 DOID:571]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.500.500 C10.668.829.500.500]

|

|

|-

| mediastinal cancer

| class of disease

| thoracic cancer
mediastinal neoplasm

| thoracic cancer that is located in the mediastinum

| [http://www.disease-ontology.org/?id=DOID:5559 DOID:5559]

|

| Mediastinal cancers

|

|-

| mediastinal granular cell myoblastoma

| class of disease

| malignant mediastinal neurogenic neoplasm
granular cell tumor
mediastinal neurilemmoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5046 DOID:5046]

|

|

|

|-

| mediastinal gray zone lymphoma

| class of disease

| gray zone lymphoma
mediastinal malignant lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6867 DOID:6867]

|

|

|

|-

| mediastinal lipomatosis

| class of disease

| lipomatosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3926 DOID:3926]

|

|

| File:MediastinalLipomatosisCT.png

|-

| mediastinal malignant lymphoma

| class of disease

| mediastinal cancer
lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6868 DOID:6868]

|

|

|

|-

| mediastinal melanocytic neurilemmoma

| class of disease

| melanotic neurilemmoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6484 DOID:6484]

|

|

|

|-

| mediastinal mesenchymal tumor

| class of disease

| mediastinal neoplasm
mesenchymal cell neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5560 DOID:5560]

|

|

|

|-

| mediastinal neurilemmoma

| class of disease

| peripheral nerve schwannoma
mediastinal neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6175 DOID:6175]

|

|

|

|-

| mediastinal osteogenic sarcoma

| class of disease

| extraosseous osteosarcoma
mediastinum sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6208 DOID:6208]

|

|

|

|-

| mediastinitis

| class of disease

| connective tissue disease
mediastinal disease
inflammatory disease
disease

| inflammatory process affecting the mediastinum

| [http://www.disease-ontology.org/?id=DOID:819 DOID:819]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.846.187.790 C08.846.187.790]

|

|

|-

| mediastinum angiosarcoma

| class of disease

| angiosarcoma
mediastinum sarcoma

| angiosarcoma and sarcoma of the mediastinum that is located in the mediastinum

| [http://www.disease-ontology.org/?id=DOID:4525 DOID:4525]

|

|

|

|-

| mediastinum leiomyoma

| class of disease

| leiomyoma
benign neoplasm of mediastinum
thoracic benign neoplasm
mediastinal neurilemmoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5123 DOID:5123]

|

|

|

|-

| mediastinum leiomyosarcoma

| class of disease

| mediastinum sarcoma
leiomyosarcoma

| leiomyosarcoma and sarcoma of the mediastinum that derive from smooth muscle and are usually located in the esophagus or located in the main vessels

| [http://www.disease-ontology.org/?id=DOID:5292 DOID:5292]

|

|

|

|-

| mediastinum liposarcoma

| class of disease

| liposarcoma
mediastinum sarcoma

| liposarcoma and mediastinum sarcoma that is located in the mediastinum

| [http://www.disease-ontology.org/?id=DOID:5713 DOID:5713]

|

|

|

|-

| mediastinum neurofibroma

| class of disease

| malignant mediastinal neurogenic neoplasm
neurofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12064 DOID:12064]

|

|

|

|-

| mediastinum rhabdomyosarcoma

| class of disease

| mediastinum sarcoma
rhabdomyosarcoma

| rhabdomyosarcoma and sarcoma of the mediastinum that is located in the mediastinum and affects children and adolescents

| [http://www.disease-ontology.org/?id=DOID:4049 DOID:4049]

|

|

|

|-

| mediastinum sarcoma

| class of disease

| mediastinal cancer
sarcoma
mediastinal soft tissue cancer

| sarcoma and malignant mediastinal mesenchymnal tumor that is located in the mediastinum

| [http://www.disease-ontology.org/?id=DOID:4050 DOID:4050]

|

|

|

|-

| mediastinum seminoma

| class of disease

| mediastinal cancer
extragonadal seminoma
mediastinal malignant germ cell tumor
germ cell cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6249 DOID:6249]

|

|

|

|-

| mediastinum synovial sarcoma

| class of disease

| mediastinum sarcoma
synovial sarcoma

| sarcoma of the mediastinum and synovial sarcoma that is located in the mediastinum

| [http://www.disease-ontology.org/?id=DOID:5488 DOID:5488]

|

|

|

|-

| mediastinum teratoma

| class of disease

| mediastinal cancer
mediastinal germ cell tumor
teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5568 DOID:5568]

|

|

|

|-

| medullary colon carcinoma

| class of disease

| colon carcinoma

| colon carcinoma that is characterized by a solid growth pattern

| [http://www.disease-ontology.org/?id=DOID:0080183 DOID:0080183]

|

|

|

|-

| medulloadrenal hyperfunction

| class of disease

| adrenal gland disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12257 DOID:12257]

|

|

|

|-

| medulloblastoma SHH activated

| class of disease

| medulloblastoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080703 DOID:0080703]

|

|

|

|-

| medulloblastoma SHH activated and TP53 mutant

| class of disease

| medulloblastoma SHH activated

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080704 DOID:0080704]

|

|

|

|-

| medulloblastoma SHH activated and TP53 wild-type

| class of disease

| medulloblastoma SHH activated

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080705 DOID:0080705]

|

|

|

|-

| medulloblastoma WNT activated

| class of disease

| medulloblastoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080702 DOID:0080702]

|

|

|

|-

| medulloblastoma non-WNT/non-SHH

| class of disease

| medulloblastoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080706 DOID:0080706]

|

|

|

|-

| medulloblastoma non-WNT/non-SHH group 3

| class of disease

| medulloblastoma non-WNT/non-SHH

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080707 DOID:0080707]

|

|

|

|-

| medulloblastoma non-WNT/non-SHH group 4

| class of disease

| medulloblastoma non-WNT/non-SHH

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080708 DOID:0080708]

|

|

|

|-

| medulloepithelioma

| class of disease

| central nervous system primitive neuroectodermal neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4790 DOID:4790]

|

| Medulloepithelioma

|

|-

| medullomyoblastoma

| class of disease

| medulloblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3861 DOID:3861]

|

|

|

|-

| mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations

| class of disease

| syndromic intellectual disability
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111403 DOID:0111403]

|

|

|

|-

| megacolon

| class of disease

| colonic disease
disease

| colonic disease that is characterized by an abnormal dilation of the colon

| [http://www.disease-ontology.org/?id=DOID:11372 DOID:11372]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.158.701 C06.405.469.158.701]

| Megacolon

|

|-

| megaesophagus

| class of disease

| esophageal disease
disease

| abnormal dilation of the esophagus not due to obstruction

| [http://www.disease-ontology.org/?id=DOID:13186 DOID:13186]

|

|

|

|-

| megalencephalic leukoencephalopathy with subcortical cysts 1

| class of disease

| megalencephalic leukoencephalopathy with subcortical cysts
genetic disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080316 DOID:0080316]

|

|

|

|-

| meibomian cyst

| class of disease
symptom or sign

| internal hordeolum
blepharitis
disease

| Cyst in the eyelid caused by chronic granulomatous inflammation of Meibomian gland

| [http://www.disease-ontology.org/?id=DOID:9903 DOID:9903]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.182.197 C04.182.197]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.338.300 C11.338.300]

| Chalazion

| File:Chalazion.JPG

|-

| melancholia

| class of disease
symptom or sign

| major depressive disorder
mental depression
disease

| DSM-IV subtype of clinical depression

| [http://www.disease-ontology.org/?id=DOID:2848 DOID:2848]

|

|

| File:Accademia - La Meditazione by Domenico Fetti 1618.jpg

|-

| melanoacanthoma

| class of disease

| seborrheic keratosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11684 DOID:11684]

|

|

|

|-

| melanocytic psammomatous MPNST

| class of disease

| malignant melanocytic neoplasm of the peripheral nerve sheath

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6344 DOID:6344]

|

|

|

|-

| melanoma and neural system tumor syndrome

| class of disease

| hereditary neoplastic syndromes
rare nervous system tumor
rare genetic developmental defect during embryogenesis
inherited nervous system cancer-predisposing syndrome
nervous system cancer
genetic nervous system disorder
inherited tumor
autosomal dominant disease
syndrome

| Melanoma and neural system tumor syndrome is an extremely rare tumor association characterized by dual predisposition to melanoma and neural system tumors (typically astrocytoma; see this term)

| [http://www.disease-ontology.org/?id=DOID:0111511 DOID:0111511]

|

|

|

|-

| melanoma in congenital melanocytic nevus

| class of disease

| skin melanoma
congenital melanocytic nevus

| skin melanoma that arises from a congenital melanocytic nevus

| [http://www.disease-ontology.org/?id=DOID:0070327 DOID:0070327]

|

|

|

|-

| melanoma with features of a Spitz nevus

| class of disease

| Spitzoid lesion
melanoma
skin melanoma

| skin melanoma that is characterized by asymmetric shape, diameter greater than 1 cm, a lesion with a deep invasive component, and a high degree of cytologic atypia

| [http://www.disease-ontology.org/?id=DOID:0070326 DOID:0070326]

|

| Spitzoid melanoma

|

|-

| melanomatosis

| class of disease

| melanoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7206 DOID:7206]

|

|

|

|-

| melanotic medulloblastoma

| class of disease

| medulloblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3868 DOID:3868]

|

|

|

|-

| melanotic neurilemmoma

| class of disease

| neurilemmoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3205 DOID:3205]

|

|

|

|-

| melanotic neuroectodermal tumor

| class of disease

| bone benign neoplasm
neuroectodermal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:166 DOID:166]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.630 C04.557.465.625.630]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.630 C04.557.580.625.630]

| Melanotic neuroectodermal tumor of infancy

| File:Oral melanotic neuroectodermal tumor infancy LDRT 369 08.tif

|-

| melon allergy

| class of disease

| fruit allergy

| fruit allergy triggered by Cucumis melo plant fruit food product.

| [http://www.disease-ontology.org/?id=DOID:0060509 DOID:0060509]

|

|

|

|-

| melphalan allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger melphalan

| [http://www.disease-ontology.org/?id=DOID:0040066 DOID:0040066]

|

|

|

|-

| membranous glomerulonephritis

| class of disease

| glomerulonephritis
lupus nephritis
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:10976 DOID:10976]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.419.570.363.625 C12.777.419.570.363.625]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.419.570.363.625 C13.351.968.419.570.363.625]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.535 C20.111.535]

| Membranous glomerulonephritis

|

|-

| meningeal melanocytoma

| class of disease

| central nervous system melanocytic neoplasm
primary melanocytic tumor of central nervous system
malignant neoplasm of meninges

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5900 DOID:5900]

|

|

|

|-

| meningeal melanoma

| class of disease

| malignant leptomeningeal tumor
central nervous system melanocytic neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6085 DOID:6085]

|

|

|

|-

| meningeal melanomatosis

| class of disease

| central nervous system melanocytic neoplasm
melanomatosis
malignant neoplasm of meninges

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8243 DOID:8243]

|

|

|

|-

| meninges hemangiopericytoma

| class of disease

| meningioma
hemangiopericytoma
malignant neoplasm of meninges

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4957 DOID:4957]

|

|

|

|-

| meninges sarcoma

| class of disease

| meningioma
malignant neoplasm of meninges
sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7614 DOID:7614]

|

|

|

|-

| meningioma

| class of disease

| meningeal neoplasm
central nervous system cancer
disease

| Tumor forms from meninges

| [http://www.disease-ontology.org/?id=DOID:3565 DOID:3565]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.520 C04.557.580.520]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.645.520 C04.557.645.520]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.614.250.580.500 C04.588.614.250.580.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.551.240.500.500 C10.551.240.500.500]

| Meningioma

| File:Contrast enhanced meningioma.jpg

|-

| meningitis

| class of disease
symptom or sign

| encephalomyelitis
central nervous system disease
disease

| inflammation of the membranes around the brain and spinal cord

| [http://www.disease-ontology.org/?id=DOID:9471 DOID:9471]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.614 C10.228.614]

| Meningitis

| File:Meninges-en.svg

|-

| meningocele

| class of disease

| spina bifida
cephalocele

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1088 DOID:1088]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.500.680.598 C10.500.680.598]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.666.680.598 C16.131.666.680.598]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.300.707.968 C23.300.707.968]

|

|

|-

| meningococcal meningitis

| class of disease

| bacterial meningitis
meningococcal disease

| bacterial meningitis that has material basis in Neisseria meningitidis infection

| [http://www.disease-ontology.org/?id=DOID:0080176 DOID:0080176]
[http://www.disease-ontology.org/?id=DOID:9929 DOID:9929]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.223.500.750 C01.150.252.223.500.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.400.625.549.449 C01.150.252.400.625.549.449]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.228.180.500.750 C10.228.228.180.500.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.586.625.280.505 C10.586.625.280.505]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.207.180.500.750 C01.207.180.500.750]

|

|

|-

| meningoencephalitis

| class of disease
symptom or sign

| central nervous system disease
meningitis
encephalitis
neurological symptom
disease

| central nervous system disease that involves encephalitis which occurs along with meningitis

| [http://www.disease-ontology.org/?id=DOID:10554 DOID:10554]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.430.550 C10.228.140.430.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.228.245.550 C10.228.228.245.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.228.570 C10.228.228.570]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.207.245.550 C01.207.245.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.207.570 C01.207.570]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.586.250.550 C10.586.250.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.586.625.500 C10.586.625.500]

|

| File:Méningo-encéphalite amibienne primitive.JPG

|-

| meningothelial meningioma

| class of disease

| meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7212 DOID:7212]

|

|

|

|-

| meningovascular neurosyphilis

| class of disease

| tertiary neurosyphilis
syphilitic meningitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050491 DOID:0050491]

|

|

|

|-

| mental depression

| class of disease
symptom or sign

| mood disorder
neurological and physiological symptom
disease

| state of low mood and aversion to activity, which can affect a person's thoughts, behavior, motivation, feelings, and sense of well-being

| [http://www.disease-ontology.org/?id=DOID:1596 DOID:1596]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F01.145.126.350 F01.145.126.350]

| Depression (mood)

| File:Depression-loss of loved one.jpg

|-

| mental disorder

| class of disease

| disease

| distressing thought or behavior pattern

| [http://www.disease-ontology.org/?id=DOID:150 DOID:150]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03 F03]

| Mental and behavioural diseases and disorders

| File:Gautier - Salpetriere.JPG

|-

| mepivacaine allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger mepivacaine

| [http://www.disease-ontology.org/?id=DOID:0040010 DOID:0040010]

|

|

|

|-

| meropenem allergy

| class of disease

| beta-lactam allergy
allergic asthma

| beta-lactam allergy that has allergic trigger meropenem

| [http://www.disease-ontology.org/?id=DOID:0040038 DOID:0040038]

|

|

|

|-

| mesangial proliferative glomerulonephritis

| class of disease

| glomerulonephritis
proliferative glomerulonephritis
lupus nephritis

| glomerulonephritis associated primarily with the mesangium

| [http://www.disease-ontology.org/?id=DOID:4783 DOID:4783]

|

|

|

|-

| mesenchymal cell neoplasm

| class of disease

| cell type cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3350 DOID:3350]

|

|

|

|-

| mesenchymal chondrosarcoma

| class of disease

| chondrosarcoma
mesenchymal cell neoplasm
small cell sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4545 DOID:4545]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.280.280 C04.557.450.565.280.280]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.300.280 C04.557.450.795.300.280]

|

|

|-

| mesenchymoma

| class of disease

| connective tissue neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2668 DOID:2668]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.435.500 C04.557.435.500]

|

|

|-

| mesenteric adenitis

| class of disease

| lymphadenitis
adenitis

| lymphadenitis

| [http://www.disease-ontology.org/?id=DOID:10782 DOID:10782]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.844.520 C06.844.520]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.315.618 C15.604.315.618]

| Mesenteric adenitis

|

|-

| mesenteric vascular occlusion

| class of disease

| peripheral vascular disease
mesenteric ischemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13252 DOID:13252]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.675 C06.405.469.675]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.844.550 C06.844.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.137.534 C14.907.137.534]

|

|

|-

| mesocestoidiasis

| class of disease

| parasitic helminthiasis infectious disease

| parasitic helminthiasis infectious disease that involves parasitic cestode infection caused by Mesocestoides lineatus resulting in nausea, diarrhea, abdominal discomfort and vomiting

| [http://www.disease-ontology.org/?id=DOID:0050253 DOID:0050253]

|

|

|

|-

| metabolic acidosis

| class of disease

| acidosis
acquired metabolic disease
disease

| lactic acidosis that has material basis in high levels of acid

| [http://www.disease-ontology.org/?id=DOID:0050758 DOID:0050758]

|

| Metabolic acidosis

|

|-

| metabolic disease

| class of disease

| disease
nutritional and metabolic diseases

| disease that involving errors in metabolic processes of building or degradation of molecules

| [http://www.disease-ontology.org/?id=DOID:0014667 DOID:0014667]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452 C18.452]

| Metabolic diseases and disorders

| File:Ragged red fibres - gtc - very high mag.jpg

|-

| metachronous kidney Wilms' tumor

| class of disease

| nephroblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5178 DOID:5178]

|

|

|

|-

| metachronous osteosarcoma of the bone

| class of disease

| osteosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3379 DOID:3379]

|

|

|

|-

| metal allergy

| class of disease

| allergy

| hypersensitivity reaction type I disease triggered by a metal

| [http://www.disease-ontology.org/?id=DOID:0060501 DOID:0060501]

|

| Metal allergies

|

|-

| metal metabolism disorder

| class of disease

| mineral metabolism disease
inherited metabolic disorder

| inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals

| [http://www.disease-ontology.org/?id=DOID:896 DOID:896]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.618 C16.320.565.618]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.618 C18.452.648.618]

|

|

|-

| metanephric adenoma

| class of disease

| renal adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6404 DOID:6404]

|

| Metanephric adenoma

|

|-

| metaphyseal dysplasia

| class of disease

| osteochondrodysplasia

| osteochondrodysplasia that results in thinning and the tendency to fracture located in bone

| [http://www.disease-ontology.org/?id=DOID:0080019 DOID:0080019]

|

|

|

|-

| metatypical basal cell carcinoma

| class of disease

| basal-cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4281 DOID:4281]

|

|

|

|-

| methemoglobinemia

| class of disease

| hemoglobinopathy
disease

| a form of toxic anemia characterized by the presence of methemoglobin in the blood

| [http://www.disease-ontology.org/?id=DOID:10783 DOID:10783]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.619 C15.378.619]

| Methemoglobinemia

|

|-

| methotrexate-associated lymphoproliferation

| class of disease

| lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5821 DOID:5821]

|

|

|

|-

| methyl isocyanate allergic asthma

| class of disease

| isocyanates allergic asthma

| allergic asthma to isocyanates that has allergic trigger methyl isocyanate

| [http://www.disease-ontology.org/?id=DOID:0040044 DOID:0040044]

|

|

|

|-

| methylmalonic acidemia cblB type

| class of disease

| methylmalonic acidemia
genetic disease
vitamin B12-responsive methylmalonic acidemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060743 DOID:0060743]

|

|

|

|-

| methylmalonic aciduria and homocystinuria type cblE

| class of disease

| methylmalonic acidemia
methylmalonic acidemia with homocystinuria

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050732 DOID:0050732]

|

|

|

|-

| methylmalonic aciduria and homocystinuria type cblG

| class of disease

| methylmalonic acidemia
methylmalonic acidemia with homocystinuria

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050733 DOID:0050733]

|

|

|

|-

| microcystic adenoma

| class of disease

| pancreatic cystadenoma
benign neoplasms by histologic type

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5403 DOID:5403]

|

|

|

|-

| microcystic meningioma

| class of disease

| meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4594 DOID:4594]

|

|

|

|-

| microcystic variant infiltrating bladder urothelial carcinoma

| class of disease

| invasive bladder transitional cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7971 DOID:7971]

|

|

|

|-

| microglandular adenosis

| class of disease

| breast disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5998 DOID:5998]

|

|

|

|-

| microglandular adenosis of breast

| class of disease

| microglandular adenosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8335 DOID:8335]

|

|

|

|-

| microinvasive cervical squamous cell carcinoma

| class of disease

| cervical squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8409 DOID:8409]

|

|

|

|-

| microinvasive gastric cancer

| class of disease

| gastric adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10541 DOID:10541]

|

|

|

|-

| microlissencephaly

| class of disease

| lissencephaly

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112234 DOID:0112234]

|

|

|

|-

| micronodular basal cell carcinoma

| class of disease

| basal-cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4289 DOID:4289]

|

|

|

|-

| microorchidism

| class of disease

| testicular disease
hypogonadism, male

| congenital human disease

| [http://www.disease-ontology.org/?id=DOID:11994 DOID:11994]

|

| Microorchidism

| File:Mikroorchie.jpg

|-

| micropapillary variant infiltrating bladder urothelial carcinoma

| class of disease

| invasive bladder transitional cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6976 DOID:6976]

|

|

|

|-

| micropapillomatosis labialis

| class of disease

| vulvar squamous papilloma
Vestibular papillomatosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6569 DOID:6569]

|

|

|

|-

| microphthalmia with brain and digit anomalies

| class of disease

| syndromic microphthalmia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111805 DOID:0111805]

|

|

|

|-

| microphthalmia–dermal aplasia–sclerocornea syndrome

| class of disease

| syndromic microphthalmia
syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111875 DOID:0111875]

|

|

|

|-

| microscopic breast papilloma

| class of disease

| breast duct papilloma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8225 DOID:8225]

|

|

|

|-

| microscopic colitis

| class of disease

| colitis
disease

| colitis that can only be diagnosed by the examination of colon tissue under a microscope

| [http://www.disease-ontology.org/?id=DOID:0060182 DOID:0060182]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.265.173 C06.405.205.265.173]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.158.188.173 C06.405.469.158.188.173]

| Microscopic colitis

|

|-

| middle cerebral artery infarction

| class of disease

| cerebral arterial disease
cerebral infarction
cerebral artery occlusion

| human disease

| [http://www.disease-ontology.org/?id=DOID:3525 DOID:3525]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.150.477.200.450 C10.228.140.300.150.477.200.450]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.510.200.387 C10.228.140.300.510.200.387]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.300.775.200.200.450 C10.228.140.300.775.200.200.450]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.092.477.200.450 C14.907.253.092.477.200.450]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.560.200.387 C14.907.253.560.200.387]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.253.855.200.200.450 C14.907.253.855.200.200.450]

|

|

|-

| middle ear adenoma

| class of disease

| sensory organ benign neoplasm
middle ear disease
neoplasm of middle ear
benign neoplasms by histologic type
benign neoplasm of ear

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5387 DOID:5387]

|

|

|

|-

| middle ear cancer

| class of disease

| neoplasm of middle ear
auricular cancer
middle ear disease

| auditory system cancer that is located in the middle ear

| [http://www.disease-ontology.org/?id=DOID:5099 DOID:5099]

|

|

|

|-

| middle ear cholesterol granuloma

| class of disease

| otitis media
cholesteatoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10852 DOID:10852]

|

|

|

|-

| middle lobe syndrome

| class of disease

| lung disease
atelectasis

| human disease

| [http://www.disease-ontology.org/?id=DOID:2810 DOID:2810]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.730.542 C08.381.730.542]

|

|

|-

| midface dysplasia

| class of disease

| osteochondrodysplasia
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050767 DOID:0050767]

|

|

|

|-

| midline cystocele

| class of disease

| pelvic organ prolapse
cystocele

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14131 DOID:14131]

|

|

|

|-

| migraine

| class of disease

| encephalopathy
disease

| disorder resulting in recurrent moderate-severe headaches

| [http://www.disease-ontology.org/?id=DOID:6364 DOID:6364]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.546.399.750 C10.228.140.546.399.750]

| Migraine

| File:Migraine.jpg

|-

| migraine with aura

| class of disease

| migraine

| migraine characterized by migraine headache which is preceded or accompanied by a transient focal neurological phenomenon

| [http://www.disease-ontology.org/?id=DOID:10024 DOID:10024]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.546.399.750.250 C10.228.140.546.399.750.250]

|

|

|-

| migraine without aura

| class of disease

| migraine
rare genetic headache disorder

| migraine that is characterized by migraine headaches that are not accompanied by an aura

| [http://www.disease-ontology.org/?id=DOID:12783 DOID:12783]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.546.399.750.450 C10.228.140.546.399.750.450]

|

|

|-

| mild pre-eclampsia

| class of disease

| pre-eclampsia

| pre-eclampsia characterized by the presence of hypertension without evidence of end-organ damage, in a woman who was normotensive before 20 weeks' gestation

| [http://www.disease-ontology.org/?id=DOID:10590 DOID:10590]

|

|

|

|-

| miliaria

| class of disease

| sweat gland disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1382 DOID:1382]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.946.492 C17.800.946.492]

| Miliaria (disease)

|

|-

| miliaria profunda

| class of disease

| miliaria

| miliaria that is characterized by ductal occlusion of the papillary dermis causing the gland's secretions to leak between the superficial and deep layers of the skin resulting in a rapidly-spreading flesh-colored rash

| [http://www.disease-ontology.org/?id=DOID:0070320 DOID:0070320]

|

|

|

|-

| miliaria pustulosa

| class of disease

| miliaria

| miliaria that is characterized by pustules resulting from inflammation and bacterial infection

| [http://www.disease-ontology.org/?id=DOID:0070319 DOID:0070319]

|

|

|

|-

| miliaria rubra

| class of disease

| miliaria

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11153 DOID:11153]

|

| Miliaria rubra

|

|-

| milk allergy

| class of disease

| food allergy
disease

| type of food allergy caused by milk

| [http://www.disease-ontology.org/?id=DOID:4376 DOID:4376]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.370.500 C20.543.480.370.500]

| Milk allergy

| File:Koemelkallegie-Eczeem in knieholte.jpg

|-

| mineral metabolism disease

| class of disease

| acquired metabolic disease
disorder of metabolite absorption and transport

| acquired metabolic disease that is characterized by abnormal mineral metabolism

| [http://www.disease-ontology.org/?id=DOID:0050032 DOID:0050032]

|

| Disorders of mineral metabolism

|

|-

| minor vestibular glands adenoma

| class of disease

| vestibular gland benign neoplasm
adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2075 DOID:2075]

|

|

|

|-

| mirror agnosia

| class of disease

| agnosia
visual agnosia

| agnosia that is a loss of the ability to acknowledge objects in the neglected field that are visible when a mirror reflects the object visible in the non-neglected field

| [http://www.disease-ontology.org/?id=DOID:0060144 DOID:0060144]

|

|

|

|-

| mirror movement disorder

| class of disease

| synkinesis
movement disorders

| movement disease characterized by involuntary movements of one side of the body that mirror intentional movements on the opposite side primarily involving the upper limbs

| [http://www.disease-ontology.org/?id=DOID:0111153 DOID:0111153]

|

|

|

|-

| mitochondrial DNA depletion syndrome 12b

| class of disease

| autosomal recessive disease
mitochondrial DNA depletion syndrome
mitochondrial DNA depletion syndrome 12

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080335 DOID:0080335]

|

|

|

|-

| mitochondrial DNA depletion syndrome 14

| class of disease

| mitochondrial DNA depletion syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080336 DOID:0080336]

|

|

|

|-

| mitochondrial DNA depletion syndrome 15

| class of disease

| autosomal recessive disease
mitochondrial DNA depletion syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080337 DOID:0080337]

|

|

|

|-

| mitochondrial DNA depletion syndrome 17

| class of disease

| mitochondrial DNA depletion syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070448 DOID:0070448]

|

|

|

|-

| mitochondrial DNA depletion syndrome 8b

| class of disease

| mitochondrial DNA depletion syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070331 DOID:0070331]

|

|

|

|-

| mitochondrial complex III deficiency

| class of disease

| mitochondrial disease

| mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial respiratory chain complex III

| [http://www.disease-ontology.org/?id=DOID:0111139 DOID:0111139]

|

|

|

|-

| mitochondrial complex V (ATP synthase) deficiency

| class of disease

| mitochondrial disease
mitochondrial complex deficiency

| mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial proton-transporting ATP synthase complex

| [http://www.disease-ontology.org/?id=DOID:0111143 DOID:0111143]

|

|

|

|-

| mitochondrial complex V (ATP synthase) deficiency mitochondrial type 1

| class of disease

| mitochondrial complex V (ATP synthase) deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111748 DOID:0111748]

|

|

|

|-

| mitochondrial complex V (ATP synthase) deficiency nuclear type 6

| class of disease

| mitochondrial complex V (ATP synthase) deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111749 DOID:0111749]

|

|

|

|-

| mitochondrial nonsyndromic sensorineural deafness

| class of disease

| sensorineural hearing loss
mitochondrial deafness

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111751 DOID:0111751]

|

|

|

|-

| mitochondrial type mitochondrial complex I deficiency

| class of disease

| mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112100 DOID:0112100]

|

|

|

|-

| mitochondrial type mitochondrial complex I deficiency 1

| class of disease

| mitochondrial type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112101 DOID:0112101]

|

|

|

|-

| mitral valve disease

| class of disease

| heart valve disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:61 DOID:61]

|

| Mitral valve diseases

|

|-

| mitral valve insufficiency

| class of disease

| mitral valve disease
valve insufficiency
disease

| disorder of the heart in which the mitral valve does not close properly when the heart pumps out blood

| [http://www.disease-ontology.org/?id=DOID:11502 DOID:11502]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.484.461 C14.280.484.461]

| Mitral valve insufficiency

|

|-

| mitral valve stenosis

| class of disease

| mitral valve disease
heart valve stenosis
disease

| mitral valve disease that is characterized by the narrowing of the orifice of the mitral valve of the heart

| [http://www.disease-ontology.org/?id=DOID:1754 DOID:1754]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.484.517 C14.280.484.517]

| Mitral valve stenosis

|

|-

| mixed astrocytoma-ependymoma

| class of disease

| mixed glioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7907 DOID:7907]

|

|

|

|-

| mixed astrocytoma-ependymoma-oligodendroglioma

| class of disease

| mixed glioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7817 DOID:7817]

|

|

|

|-

| mixed cell adenoma

| class of disease

| adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5385 DOID:5385]

|

|

|

|-

| mixed cell type adenoma of parathyroid

| class of disease

| parathyroid adenoma
mixed cell adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7610 DOID:7610]

|

|

|

|-

| mixed cell type kidney Wilms' tumor

| class of disease

| nephroblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5179 DOID:5179]

|

|

|

|-

| mixed cerebral palsy

| class of disease

| cerebral palsy

| subtype of cerebral palsy characterized by both the tight muscle tone of spastic cerebral palsy and the writhing, involuntary muscle movements of athetoid cerebral palsy

| [http://www.disease-ontology.org/?id=DOID:0050673 DOID:0050673]

|

|

|

|-

| mixed ductal-endocrine carcinoma

| class of disease

| pancreatic ductal adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7716 DOID:7716]

|

|

|

|-

| mixed endometrial stromal and smooth muscle tumor

| class of disease

| uterine corpus cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8302 DOID:8302]

|

|

|

|-

| mixed epithelial stromal tumour

| class of disease

| malignant mixed tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5088 DOID:5088]

|

|

|

|-

| mixed epithelial tumor of ovary

| class of disease

| ovarian benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6211 DOID:6211]

|

|

|

|-

| mixed epithelial/mesenchymal metaplastic breast carcinoma

| class of disease

| breast metaplastic carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7541 DOID:7541]

|

|

|

|-

| mixed extragonadal germ cell cancer

| class of disease

| mixed germ cell cancer

| mixed germ cell cancer that is located in areas of the body other than the ovary or testicle

| [http://www.disease-ontology.org/?id=DOID:0050907 DOID:0050907]

|

|

|

|-

| mixed fibrolamellar hepatocellular carcinoma

| class of disease

| fibrolamellar hepatocellular carcinoma

| fibrolamellar carcinoma that is characteirzed by the presence of both pure fibrolamellar hepatocellular carcinoma and conventional hepatocellular carcinoma components

| [http://www.disease-ontology.org/?id=DOID:0080182 DOID:0080182]

|

|

|

|-

| mixed germ cell cancer

| class of disease

| germ cell cancer

| germ cell cancer that occurs in many forms

| [http://www.disease-ontology.org/?id=DOID:3306 DOID:3306]

|

| Mixed germ cell neoplasia

|

|-

| mixed germ cell-sex cord neoplasm

| class of disease

| malignant mixed tumor
sex cord-gonadal stromal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2996 DOID:2996]

|

|

|

|-

| mixed glioma

| class of disease

| glioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5076 DOID:5076]

|

|

|

|-

| mixed gonadal dysgenesis X0/XY

| class of disease

| Turner syndrome
gonadal dysgenesis
disease

| intersex variation

| [http://www.disease-ontology.org/?id=DOID:14449 DOID:14449]
[http://www.disease-ontology.org/?id=DOID:0080656 DOID:0080656]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.706.316.309.391 C12.706.316.309.391]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.706.316.795.249 C12.706.316.795.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.875.253.309.391 C13.351.875.253.309.391]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.875.253.795.249 C13.351.875.253.795.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.260.830.835.249 C16.131.260.830.835.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.316.309.391 C16.131.939.316.309.391]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.939.316.795.249 C16.131.939.316.795.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.180.830.835.249 C16.320.180.830.835.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.119.309.391 C19.391.119.309.391]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.119.795.249 C19.391.119.795.249]

|

|

|-

| mixed hepatoblastoma

| class of disease

| hepatoblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5789 DOID:5789]

|

|

|

|-

| mixed lacrimal gland cancer

| class of disease

| lacrimal gland cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:296 DOID:296]

|

|

|

|-

| mixed liposarcoma

| class of disease

| liposarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5703 DOID:5703]

|

|

|

|-

| mixed malaria

| class of disease

| malaria

| malaria that involves infection with more than one species of Plasmodium at the same time

| [http://www.disease-ontology.org/?id=DOID:14325 DOID:14325]

|

|

|

|-

| mixed oligodendroglioma-astrocytoma

| class of disease

| mixed glioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7912 DOID:7912]

|

|

|

|-

| mixed phenotype acute leukemia with MLL rearranged

| class of disease

| acute biphenotypic leukaemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0081037 DOID:0081037]

|

|

|

|-

| mixed phenotype acute leukemia, B/myeloid

| class of disease

| acute biphenotypic leukaemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0081038 DOID:0081038]

|

|

|

|-

| mixed receptive-expressive language disorder

| class of disease

| communication disorder

| neurodevelopmental condition

| [http://www.disease-ontology.org/?id=DOID:12685 DOID:12685]

|

|

|

|-

| mixed sleep apnea

| class of disease

| sleep apnea

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080302 DOID:0080302]

|

|

|

|-

| mixed testicular germ cell tumor

| class of disease

| testicular malignant germ cell cancer
mixed germ cell cancer

| mixed germ cell cancer that is located in the testis

| [http://www.disease-ontology.org/?id=DOID:4743 DOID:4743]

|

|

|

|-

| mixed type rhabdomyosarcoma

| class of disease

| rhabdomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4065 DOID:4065]

|

|

|

|-

| mixed type thymoma

| class of disease

| thymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3280 DOID:3280]

|

|

|

|-

| mixed-type liposarcoma

| class of disease

| liposarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5709 DOID:5709]

|

|

|

|-

| mollusc allergy

| class of disease

| shellfish allergy

| shellfish allergy triggered by Mollusca

| [http://www.disease-ontology.org/?id=DOID:0060523 DOID:0060523]

|

|

|

|-

| molybdenum cofactor deficiency type A

| class of disease

| molybdenum cofactor deficiency
genetic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111164 DOID:0111164]

|

|

|

|-

| monoclonal gammopathy of uncertain significance

| class of disease

| monoclonal gammopathy
blood protein disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:7442 DOID:7442]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.147.542.640 C15.378.147.542.640]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.147.780.570 C15.378.147.780.570]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.460.640 C20.683.460.640]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.780.640 C20.683.780.640]

|

|

|-

| monoclonal paraproteinemia

| class of disease

| plasma protein metabolism disease
paraproteinemia
monoclonal gammopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2346 DOID:2346]

|

|

|

|-

| monocular esotropia

| class of disease

| esotropia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10293 DOID:10293]

|

|

|

|-

| monocular exotropia

| class of disease

| exotropia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11853 DOID:11853]

|

|

|

|-

| monocyte, dendritic cell, and NK cell deficiency

| class of disease

| combined immunodeficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111966 DOID:0111966]

|

|

|

|-

| monocytic leukemia

| class of disease

| myeloid leukemia

| type of myeloid leukemia characterized by a dominance of monocytes in the marrow

| [http://www.disease-ontology.org/?id=DOID:8527 DOID:8527]

|

|

|

|-

| monodermal teratoma

| class of disease

| ovarian germ cell teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5207 DOID:5207]

|

|

|

|-

| monofixation syndrome

| class of disease

| strabismus

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9843 DOID:9843]

|

| Monofixation syndrome

|

|-

| monogenic disease

| class of disease

| genetic disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050177 DOID:0050177]

|

|

|

|-

| mononeuritis

| class of disease

| mononeuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1802 DOID:1802]

|

|

|

|-

| mononeuritis multiplex

| class of disease

| mononeuritis of upper limb and mononeuritis multiplex

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1835 DOID:1835]

|

|

|

|-

| mononeuritis of lower limb

| class of disease

| mononeuritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9473 DOID:9473]

|

|

|

|-

| mononeuritis of upper limb

| class of disease

| mononeuritis of upper limb and mononeuritis multiplex

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1844 DOID:1844]

|

|

|

|-

| mononeuritis of upper limb and mononeuritis multiplex

| class of disease

| mononeuritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:572 DOID:572]

|

|

|

|-

| mononeuropathy

| class of disease

| peripheral neuropathy
disease

| neuropathy that is characterized by damage to a single nerve, which results in loss of movement, sensation, or other function of that nerve

| [http://www.disease-ontology.org/?id=DOID:1188 DOID:1188]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.500 C10.668.829.500]

|

|

|-

| monophasic synovial sarcoma

| class of disease

| synovial sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5495 DOID:5495]

|

|

|

|-

| mood disorder

| class of disease

| mental disorder

| any of various disorders characterised primarily by disturbance in an individual's mood

| [http://www.disease-ontology.org/?id=DOID:3324 DOID:3324]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.600 F03.600]

| Mood disorders

|

|-

| morbid obesity

| class of disease

| obesity

| human disease

| [http://www.disease-ontology.org/?id=DOID:11981 DOID:11981]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.654.726.500.700 C18.654.726.500.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.144.699.500.500 C23.888.144.699.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=E01.370.600.115.100.160.120.699.500.500 E01.370.600.115.100.160.120.699.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=G07.100.100.160.120.699.500.500 G07.100.100.160.120.699.500.500]

| Obesity

| File:Morbid Obesity.jpg

|-

| morpheaform basal cell carcinoma

| class of disease

| basal-cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4292 DOID:4292]

|

|

|

|-

| morphine dependence

| class of disease

| opiate dependence

| opiate dependence that involves the continued use of morphine despite despite problems related to use of the substance

| [http://www.disease-ontology.org/?id=DOID:2560 DOID:2560]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C25.775.675.600 C25.775.675.600]

|

|

|-

| mosaic variegated aneuploidy syndrome

| class of disease

| syndrome
aneuploidy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080688 DOID:0080688]

|

|

|

|-

| mosaic variegated aneuploidy syndrome 3

| class of disease

| autosomal recessive disease
mosaic variegated aneuploidy syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080689 DOID:0080689]

|

|

|

|-

| motility-related diarrhea

| class of disease

| diarrhea

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050131 DOID:0050131]

|

|

|

|-

| motor neuritis

| class of disease

| motor neuron disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:683 DOID:683]

|

|

|

|-

| motor neuron disease

| class of disease

| neurological disorder
neurodegeneration
disease

| group of neurological disorders affecting motor neurons

| [http://www.disease-ontology.org/?id=DOID:231 DOID:231]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.562 C10.574.562]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.467 C10.668.467]

| Motor neuron diseases

|

|-

| mouth cancer

| class of disease

| gastrointestinal system cancer
mouth disease
oral cavity neoplasm
head and neck cancer
disease

| gastrointestinal system cancer that is located in the oral cavity

| [http://www.disease-ontology.org/?id=DOID:8618 DOID:8618]

|

| Oral cancer

| File:ZungenCa2a.jpg

|-

| mouth disease

| class of disease

| gastrointestinal system disease
stomatognathic disease
disease of anatomical entity
disease

| gastrointestinal system disease that is located in the mouth

| [http://www.disease-ontology.org/?id=DOID:403 DOID:403]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465 C07.465]

| Diseases and disorders of oral cavity, salivary glands and jaws

|

|-

| movement disorders

| class of disease

| encephalopathy
motor dysfunction
disease

| clinical syndromes with either an excess of movement or a paucity of voluntary and involuntary movements

| [http://www.disease-ontology.org/?id=DOID:480 DOID:480]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.662 C10.228.662]

| Movement disorders

|

|-

| mpox

| class of disease
symptom or sign
notifiable disease

| viral infectious disease
Poxviridae infectious disease
zoonosis
disease

| viral disease

| [http://www.disease-ontology.org/?id=DOID:3292 DOID:3292]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.256.743.615 C01.925.256.743.615]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C22.735.750 C22.735.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C22.795.600 C22.795.600]

| Monkeypox

| File:Monkeypox.jpg

|-

| mu chain disease

| class of disease

| heavy chain disease

| heavy chain disease that results from an overproduction of mu antibody (IgM)

| [http://www.disease-ontology.org/?id=DOID:0060128 DOID:0060128]

|

|

|

|-

| mucin-rich endometrial endometrioid adenocarcinoma

| class of disease

| endometrial adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7293 DOID:7293]

|

|

|

|-

| mucinosis

| class of disease

| connective tissue disease
metabolic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3141 DOID:3141]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.550 C17.300.550]

| Mucinoses

|

|-

| mucinous adenocarcinoma

| class of disease

| adenocarcinoma

| adenocarcinoma that derives from epithelial cells originating in glandular tissue, which produce mucin

| [http://www.disease-ontology.org/?id=DOID:3030 DOID:3030]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.075 C04.557.470.200.025.075]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.590.075 C04.557.470.590.075]

| Pseudomyxoma peritonei

| File:Invasive mucinous adenocarcinoma Case 250 (8207252350).jpg

|-

| mucinous adenofibroma

| class of disease

| adenofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2700 DOID:2700]

|

|

|

|-

| mucinous cystadenocarcinoma

| class of disease

| cystadenocarcinoma
mucinous tumor

| cystadenocarcinoma that derives from epithelial cells originating in glandular tissue, with a capsulated structure and mucus-producing cells

| [http://www.disease-ontology.org/?id=DOID:3603 DOID:3603]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.480.225 C04.557.470.200.025.480.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.590.480.225 C04.557.470.590.480.225]

|

| File:Mucinous cystic tumor, atypical, uncertain malignant potential Case 252 (8211727496).jpg

|-

| mucinous cystadenocarcinoma of the lung

| class of disease

| adenocarcinoma of the lung
mucinous cystadenocarcinoma

| lung adenocarcinoma that is a very rare malignant mucus-producing neoplasm arising from the uncontrolled growth of transformed epithelial cells originating in lung tissue

| [http://www.disease-ontology.org/?id=DOID:0080304 DOID:0080304]

|

|

|

|-

| mucinous cystadenofibroma

| class of disease

| cystadenofibroma

| benign neoplasm characterized by the presence of cystic structures lined by mucinous columnar epithelial cells in a fibrotic stroma

| [http://www.disease-ontology.org/?id=DOID:6468 DOID:6468]

|

|

|

|-

| mucinous intrahepatic cholangiocarcinoma

| class of disease

| intrahepatic cholangiocarcinoma
bile duct mucinous adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7024 DOID:7024]

|

|

|

|-

| mucinous lung adenocarcinoma

| class of disease

| adenocarcinoma of the lung
mucinous adenocarcinoma

| lung adenocarcinoma with tumor cells floating in pools of mucin that distend alveolar spaces

| [http://www.disease-ontology.org/?id=DOID:0080303 DOID:0080303]

|

|

|

|-

| mucinous ovarian cystadenoma

| class of disease

| ovarian cystadenoma
mucinous cystadenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3267 DOID:3267]

|

| Mucinous cystoadenoma of the ovary

| File:Mucinous Cystadenoma of Ovary (218889489).jpg

|-

| mucinous pancreas adenocarcinoma

| class of disease

| pancreatic adenocarcinoma
mucinous adenocarcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080782 DOID:0080782]

|

|

|

|-

| mucinous stomach adenocarcinoma

| class of disease

| gastric diffuse adenocarcinoma
mucinous adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3716 DOID:3716]

|

|

|

|-

| mucinous tubular and spindle cell carcinoma

| class of disease

| renal cell carcinoma
tubulopathy
spindle cell carcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:4472 DOID:4472]

|

| Mucinous tubular and spindle cell carcinoma

| File:Renal Mucinous spindle 1.JPG

|-

| mucocele of appendix

| class of disease

| intestinal disease
mucocele

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13248 DOID:13248]

|

|

|

|-

| mucoepidermoid esophageal carcinoma

| class of disease

| esophageal carcinoma
mucoepidermoid carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4686 DOID:4686]

|

|

|

|-

| mucoepidermoid thyroid carcinoma

| class of disease

| thyroid carcinoma
mucoepidermoid carcinoma
thyroid gland adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4687 DOID:4687]

|

|

|

|-

| mucolipidosis type III gamma

| class of disease

| pseudo-Hurler polydystrophy
mucolipidosis
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080678 DOID:0080678]

|

|

|

|-

| mucopolysaccharidosis IV

| class of disease

|

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050808 DOID:0050808]

|

|

|

|-

| mucopolysaccharidosis Ih

| class of disease

| autosomal recessive disease
mucopolysaccharidosis I

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111390 DOID:0111390]

|

|

|

|-

| mucopolysaccharidosis Ih/s

| class of disease

| autosomal recessive disease
mucopolysaccharidosis I

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111389 DOID:0111389]

|

|

|

|-

| mucopolysaccharidosis type IIIA

| class of disease

| Sanfilippo syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111395 DOID:0111395]

|

|

|

|-

| mucopolysaccharidosis type IIIB

| class of disease

| Sanfilippo syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111394 DOID:0111394]

|

|

|

|-

| mucopolysaccharidosis type IIIC

| class of disease

| autosomal recessive disease
Sanfilippo syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111393 DOID:0111393]

|

|

|

|-

| mucopolysaccharidosis type IIID

| class of disease

| autosomal recessive disease
Sanfilippo syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111402 DOID:0111402]

|

|

|

|-

| mucopolysaccharidosis type IVA

| class of disease

| Morquio syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111391 DOID:0111391]

|

|

|

|-

| mucopolysaccharidosis type IVB

| class of disease

| autosomal recessive disease
Morquio syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111392 DOID:0111392]

|

|

|

|-

| mucormycosis

| class of disease
symptom or sign

| zygomycosis
opportunistic mycosis
disease

| fungal infection by the order Mucorales

| [http://www.disease-ontology.org/?id=DOID:8485 DOID:8485]
[http://www.disease-ontology.org/?id=DOID:0050595 DOID:0050595]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.703.980.600 C01.150.703.980.600]

|

| File:Periorbital fungal infection known as mucormycosis, or phycomycosis PHIL 2831 lores.jpg

|-

| mucosal melanoma

| class of disease

| melanoma
extracutaneous melanoma

| melanoma that has material basis in melanocytes located in mucosal membranes lining the respiratory, gastrointestinal and urogenital tract

| [http://www.disease-ontology.org/?id=DOID:0050929 DOID:0050929]

|

|

|

|-

| mucositis

| class of disease

| skin disease
gastrointestinal system disease

| gastrointestinal system disease that is characterized by painful inflammation and ulceration of the mucous membranes lining the digestive tract

| [http://www.disease-ontology.org/?id=DOID:0080178 DOID:0080178]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.798 C06.405.205.798]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.584 C07.465.584]

| Mucositis

|

|-

| multicentric papillary thyroid carcinoma

| class of disease

| papillary thyroid cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7086 DOID:7086]

|

|

|

|-

| multicentric reticulohistiocytosis

| class of disease

| Reticulohistiocytosis
syndrome

| syndrome that is characterized by papulonodular skin lesions containing a proliferation of true macrophages associated with arthritis

| [http://www.disease-ontology.org/?id=DOID:11824 DOID:11824]

|

|

|

|-

| multifocal dystonia

| class of disease

| dystonia

| dystonia that involves two or more unrelated body parts

| [http://www.disease-ontology.org/?id=DOID:0050837 DOID:0050837]

|

|

|

|-

| multifocal osteogenic sarcoma

| class of disease

| osteosarcoma
bone sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3360 DOID:3360]

|

|

|

|-

| multilocular cystic clear cell renal cell carcinoma

| class of disease

| renal cell carcinoma
renal clear cell carcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:4463 DOID:4463]

|

|

|

|-

| multiminicore disease

| class of disease

|

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080991 DOID:0080991]

|

|

|

|-

| multinodular goiter

| class of disease

| goiter
nodular goiter

| goiter characterized by a multinodular enlargement of the thyroid gland

| [http://www.disease-ontology.org/?id=DOID:0050489 DOID:0050489]

|

|

|

|-

| multiple benign circumferential skin creases on limbs

| class of disease

| skin disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112241 DOID:0112241]

|

|

|

|-

| multiple chemical sensitivity

| class of disease

| syndrome

| chronic medical condition of disputed but probably multifactorial etiology (genetic and non-genetic)

| [http://www.disease-ontology.org/?id=DOID:4661 DOID:4661]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.312.500 C20.543.312.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C21.223.500 C21.223.500]

| Multiple chemical sensitivity

|

|-

| multiple congenital anomalies-hypotonia-seizures syndrome

| class of disease

| lipid metabolism disorder

| lipid metabolism disorder that is characterized by phosphatidylinositol glycan anchor biosynthesis class A (PIGA) deficiency

| [http://www.disease-ontology.org/?id=DOID:0080503 DOID:0080503]

|

|

|

|-

| multiple cranial nerve palsy

| class of disease

| glossopharyngeal nerve disease
cranial nerve disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13866 DOID:13866]

|

|

|

|-

| multiple endocrine neoplasia

| class of disease

| endocrine gland neoplasm
multiple polyglandular tumor

| human disease

| [http://www.disease-ontology.org/?id=DOID:3125 DOID:3125]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.400 C04.588.322.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.651.600 C04.651.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.700.630 C04.700.630]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.700.630 C16.320.700.630]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.400 C19.344.400]

| Multiple endocrine neoplasia

|

|-

| multiple epiphyseal dysplasia 2

| class of disease

| multiple epiphyseal dysplasia
genetic disease
autosomal dominant disease
multiple epiphyseal dysplasia due to collagen 9 anomaly

| multiple epiphyseal dysplasia due to collagen 9 anomaly that has material basis in heterozygous mutation in the COL9A2 gene on chromosome 1p34

| [http://www.disease-ontology.org/?id=DOID:0070298 DOID:0070298]

|

|

|

|-

| multiple epiphyseal dysplasia 3

| class of disease

| multiple epiphyseal dysplasia
genetic disease
multiple epiphyseal dysplasia due to collagen 9 anomaly
autosomal dominant disease

| multiple epiphyseal dysplasia due to collagen 9 anomaly that has material basis in heterozygous mutation in the COL9A3 gene on chromosome 20q13

| [http://www.disease-ontology.org/?id=DOID:0070304 DOID:0070304]

|

|

|

|-

| multiple epiphyseal dysplasia 7

| class of disease

| multiple epiphyseal dysplasia
genetic disease
autosomal recessive disease

| multiple epiphyseal dysplasia that has material basis in homozygous mutation in the CANT1 gene on chromosome 17q25

| [http://www.disease-ontology.org/?id=DOID:0070302 DOID:0070302]

|

|

|

|-

| multiple epiphyseal dysplasia due to collagen 9 anomaly

| class of disease

| multiple epiphyseal dysplasia
genetic disease
monogenic disease

| multiple epiphyseal dysplasia that has material basis in mutation in any of the members of the COL9A gene family (COL9A1, COL9A2, COL9A3)

| [http://www.disease-ontology.org/?id=DOID:0070305 DOID:0070305]

|

|

|

|-

| multiple epiphyseal dysplasia with myopia and deafness

| class of disease

| syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111348 DOID:0111348]

|

|

|

|-

| multiple mitochondrial dysfunctions syndrome 6

| class of disease

| fatal multiple mitochondrial dysfunctions syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070332 DOID:0070332]

|

|

|

|-

| multiple mucosal neuroma

| class of disease

| neuroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5155 DOID:5155]

|

|

|

|-

| multiple myeloma

| class of disease

| leukocyte disease
myeloid neoplasm
immunoproliferative disorder
disease

| cancer of plasma cells

| [http://www.disease-ontology.org/?id=DOID:9538 DOID:9538]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.595.500 C04.557.595.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.907.454.460 C14.907.454.460]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.147.780.650 C15.378.147.780.650]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.463.515.460 C15.378.463.515.460]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.845 C20.683.515.845]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.780.650 C20.683.780.650]

| Multiple myeloma

| File:Plasmozytom multiple Osteolysen Unterarm.png

|-

| multiple spinal canal and spinal cord meningioma

| class of disease

| spinal canal and spinal cord meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7646 DOID:7646]

|

|

|

|-

| multisystem proteinopathy

| class of disease

| motor neuron disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:070355 DOID:070355]

|

|

|

|-

| mumps

| class of disease
symptom or sign

| parotitis
mumps virus infectious disease
herpangina
salivary gland disease
disease

| Human disease caused by paramyxovirus

| [http://www.disease-ontology.org/?id=DOID:10264 DOID:10264]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.782.580.600.680.500 C01.925.782.580.600.680.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.815.470.800.630 C07.465.815.470.800.630]

| Mumps

| File:Mumps.jpg

|-

| muscle neoplasm

| class of disease

| soft tissue neoplasm
muscular disease

| tumors or cancer located in muscle tissue or specific muscles

| [http://www.disease-ontology.org/?id=DOID:461 DOID:461]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.839.500 C04.588.839.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.494 C05.651.494]

|

|

|-

| muscle tissue disease

| class of disease

| muscular disease

| disease involving the muscle tissue

| [http://www.disease-ontology.org/?id=DOID:66 DOID:66]

|

|

|

|-

| muscular atrophy

| class of disease

| muscular disease
atrophic muscular disease
clinical sign

| human disease

| [http://www.disease-ontology.org/?id=DOID:767 DOID:767]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.613.612 C10.597.613.612]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.300.070.500 C23.300.070.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.608.612 C23.888.592.608.612]

| Muscle wasting

|

|-

| musculoskeletal disorder

| class of disease

| disease of anatomical entity

| disease of anatomical entity that occurs in the muscular and/or skeletal system

| [http://www.disease-ontology.org/?id=DOID:17 DOID:17]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05 C05]

| Diseases and disorders of the musculoskeletal system

| File:Ankle Joint Arthritis.jpg

|-

| musculoskeletal system benign neoplasm

| class of disease

| organ system benign neoplasm
musculoskeletal neoplasm

| organ system benign neoplasm that is located in the muscular and skeletal organs

| [http://www.disease-ontology.org/?id=DOID:0060099 DOID:0060099]

|

|

|

|-

| musculoskeletal system cancer

| class of disease

| organ system cancer
musculoskeletal disorder
musculoskeletal neoplasm

| organ system cancer located in the muscular and skeletal organs and characterized by uncontrolled cellular proliferation of the musculoskeletal organs

| [http://www.disease-ontology.org/?id=DOID:0060100 DOID:0060100]

|

|

|

|-

| mushroom workers' lung

| class of disease

| extrinsic allergic alveolitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2708 DOID:2708]

|

|

|

|-

| mycoplasma infection

| class of disease

| bacterial infectious disease
primary Mycoplasmataceae infectious disease
disease

| bacterial infection with a species of the genus Mycoplasma

| [http://www.disease-ontology.org/?id=DOID:0050407 DOID:0050407]
[http://www.disease-ontology.org/?id=DOID:5461 DOID:5461]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.400.610.610 C01.150.252.400.610.610]

|

|

|-

| mycosis fungoides

| class of disease

| cutaneous T cell lymphoma
rare disease
mycosis fungoides and variants
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8691 DOID:8691]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386.480.750.800.550 C04.557.386.480.750.800.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.569.480.750.800.550 C15.604.515.569.480.750.800.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.761.480.750.800.550 C20.683.515.761.480.750.800.550]

| Mycosis fungoides

| File:Mycosis fungoides knee.JPG

|-

| mycotic corneal ulcer

| class of disease

| corneal ulcer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10440 DOID:10440]

|

|

|

|-

| myelitis

| class of disease

| spinal cord disease

| spinal cord disease that is characterized by inflammation of the white matter or gray matter of the spinal cord

| [http://www.disease-ontology.org/?id=DOID:322 DOID:322]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.228.618 C10.228.228.618]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.854.525 C10.228.854.525]

| Myelitis

| File:Living anatomy and pathology; (1910) (14571685858).jpg

|-

| myelodysplastic syndrome

| class of disease

| myeloproliferative disorders
neoplastic syndrome
disease

| diverse collection of blood-related medical conditions with ineffective production of the myeloid class of blood cells

| [http://www.disease-ontology.org/?id=DOID:0050908 DOID:0050908]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.190.625 C15.378.190.625]

| Myelodysplastic syndrome

|

|-

| myelodysplastic/myeloproliferative neoplasm

| class of disease

| myeloid neoplasm

| myeloid neoplasm that results in the overproduction of white blood cells

| [http://www.disease-ontology.org/?id=DOID:4972 DOID:4972]

|

|

|

|-

| myelofibrosis

| class of disease

| myeloid neoplasm
acquired aplastic anemia
rare genetic immune disease
disease

| myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue

| [http://www.disease-ontology.org/?id=DOID:4971 DOID:4971]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.190.636.765 C15.378.190.636.765]

|

| File:Myelofibrosis, Reticulin Stain (6032644716).jpg

|-

| myeloid and lymphoid neoplasms associated with FGFR1 abnormalities

| class of disease

| myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1

| myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the FGFR1 gene, resulting in translocations with an 8p11 breakpoint

| [http://www.disease-ontology.org/?id=DOID:0080167 DOID:0080167]

|

|

|

|-

| myeloid and lymphoid neoplasms associated with PDGFRA rearrangement

| class of disease

| myeloid neoplasm associated with PDGFRA rearrangement
myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1

| myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the PDGFRA gene, most often resulting in the formation of FIP1L1-PDGFRA fusion transcripts

| [http://www.disease-ontology.org/?id=DOID:0080165 DOID:0080165]

|

|

|

|-

| myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1

| class of disease

| myeloid neoplasm
myeloid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB or FGFR1

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080164 DOID:0080164]

|

|

|

|-

| myeloid leukemia

| class of disease

| leukemia
disease

| leukemia that is located in myeloid tissue

| [http://www.disease-ontology.org/?id=DOID:8692 DOID:8692]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.539 C04.557.337.539]

| Myeloid leukemias

|

|-

| myeloid leukemia associated with Down Syndrome

| class of disease

| acute megakaryoblastic leukemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080798 DOID:0080798]

|

|

|

|-

| myeloid neoplasm

| class of disease

| myeloproliferative disorders

| a bone marrow cancer that is formed of any one of the bone marrow cells belonging to the granulocytic (neutrophil, eosinophil, basophil), monocytic/macrophage, erythroid, megakaryocytic and mast cell lineages.

| [http://www.disease-ontology.org/?id=DOID:0070004 DOID:0070004]

|

|

|

|-

| myeloid neoplasms associated with PDGFRB rearrangement

| class of disease

| myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1

| myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 that is characterized by the rearrangement of the PDGFRB gene, most often resulting in the formation of ETV6-PDGFRB fusion transcripts

| [http://www.disease-ontology.org/?id=DOID:0080166 DOID:0080166]

|

|

|

|-

| myeloid sarcoma

| class of disease

| hematologic cancer

| solid tumor composed of immature white blood cells[2] called myeloblasts.

| [http://www.disease-ontology.org/?id=DOID:8683 DOID:8683]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.337.539.775 C04.557.337.539.775]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.853 C04.557.450.795.853]

| Myeloid sarcoma

|

|-

| myelophthisic anemia

| class of disease

| aplastic anemia

| aplastic anemia that is characterized by displacement of hemopoietic bone-marrow tissue either by fibrosis, tumors or granulomas

| [http://www.disease-ontology.org/?id=DOID:2354 DOID:2354]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.307 C15.378.071.307]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.190.636.085 C15.378.190.636.085]

|

|

|-

| myeloproliferative disorder, chronic, with eosinophilia

| class of disease

| myeloproliferative disorders
eosinophilia
myeloproliferative neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111344 DOID:0111344]

|

|

|

|-

| myeloproliferative disorders

| class of disease

| bone marrow disease
tumor of hematopoietic and lymphoid tissues
connective tissue neoplasm
hematologic cancer
disease

| hematopoietic disorders that derive from the blood-forming stem cells of the bone marrow

| [http://www.disease-ontology.org/?id=DOID:4960 DOID:4960]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.190.636 C15.378.190.636]

| Myeloid neoplasms

|

|-

| myeloproliferative neoplasm

| class of disease

| myeloid neoplasm
myeloproliferative disorders

| myeloid neoplasm that is characterized by a group of slow growing blood cancers in which large numbers of abnormal red blood cells, white blood cells, or platelets grow and spread in the bone marrow and the peripheral blood

| [http://www.disease-ontology.org/?id=DOID:2226 DOID:2226]

|

|

|

|-

| myoblastoma

| class of disease

| muscle neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:5039 DOID:5039]

|

|

|

|-

| myocardial stunning

| class of disease

| myocardial infarction

| state when some section of the myocardium (corresponding to area of a major coronary occlusion) shows a form of contractile abnormality

| [http://www.disease-ontology.org/?id=DOID:9767 DOID:9767]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.671 C14.280.671]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.582 C23.888.582]

|

|

|-

| myocarditis

| class of disease
symptom or sign

| extrinsic cardiomyopathy
myocardial disorder
pancarditis
cardiovascular system symptom
disease

| extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle

| [http://www.disease-ontology.org/?id=DOID:820 DOID:820]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.238.625 C14.280.238.625]

| Myocarditis

| File:Viral myocarditis (1).JPG

|-

| myocardium cancer

| class of disease

| neoplasm of myocardium
heart cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:9299 DOID:9299]

|

|

|

|-

| myoclonic cerebellar dyssynergia

| class of disease

| neurodegeneration
nervous system heredodegenerative disease
Ramsay Hunt syndrome

| degenerative, neurological disorder characterized by myoclonus epilepsy, intention tremor, progressive ataxia and occasionally cognitive impairment

| [http://www.disease-ontology.org/?id=DOID:12707 DOID:12707]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.252.700.250 C10.228.140.252.700.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.854.787.500 C10.228.854.787.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.500.825.250 C10.574.500.825.250]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.400.780.500 C16.320.400.780.500]

|

|

|-

| myoclonic dystonia 11

| class of disease

| myoclonic dystonia
genetic disease
autosomal dominant disease

| myoclonic dystonia characterized by autosomal dominant inheritance and association with psychiatric disorder that has material basis in heterozygous mutation in the SGCE gene on chromosome 7q21

| [http://www.disease-ontology.org/?id=DOID:0090034 DOID:0090034]

|

|

|

|-

| myoclonic dystonia 15

| class of disease

| myoclonic dystonia
genetic disease
autosomal dominant disease

| myoclonic dystonia characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 18p11

| [http://www.disease-ontology.org/?id=DOID:0090035 DOID:0090035]

|

|

|

|-

| myoepithelial carcinoma

| class of disease

| carcinoma

| carcinoma that derives from myoepithelial cells

| [http://www.disease-ontology.org/?id=DOID:4838 DOID:4838]

|

|

|

|-

| myoepithelioma of the head and neck

| class of disease

| sweat gland neoplasm

| neoplasm composed of outgrowths of myoepithelial cells from a sweat gland

| [http://www.disease-ontology.org/?id=DOID:2661 DOID:2661]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.435.585 C04.557.435.585]

| Myoepithelioma of the head and neck

|

|-

| myofascial pain syndrome

| class of disease

| muscular disease
medically unexplained physical symptom
myalgia
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:431 DOID:431]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.550 C05.651.550]

|

|

|-

| myofibrillar myopathy

| class of disease

| muscular disease

| myopathy that is characterized by slowly progressive muscle weakness that can involve both proximal muscles and distal muscles

| [http://www.disease-ontology.org/?id=DOID:0080307 DOID:0080307]

|

|

|

|-

| myofibrillar myopathy 10

| class of disease

| autosomal recessive disease
myofibrillar myopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112108 DOID:0112108]

|

|

|

|-

| myofibrillar myopathy 3

| class of disease

| myofibrillar myopathy
autosomal dominant disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0080094 DOID:0080094]

|

|

|

|-

| myofibroma

| class of disease

| connective tissue neoplasm
benign perivascular tumor
connective tissue benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4386 DOID:4386]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.540 C04.557.450.565.540]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.680.540 C17.300.680.540]

|

| File:Lipoleiomyoma uterus.jpg

|-

| myoma

| class of disease

| muscle neoplasm
uterine benign neoplasm
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:2691 DOID:2691]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.590.540 C04.557.450.590.540]

| Uterine fibroids

| File:Uterine fibroids.jpg

|-

| myopathy of extraocular muscle

| class of disease

| peripheral neuropathy
rare eye disease
muscular disease

| myopathy that involves the extra-ocular muscle

| [http://www.disease-ontology.org/?id=DOID:929 DOID:929]

|

|

|

|-

| myopathy, lactic acidosis, and sideroblastic anemia 1

| class of disease

| myopathy, lactic acidosis, and sideroblastic anemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111185 DOID:0111185]

|

|

|

|-

| myopathy, lactic acidosis, and sideroblastic anemia 2

| class of disease

| myopathy, lactic acidosis, and sideroblastic anemia

| A myopathy, lactic acidosis, and sideroblastic anemia characterized by marked phenotypic variablity in time of onset and severity of symptoms that has material basis in homozyous or compound heterozygous mutation in YARS2 on 12p11.21.

| [http://www.disease-ontology.org/?id=DOID:0111186 DOID:0111186]

|

|

|

|-

| myopathy, lactic acidosis, and sideroblastic anemia 3

| class of disease

| myopathy, lactic acidosis, and sideroblastic anemia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111184 DOID:0111184]

|

|

|

|-

| myopathy, myofibrillar, 11

| class of disease

| myofibrillar myopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0081338 DOID:0081338]

|

|

|

|-

| myopia

| class of disease
symptom or sign

| refractive error
visual impairment
disease

| visual defect which causes to see the near objects clearly and far objects unclearly

| [http://www.disease-ontology.org/?id=DOID:11830 DOID:11830]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.744.636 C11.744.636]

| Myopia

| File:Myopia.gif

|-

| myosarcoma

| class of disease

| musculoskeletal system cancer
muscle tissue neoplasm
muscular disease

| musculoskeletal system cancer that is located in muscle

| [http://www.disease-ontology.org/?id=DOID:4045 DOID:4045]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.590.550 C04.557.450.590.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.550 C04.557.450.795.550]

|

|

|-

| myositis

| class of disease

| muscular disease
inflammation
disease

| myopathy characterized by muscle inflammation

| [http://www.disease-ontology.org/?id=DOID:633 DOID:633]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.594 C05.651.594]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.491.562 C10.668.491.562]

|

|

|-

| myositis fibrosa

| class of disease

| myositis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9788 DOID:9788]

|

|

|

|-

| myositis ossificans

| class of disease

| myositis
heterotopic ossification

| myositis that is accompanied by ossification of muscle tissue or bony deposits in the muscles

| [http://www.disease-ontology.org/?id=DOID:668 DOID:668]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.594.638 C05.651.594.638]

|

|

|-

| myotonic cataract

| class of disease

| cataract

| Human disease

| [http://www.disease-ontology.org/?id=DOID:82 DOID:82]

|

|

|

|-

| myotonic disease

| class of disease

| muscular dystrophy

| muscular dystrophy characterized by progressive muscle wasting and weakness

| [http://www.disease-ontology.org/?id=DOID:450 DOID:450]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.651.662 C05.651.662]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.491.606 C10.668.491.606]

|

|

|-

| myringitis bullosa hemorrhagica

| class of disease

| tympanic membrane disease
disease

| tympanic membrane disease that is characterized by blisters on the eardrum resulting from infection

| [http://www.disease-ontology.org/?id=DOID:13791 DOID:13791]

|

|

|

|-

| myxedema

| class of disease

| hypothyroidism
mucinosis
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11634 DOID:11634]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.550.590 C17.300.550.590]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.874.482.638 C19.874.482.638]

| Myxedema

|

|-

| myxofibrosarcoma

| class of disease

| fibrous histiocytoma
skeletal muscle cancer
rare nervous system tumor
peripheral neuropathy
fibrosarcoma
fibromyxoid tumor
sarcoma

| A malignant fibroblastic neoplasm arising from the soft tissue. It is characterized by the presence of spindle-shaped cells, cellular pleomorphism, thin-walled blood vessels, fibrous septa, and myxoid stroma.

| [http://www.disease-ontology.org/?id=DOID:0080534 DOID:0080534]

|

|

|

|-

| myxoid chondrosarcoma

| class of disease

| chondrosarcoma
myxoid tumor

| human disease

| [http://www.disease-ontology.org/?id=DOID:5861 DOID:5861]

|

|

|

|-

| myxoid leiomyosarcoma

| class of disease

| leiomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5268 DOID:5268]

|

|

|

|-

| myxoid liposarcoma of the ovary

| class of disease

| liposarcoma of the ovary
myxoid liposarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8023 DOID:8023]

|

|

|

|-

| myxomatous pattern testicular yolk sac tumor

| class of disease

| testicular yolk sac tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8081 DOID:8081]

|

|

|

|-

| myxopapillary ependymoma

| class of disease

| benign ependymoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:5075 DOID:5075]

|

|

|

|-

| myxosarcoma

| class of disease

| sarcoma
connective tissue neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:4136 DOID:4136]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.560 C04.557.450.565.560]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.560 C04.557.450.795.560]

|

|

|-

| nail disease

| class of disease

| integumentary system disease

| integumentary system disease that is located in nail

| [http://www.disease-ontology.org/?id=DOID:4123 DOID:4123]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.529 C17.800.529]

| Diseases and disorders of the nails

|

|-

| nanophthalmos

| class of disease

| microphthalmia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080634 DOID:0080634]

|

|

|

|-

| narcissistic personality disorder

| class of disease

| personality disorder
narcissism
disease

| personality disorder that involves an excessive preoccupation with issues of personal adequacy, power, prestige and vanity

| [http://www.disease-ontology.org/?id=DOID:2745 DOID:2745]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.675.500 F03.675.500]

| Narcissistic personality disorder

| File:Seesaw narcissism megalomania model.png

|-

| narcolepsy

| class of disease

| disease
sleep disorder
excessive daytime sleepiness

| Human sleep disorder that involves an excessive urge to sleep and other neurological features

| [http://www.disease-ontology.org/?id=DOID:8986 DOID:8986]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.886.425.800.200.750 C10.886.425.800.200.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.870.400.800.200.750 F03.870.400.800.200.750]

| Narcolepsy

|

|-

| nasal cavity cancer

| class of disease

| sensory system cancer
nasal cancer
nasal cavity neoplasm
nasal cavity disease
respiratory system cancer

| respiratory system cancer that is located in the nasal cavity

| [http://www.disease-ontology.org/?id=DOID:10811 DOID:10811]

|

|

|

|-

| nasal cavity disease

| class of disease

| nose disease

| respiratory disease

| [http://www.disease-ontology.org/?id=DOID:2163 DOID:2163]

|

|

|

|-

| nasal cavity lymphoma

| class of disease

| nasal cavity cancer
lymphoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:10813 DOID:10813]

|

|

|

|-

| nasal cavity olfactory neuroblastoma

| class of disease

| nasal cavity cancer
esthesioneuroblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10812 DOID:10812]

|

|

|

|-

| nasopharyngeal disease

| class of disease

| upper respiratory tract disease
pharyngeal diseases

| respiratory disease

| [http://www.disease-ontology.org/?id=DOID:9561 DOID:9561]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.550.350 C07.550.350]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.775.350 C09.775.350]

|

|

|-

| nasopharyngitis

| class of disease

| nasopharyngeal disease

| respiratory disease

| [http://www.disease-ontology.org/?id=DOID:10460 DOID:10460]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.550.350.700 C07.550.350.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.550.781.500 C07.550.781.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.730.561.500 C08.730.561.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.775.350.700 C09.775.350.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.775.649.500 C09.775.649.500]

|

|

|-

| natural killer cell leukemia

| class of disease

| lymphoblastic leukemia
leukocyte disease
rare bone disease
immune disorder
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1035 DOID:1035]

|

|

|

|-

| near-fatal asthma

| class of disease

| acute asthma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080823 DOID:0080823]

|

|

|

|-

| necrobiosis lipoidica

| class of disease

| skin disease
diabetic dermadrome
necrobiotic disorders

| human disease

| [http://www.disease-ontology.org/?id=DOID:3486 DOID:3486]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.200.495.545 C17.300.200.495.545]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.550.545 C17.800.550.545]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.849.495 C17.800.849.495]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.880.495 C18.452.880.495]

| Necrobiosis lipoidica

| File:Necrobiosislipoidica.jpg

|-

| necrosis of ear ossicle

| class of disease

| middle ear disease
ear disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11783 DOID:11783]

|

|

|

|-

| necrosis of pituitary

| class of disease

| pituitary gland disease

| endocrine disease

| [http://www.disease-ontology.org/?id=DOID:3646 DOID:3646]

|

|

|

|-

| necrotizing enterocolitis

| class of disease

| gastrointestinal system disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:8677 DOID:8677]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.596.700 C06.405.205.596.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.363.700 C06.405.469.363.700]

| Neonatal necrotizing enterocolitis

|

|-

| necrotizing fasciitis

| class of disease
symptom or sign

| fasciitis
necrotizing soft tissue infection
disease

| infection that results in the death of the body's soft tissue

| [http://www.disease-ontology.org/?id=DOID:9602 DOID:9602]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.252.825.340 C01.252.825.340]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.321.550 C05.321.550]

| Necrotizing fasciitis

| File:Necrotizing fasciitis left leg.JPEG

|-

| necrotizing gastritis

| class of disease

| gastritis
necrosis
chronic gastritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4037 DOID:4037]

|

|

|

|-

| necrotizing sialometaplasia

| class of disease

| salivary gland disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12901 DOID:12901]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.815.802 C07.465.815.802]

| Necrotizing sialometaplasia

|

|-

| nemaline myopathy 2

| class of disease

| nemaline myopathy
genetic disease
autosomal recessive disease

| nemaline myopathy that has material basis in homozygous or compound heterozygous mutation in the NEB gene on chromosome 2q23

| [http://www.disease-ontology.org/?id=DOID:0110928 DOID:0110928]

|

|

|

|-

| nemaline myopathy 3

| class of disease

| nemaline myopathy
genetic disease
autosomal recessive disease

| nemaline myopathy that has material basis in homozygous, compound heterozygous, or heterozygous mutation in the ACTA1 gene on chromosome 1q42

| [http://www.disease-ontology.org/?id=DOID:0110927 DOID:0110927]

|

|

|

|-

| neomycin sulfate allergic contact dermatitis

| class of disease

| allergic contact dermatitis
drug allergy

| allergic contact dermatitis that has allergic trigger neomycin sulfate

| [http://www.disease-ontology.org/?id=DOID:0040067 DOID:0040067]

|

|

|

|-

| neonatal anemia

| class of disease

| anemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11244 DOID:11244]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.071.363 C15.378.071.363]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.614.053 C16.614.053]

|

|

|-

| neonatal diabetes mellitus

| class of disease

| diabetes
neonatal metabolic disturbances
rare genetic diabetes mellitus

| It is a congenital form of diabetes

| [http://www.disease-ontology.org/?id=DOID:11717 DOID:11717]

|

|

|

|-

| neonatal infective mastitis

| class of disease

| mastitis
perinatal infectious disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13520 DOID:13520]

|

|

|

|-

| neonatal jaundice

| class of disease

| pigmentation disorder
jaundice
neonatal hyperbilirubinemia
disease

| pigmentation disease characterized by a high level of bilirubin in the blood, causing a yellowing of the skin and other tissues of a newborn infant

| [http://www.disease-ontology.org/?id=DOID:2383 DOID:2383]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.614.451.500 C16.614.451.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.429.249.500 C23.550.429.249.500]

| Neonatal jaundice

| File:Jaundice phototherapy.jpg

|-

| neonatal leukemia

| class of disease

| childhood leukemia
perinatal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7756 DOID:7756]

|

|

|

|-

| neonatal myasthenia gravis

| class of disease

| myasthenia gravis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14043 DOID:14043]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.114.656.650 C10.114.656.650]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.758.725.650 C10.668.758.725.650]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.111.258.500.650 C20.111.258.500.650]

|

|

|-

| neonatal period electroclinical syndrome

| class of disease

| electroclinical syndrome
perinatal disease

| electroclinical syndrome with onset in the neonatal period less than 44 weeks of gestational age

| [http://www.disease-ontology.org/?id=DOID:0050702 DOID:0050702]

|

|

|

|-

| neonatal thyrotoxicosis

| class of disease

| thyrotoxicosis

| endocrine disease

| [http://www.disease-ontology.org/?id=DOID:12573 DOID:12573]

|

|

|

|-

| neonatal urinary tract infectious disease

| class of disease

| urinary system disease
urinary tract infection in children
perinatal infectious disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1375 DOID:1375]

|

|

|

|-

| neonatal-onset type II citrullinemia

| class of disease

| citrullinemia
autosomal recessive disease
citrullinemia type II

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070341 DOID:0070341]

|

|

|

|-

| neovascular glaucoma

| class of disease

| glaucoma
glaucoma associated with vascular disorder
rare acquired eye disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1687 DOID:1687]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.525.381.348 C11.525.381.348]

|

|

|-

| nephritis

| class of disease
symptom or sign

| urological symptom
disease

| inflammation of the kidneys

| [http://www.disease-ontology.org/?id=DOID:10952 DOID:10952]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.419.570 C12.777.419.570]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.419.570 C13.351.968.419.570]

| Nephritis

| File:Diffuse proliferative lupus nephritis.jpg

|-

| nephrocalcinosis

| class of disease

| kidney disease
calcinosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12679 DOID:12679]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.968.419.590 C12.050.351.968.419.590]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.777.419.590 C12.200.777.419.590]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.174.130.560 C18.452.174.130.560]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.950.419.590 C12.950.419.590]

| Nephrocalcinosis

|

|-

| nephrogenic adenofibroma

| class of disease

| kidney benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2698 DOID:2698]

|

|

|

|-

| nephrogenic adenoma of the urethra

| class of disease

| urethral benign neoplasm
nephrogenic adenoma
adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8109 DOID:8109]

|

|

|

|-

| nephrogenic adenoma of urinary bladder

| class of disease

| bladder benign neoplasm
nephrogenic adenoma
adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7333 DOID:7333]

|

|

|

|-

| nephrogenic diabetes insipidus type 2

| class of disease

| autosomal dominant disease
nephrogenic diabetes insipidus
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0081061 DOID:0081061]

|

|

|

|-

| nephrolithiasis

| class of disease

| kidney disease
kidney stone disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:585 DOID:585]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.777.419.600 C12.200.777.419.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.777.967.249 C12.200.777.967.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.968.419.600 C12.050.351.968.419.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.968.967.249 C12.050.351.968.967.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.950.419.600 C12.950.419.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.950.967.249 C12.950.967.249]

|

|

|-

| nephroma

| class of disease

| kidney benign neoplasm
kidney cortex disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080615 DOID:0080615]

|

|

|

|-

| nephronophthisis

| class of disease

| autosomal recessive disease
medullary cystic kidney disease
kidney disease

| congenital disorder of urinary system

| [http://www.disease-ontology.org/?id=DOID:12712 DOID:12712]

|

| Nephronophthisis

|

|-

| nephronophthisis 1

| class of disease

| nephronophthisis

| nephronophthisis that has material basis in homozygous or compound heterozygous mutation in or deletion of the NPHP1 gene on chromosome 2q13

| [http://www.disease-ontology.org/?id=DOID:0111112 DOID:0111112]

|

|

|

|-

| nephropathia epidemica

| class of disease

| hemorrhagic fever with renal syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050201 DOID:0050201]

|

|

|

|-

| nephrosclerosis

| class of disease

| renal hypertension
disease

| medical condition referring to damage to the kidney due to chronic high blood pressure

| [http://www.disease-ontology.org/?id=DOID:11664 DOID:11664]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.419.610 C12.777.419.610]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.419.610 C13.351.968.419.610]

|

|

|-

| nephrosis

| class of disease

| proteinuria
kidney disease

| non-inflammatory kidney disease

| [http://www.disease-ontology.org/?id=DOID:2527 DOID:2527]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.419.630 C12.777.419.630]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.419.630 C13.351.968.419.630]

| Nephrosis

|

|-

| nephrotic syndrome 14

| class of disease

| familial nephrotic syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080265 DOID:0080265]

|

|

|

|-

| nephrotic syndrome 15

| class of disease

| familial nephrotic syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080271 DOID:0080271]

|

|

|

|-

| nephrotic syndrome 16

| class of disease

| familial nephrotic syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080272 DOID:0080272]

|

|

|

|-

| nephrotic syndrome type 1

| class of disease

| familial nephrotic syndrome
autosomal recessive disease

| familial nephrotic syndrome characterized by prenatal onset of massive proteinuria followed by steroid resistant renal disease that has material basis in homozygous or compound heterozygous mutation in the NPHS1 gene on chromosome 19q13

| [http://www.disease-ontology.org/?id=DOID:0080390 DOID:0080390]

|

|

|

|-

| nephrotic syndrome type 17

| class of disease

| familial nephrotic syndrome
autosomal recessive disease

| familial nephrotic syndrome that has material basis in by homozygous or compound heterozygous mutation in the NUP85 gene on chromosome 17q25

| [http://www.disease-ontology.org/?id=DOID:0080392 DOID:0080392]

|

|

|

|-

| nephrotic syndrome type 18

| class of disease

| familial nephrotic syndrome
autosomal recessive disease

| familial nephrotic syndrome that has material basis in by homozygous or compound heterozygous mutation in the NUP133 gene on chromosome 1q42

| [http://www.disease-ontology.org/?id=DOID:0080393 DOID:0080393]

|

|

|

|-

| nephrotic syndrome type 19

| class of disease

| familial nephrotic syndrome
autosomal recessive disease

| familial nephrotic syndrome that has material basis in compound heterozygous mutation in the NUP160 gene on chromosome 11p11

| [http://www.disease-ontology.org/?id=DOID:0080394 DOID:0080394]

|

|

|

|-

| nephrotic syndrome type 2

| class of disease

| familial nephrotic syndrome
autosomal recessive disease
nephrotic syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080379 DOID:0080379]

|

|

|

|-

| nephrotic syndrome type 20

| class of disease

| familial nephrotic syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070357 DOID:0070357]

|

|

|

|-

| nephrotic syndrome type 22

| class of disease

| familial nephrotic syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112268 DOID:0112268]

|

|

|

|-

| nephrotic syndrome type 3

| class of disease

| familial nephrotic syndrome
autosomal recessive disease

| familial nephrotic syndrome characterized by early childhood onset, steroid restance and diffuse mesangial sclerosis in most patients that has material basis in homozygous or compound heterozygous mutation in the PLCE1 gene on chromosome 10q23

| [http://www.disease-ontology.org/?id=DOID:0080382 DOID:0080382]

|

|

|

|-

| nephrotic syndrome type 5

| class of disease

| familial nephrotic syndrome
autosomal recessive disease

| familial nephrotic syndrome characterized by prenatal or neonatal onset of progressive renal failure with proteinurea and edema that has material basis in homozygous or compound heterozygous mutation in the LAMB2 gene on chromosome 3p

| [http://www.disease-ontology.org/?id=DOID:0080380 DOID:0080380]

|

|

|

|-

| nephrotic syndrome type 7

| class of disease

| familial nephrotic syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080388 DOID:0080388]

|

|

|

|-

| nephrotic syndrome type 8

| class of disease

| familial nephrotic syndrome
autosomal recessive disease

| familial nephrotic syndrome characterized by neonatal or early childhood onset steroid resistant renal disease that has material basis in homozygous or compound heterozygous mutation in the ARHGDIA gene on chromosome 17q25

| [http://www.disease-ontology.org/?id=DOID:0080389 DOID:0080389]

|

|

|

|-

| nephrotic syndrome, type 10

| class of disease

| familial nephrotic syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080386 DOID:0080386]

|

|

|

|-

| nephrotic syndrome, type 4

| class of disease

| nephrotic syndrome
familial nephrotic syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080383 DOID:0080383]

|

|

|

|-

| nephrotic syndrome, type 6

| class of disease

| familial nephrotic syndrome
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080384 DOID:0080384]

|

|

|

|-

| nephrotic syndrome, type 9

| class of disease

| familial nephrotic syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080391 DOID:0080391]

|

|

|

|-

| nerve compression syndrome

| class of disease

| peripheral neuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:573 DOID:573]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.550 C10.668.829.550]

| Nerve compression syndromes

|

|-

| nerve fibre bundle defect

| class of disease

| visual pathway disease
retinal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5678 DOID:5678]

|

|

|

|-

| nerve plexus neoplasm

| class of disease

| peripheral nervous system neoplasm
plexopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4693 DOID:4693]

|

|

|

|-

| nerve root neoplasm

| class of disease

| peripheral nervous system neoplasm
radiculopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4698 DOID:4698]

|

|

|

|-

| nerve sheath neoplasms

| class of disease

| peripheral nervous system neoplasm
neoplasm

| peripheral nervous system neoplasm that is located in the connective tissue surrounding nerves

| [http://www.disease-ontology.org/?id=DOID:3193 DOID:3193]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.600 C04.557.580.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.551.775.500 C10.551.775.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.725.500 C10.668.829.725.500]

|

|

|-

| nervous system benign neoplasm

| class of disease

| organ system benign neoplasm
neurological disorder
nervous system neoplasm

| organ system benign neoplasm that is located in the central nervous system or located in the peripheral nervous system

| [http://www.disease-ontology.org/?id=DOID:0060115 DOID:0060115]

|

|

|

|-

| nervous system cancer

| class of disease

| organ system cancer
nervous system neoplasm
neurological disorder

| organ system cancer located in the nervous system that affects the central or peripheral nervous system

| [http://www.disease-ontology.org/?id=DOID:3093 DOID:3093]

|

| Nervous system neoplasms

|

|-

| nervous system hibernoma

| class of disease

| nervous system cancer
hibernoma
central nervous system lipoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6607 DOID:6607]

|

|

|

|-

| nervous system malformations

| class of disease

| congenital disorder
central nervous system disease
neurological disorder
disease

| congenital conditions that stem from damage to, or abnormal development of, the budding nervous system

| [http://www.disease-ontology.org/?id=DOID:2490 DOID:2490]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.500 C10.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.666 C16.131.666]

| Congenital diseases and disorders of the nervous system

|

|-

| nested variant infiltrating bladder urothelial carcinoma

| class of disease

| invasive bladder transitional cell carcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:7969 DOID:7969]

|

|

|

|-

| neurilemmoma

| class of disease

| neuroma
disease

| benign tumor of the nerve sheat composed of Schwann cells

| [http://www.disease-ontology.org/?id=DOID:3192 DOID:3192]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.650.595 C04.557.465.625.650.595]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.600.610.595 C04.557.580.600.610.595]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.650.595 C04.557.580.625.650.595]

| Schwannoma

| File:Peripheral schwannoma Antoni type A (1).JPG

|-

| neurilemmoma of the fifth cranial nerve

| class of disease

| trigeminal nerve neoplasm
neurilemmoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3202 DOID:3202]

|

|

|

|-

| neurilemmoma of the pleura

| class of disease

| peripheral nerve schwannoma
pleural disease
respiratory system benign neoplasm
rare respiratory disease
benign neoplasm of pleura

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6564 DOID:6564]

|

|

|

|-

| neuritis

| class of disease
symptom or sign

| peripheral neuropathy
inflammation
disease

| inflammation of a nerve or the general inflammation of the peripheral nervous system

| [http://www.disease-ontology.org/?id=DOID:1803 DOID:1803]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.650 C10.668.829.650]

| Neuritis

|

|-

| neuroaxonal dystrophy

| class of disease

| cerebral degeneration

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2367 DOID:2367]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.744 C10.228.140.744]

|

|

|-

| neurobehavioral disorder with prenatal alcohol exposure

| class of disease

| fetal alcohol spectrum disorders

| human disease

| [http://www.disease-ontology.org/?id=DOID:0081052 DOID:0081052]

|

|

|

|-

| neuroblastoma

| class of disease
cancer

| autonomic nervous system neoplasm
neuroblastic tumor
disease
childhood cancer

| autonomic nervous system neoplasm derived from immature nerve cells

| [http://www.disease-ontology.org/?id=DOID:769 DOID:769]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.600.590.650.550 C04.557.465.625.600.590.650.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.670.590.650.550 C04.557.470.670.590.650.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.600.590.650.550 C04.557.580.625.600.590.650.550]

| Neuroblastoma

| File:Neuroblastoma rosettes.jpg

|-

| neurocirculatory asthenia

| class of disease

| somatoform disorder

| somatoform disorder that involves heart disease symptoms without any identifiable physiological abnormatlities.

| [http://www.disease-ontology.org/?id=DOID:11569 DOID:11569]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.080.500 F03.080.500]

|

|

|-

| neurodegeneration

| class of disease

| central nervous system disease
degenerative disease
disease

| central nervous system disease

| [http://www.disease-ontology.org/?id=DOID:1289 DOID:1289]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574 C10.574]

| Neurodegenerative diseases and disorders

| File:Parasagittal MRI of human head in patient with benign familial macrocephaly prior to brain injury (ANIMATED).gif

|-

| neurodegeneration with brain iron accumulation

| class of disease

| iron metabolism disease
neurodegeneration
genetic neurodegenerative disease with dementia
neuroaxonal dystrophy
neurometabolic disease
metabolic disease with dementia
miscellaneous movement disorder due to genetic neurodegenerative disease

| neurodegenerative disease characterized by progressive iron accumulation in the basal ganglia and other regions of the brain, resulting in extrapyramidal movements, such as parkinsonism and dystonia

| [http://www.disease-ontology.org/?id=DOID:0110734 DOID:0110734]

|

|

|

|-

| neurodegeneration with brain iron accumulation 2A

| class of disease

| neurodegeneration with brain iron accumulation
genetic disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110735 DOID:0110735]

|

|

|

|-

| neurodegeneration with brain iron accumulation 2B

| class of disease

| neurodegeneration with brain iron accumulation
Infantile neuroaxonal dystrophy
genetic disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110736 DOID:0110736]

|

|

|

|-

| neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures

| class of disease

| nervous system heredodegenerative disease
neurodegeneration
autosomal recessive disease

| hereditary disease in humans

| [http://www.disease-ontology.org/?id=DOID:0070352 DOID:0070352]

|

|

|

|-

| neurodermatitis

| class of disease
symptom or sign

| dermatitis
lichen disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3309 DOID:3309]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.174.660 C17.800.174.660]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.815.660 C17.800.815.660]

| Lichen simplex chronicus

| File:Lichen simplex chronicus 1.jpg

|-

| neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies

| class of disease

| syndrome
neurodevelopmental disorder

| human disease

| [http://www.disease-ontology.org/?id=DOID:0070346 DOID:0070346]

|

|

|

|-

| neurodevelopmental disorder with midbrain and hindbrain malformations

| class of disease

| syndromic intellectual disability
genetic disease
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080312 DOID:0080312]

|

|

|

|-

| neuroectodermal tumor

| class of disease

| tumor
nervous system cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:171 DOID:171]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625 C04.557.465.625]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625 C04.557.580.625]

|

|

|-

| neuroendocrine carcinoma

| class of disease

| carcinoma
neuroendocrine tumor

| carcinoma that derives from neuroendocrine cells

| [http://www.disease-ontology.org/?id=DOID:1800 DOID:1800]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.650.240 C04.557.465.625.650.240]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.370 C04.557.470.200.025.370]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.650.240 C04.557.580.625.650.240]

|

| File:Large cell neuroendocrine carcinoma Case 120 (4387600323).jpg

|-

| neuroendocrine tumor

| class of disease

| endocrine gland cancer
rare disease
disease

| endocrine gland cancer that has material basis in neuroendocrine cells

| [http://www.disease-ontology.org/?id=DOID:169 DOID:169]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.650 C04.557.465.625.650]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.650 C04.557.580.625.650]

| Neuroendocrine tumors

|

|-

| neurofibroma

| class of disease

| nerve sheath neoplasms

| Human disease

| [http://www.disease-ontology.org/?id=DOID:962 DOID:962]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.600.580 C04.557.580.600.580]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.551.775.500.750 C10.551.775.500.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.725.500.600 C10.668.829.725.500.600]

| Neurofibroma

| File:Neurofibroma (1).jpg

|-

| neurofibroma of gallbladder

| class of disease

| neurofibroma
gallbladder cancer
malignant peripheral nerve neoplasm
liver cancer
endocrine gland cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5150 DOID:5150]

|

|

|

|-

| neurofibroma of spinal cord

| class of disease

| neurofibroma
Spinal cord cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:13742 DOID:13742]

|

|

|

|-

| neurofibroma of the esophagus

| class of disease

| gastrointestinal system disease
gastrointestinal system cancer
esophageal cancer
neurofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:961 DOID:961]

|

|

|

|-

| neurofibroma of the heart

| class of disease

| malignant peripheral nerve neoplasm
neurofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9300 DOID:9300]

|

|

|

|-

| neurofibromatosis type I

| class of disease

| neurofibromatoses
neuro-cardio-facial-cutaneous syndromes
disease

| type of neurofibromatosis disease

| [http://www.disease-ontology.org/?id=DOID:0111253 DOID:0111253]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.600.580.590.650 C04.557.580.600.580.590.650]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.700.645.650 C04.700.645.650]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.562.600.500 C10.562.600.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.500.549.400 C10.574.500.549.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.675 C10.668.829.675]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.400.560.400 C16.320.400.560.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.700.645.650 C16.320.700.645.650]

| Neurofibromatosis type 1

| File:Early neurofibromatosis.jpg

|-

| neurofibromatosis-Noonan syndrome

| class of disease

| syndrome
autosomal dominant disease
Noonan syndrome and Noonan-related syndrome
neurofibromatosis type I

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111683 DOID:0111683]

|

|

|

|-

| neurofibrosarcoma

| class of disease

| neurofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3512 DOID:3512]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.590.350.590 C04.557.450.565.590.350.590]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.350.590 C04.557.450.795.350.590]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.600.580.795 C04.557.580.600.580.795]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.551.775.500.750.750 C10.551.775.500.750.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.725.500.600.600 C10.668.829.725.500.600.600]

|

|

|-

| neurogenic arthropathy

| class of disease

| arthropathy
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14286 DOID:14286]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.550.186 C05.550.186]

| Neuropathic arthropathy

|

|-

| neurogenic bladder

| class of disease

| bladder disease
urination disorder
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12143 DOID:12143]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.900 C10.597.900]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.200.777.829.839 C12.200.777.829.839]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.968.829.760 C12.050.351.968.829.760]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.900 C23.888.592.900]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.950.829.760C C12.950.829.760C]

| Neurogenic bladder dysfunction

|

|-

| neurogenic bowel

| class of disease

| intestinal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13419 DOID:13419]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.158.272.804 C06.405.469.158.272.804]

|

|

|-

| neurological disorder

| class of disease

| disease of anatomical entity
disease

| disease of an anatomical entity located in the central or peripheral nervous system

| [http://www.disease-ontology.org/?id=DOID:0060052 DOID:0060052]
[http://www.disease-ontology.org/?id=DOID:863 DOID:863]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10 C10]

| Diseases and disorders of the nervous system

| File:Pyramidal hippocampal neuron 40x.jpg

|-

| neuroma

| class of disease

| nervous system benign neoplasm
peripheral nervous system neoplasm
tumor

| nervous system benign neoplasm that is characterized as a nerve tissue tumor

| [http://www.disease-ontology.org/?id=DOID:2001 DOID:2001]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.600.610 C04.557.580.600.610]

| Neuroma

|

|-

| neuromuscular disease

| class of disease

| peripheral neuropathy
musculoskeletal disorder
disease

| neuropathy that affect the nerves that control the voluntary muscles

| [http://www.disease-ontology.org/?id=DOID:440 DOID:440]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668 C10.668]

| Neuromuscular diseases

|

|-

| neuromuscular junction disease

| class of disease

| neuromuscular disease

| neuromuscular disease that is characterized by the disfunction of conduction through the neuromuscular junction

| [http://www.disease-ontology.org/?id=DOID:439 DOID:439]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.758 C10.668.758]

|

|

|-

| neuronal ceroid lipofuscinosis

| class of disease

| lipid storage disease
eye degenerative disease
nervous system heredodegenerative disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14503 DOID:14503]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.500.550 C10.574.500.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.400.600 C16.320.400.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.398.641.509 C16.320.565.398.641.509]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.584.563.641.509 C18.452.584.563.641.509]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.398.641.509 C18.452.648.398.641.509]

|

|

|-

| neuronal ceroid lipofuscinosis 1

| class of disease

| neuronal ceroid lipofuscinosis
Infantile neuronal ceroid lipofuscinosis
Jansky–Bielschowsky disease
juvenile neuronal ceroid lipofuscinosis
adult neuronal ceroid lipofuscinosis
genetic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110721 DOID:0110721]

|

|

|

|-

| neuronal ceroid lipofuscinosis 10

| class of disease

| neuronal ceroid lipofuscinosis
juvenile neuronal ceroid lipofuscinosis
Jansky–Bielschowsky disease
adult neuronal ceroid lipofuscinosis
congenital neuronal ceroid lipofuscinosis
genetic disease

| neuronal ceroid lipofuscinosis that has material basis in homozygous or compound heterozygous mutation in the CTSD gene on chromosome 11p15

| [http://www.disease-ontology.org/?id=DOID:0110725 DOID:0110725]

|

|

|

|-

| neuronal ceroid lipofuscinosis 2

| class of disease

| neuronal ceroid lipofuscinosis
juvenile neuronal ceroid lipofuscinosis
Jansky–Bielschowsky disease
genetic disease

| A condition associated with mutation(s) in the TPP1 gene, encoding tripeptidyl-peptidase- 1. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments.

| [http://www.disease-ontology.org/?id=DOID:0110726 DOID:0110726]

|

|

|

|-

| neuronal ceroid lipofuscinosis 3

| class of disease

| neuronal ceroid lipofuscinosis
juvenile neuronal ceroid lipofuscinosis
genetic disease

| A condition associated with mutation(s) in the CLN3 gene, encoding battenin. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments.

| [http://www.disease-ontology.org/?id=DOID:0110731 DOID:0110731]

|

|

|

|-

| neuronal ceroid lipofuscinosis 4A

| class of disease

| neuronal ceroid lipofuscinosis
adult neuronal ceroid lipofuscinosis
genetic disease
Kufs disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110730 DOID:0110730]

|

|

|

|-

| neuronal ceroid lipofuscinosis 5

| class of disease

| neuronal ceroid lipofuscinosis
Jansky–Bielschowsky disease
genetic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110728 DOID:0110728]

|

|

|

|-

| neuronal ceroid lipofuscinosis 6

| class of disease

| neuronal ceroid lipofuscinosis
Jansky–Bielschowsky disease
adult neuronal ceroid lipofuscinosis
genetic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110729 DOID:0110729]

|

|

|

|-

| neuronal ceroid lipofuscinosis 7

| class of disease

| neuronal ceroid lipofuscinosis
Jansky–Bielschowsky disease
genetic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110722 DOID:0110722]

|

|

|

|-

| neuronal ceroid lipofuscinosis 8

| class of disease

| neuronal ceroid lipofuscinosis
Jansky–Bielschowsky disease
juvenile neuronal ceroid lipofuscinosis
genetic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0110723 DOID:0110723]

|

|

|

|-

| neuronal ceroid lipofuscinosis 9

| class of disease

| neuronal ceroid lipofuscinosis
juvenile neuronal ceroid lipofuscinosis

| neuronal ceroid lipofuscinosis that is characterized by juvenile-onset of progressive vision loss, progressive ataxia and seziures

| [http://www.disease-ontology.org/?id=DOID:0110733 DOID:0110733]

|

|

|

|-

| neuronal intestinal dysplasia

| class of disease

| colonic disease
intestinal pseudo-obstruction
intestinal dysganglionosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0080072 DOID:0080072]

|

|

|

|-

| neuronal intestinal dysplasia type A

| class of disease

| neuronal intestinal dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080679 DOID:0080679]

|

|

|

|-

| neuronal intestinal dysplasia type B

| class of disease

| neuronal intestinal dysplasia

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080680 DOID:0080680]

|

|

|

|-

| neuronitis

| class of disease

| central nervous system disease
neurological disorder
inflammatory disease
disease

| central nervous system disease that is characterized by neuron inflammation

| [http://www.disease-ontology.org/?id=DOID:8117 DOID:8117]

|

|

|

|-

| neuronopathy, distal hereditary motor, type 5B

| class of disease

| nervous system heredodegenerative disease
distal hereditary motor neuronopathy type 5

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111205 DOID:0111205]

|

|

|

|-

| neurooculocardiogenitourinary syndrome

| class of disease

| syndrome
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111675 DOID:0111675]

|

|

|

|-

| neuropathy

| class of disease

| neurological disorder

| disease of or damage to the nerves

| [http://www.disease-ontology.org/?id=DOID:870 DOID:870]

|

| Neuropathies

|

|-

| neuroretinitis

| class of disease

| optic papillitis
focal chorioretinitis
eye disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10176 DOID:10176]

|

|

|

|-

| neurosarcoidosis

| class of disease

| sarcoidosis
central nervous system disease

| disease with granulomas invoving nervous tissue

| [http://www.disease-ontology.org/?id=DOID:13403 DOID:13403]

|

| Neurosarcoidosis

|

|-

| neurotrophic keratoconjunctivitis

| class of disease

| keratoconjunctivitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12125 DOID:12125]

|

|

|

|-

| neutropenia

| class of disease

| agranulocytosis
disease

| abnormally low concentration of neutrophils in the blood

| [http://www.disease-ontology.org/?id=DOID:1227 DOID:1227]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.553.546.184.564 C15.378.553.546.184.564]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.243.750.184.564 C15.378.243.750.184.564]

| Neutropenia

| File:Neutropenia.JPG

|-

| nevoid basal cell carcinoma syndrome

| class of disease
symptom or sign

| autosomal dominant disease
syndrome

| an autosomal dominant condition that can cause unusual facial appearances and a predisposition for basal-cell carcinoma

| [http://www.disease-ontology.org/?id=DOID:2512 DOID:2512]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.182.089.530.690.150 C04.182.089.530.690.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.165.150 C04.557.470.200.165.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.565.165.150 C04.557.470.565.165.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.700.175 C04.700.175]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.099.105 C05.116.099.105]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.500.470.690.150 C05.500.470.690.150]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.320.450.670.130 C07.320.450.670.130]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.077.130 C16.131.077.130]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.700.175 C16.320.700.175]

|

|

|-

| nickel allergic asthma

| class of disease

| allergic asthma
nickel sensitivity
metal allergy

| allergic asthma that has allergic trigger nickel atom

| [http://www.disease-ontology.org/?id=DOID:0040045 DOID:0040045]

|

|

|

|-

| night blindness

| class of disease

| eye disease
retinal disease
vision disorder
disease

| condition making it difficult or impossible to see in relatively low light

| [http://www.disease-ontology.org/?id=DOID:8499 DOID:8499]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.966.671 C11.966.671]

| Nyctalopia

| File:P360 Onderdendam goed nachtzicht ns nachtblind.jpg

|-

| nipple carcinoma

| class of disease

| breast carcinoma
malignant neoplasm of nipple

| breast carcinoma that is located in the nipple

| [http://www.disease-ontology.org/?id=DOID:6629 DOID:6629]

|

|

|

|-

| nipple duct carcinoma

| class of disease

| nipple carcinoma

| nipple carcinoma that is located in the nipple duct

| [http://www.disease-ontology.org/?id=DOID:7953 DOID:7953]

|

|

|

|-

| nipple neoplasm

| class of disease

| breast benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3003 DOID:3003]

|

|

|

|-

| nocturnal asthma

| class of disease

| chronic asthma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080826 DOID:0080826]

|

|

|

|-

| nodal marginal zone B cell lymphoma

| class of disease

| marginal zone B-cell lymphoma

| marginal zone B-cell lymphoma which morphologically resembles lymph nodes involved by marginal zone lymphomas of extranodal or splenic types, but without evidence of extranodal or splenic disease

| [http://www.disease-ontology.org/?id=DOID:0080211 DOID:0080211]

|

|

|

|-

| nodular basal cell carcinoma

| class of disease

| basal-cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4280 DOID:4280]

|

|

|

|-

| nodular degeneration of cornea

| class of disease

| corneal degeneration

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2879 DOID:2879]

|

|

|

|-

| nodular episcleritis

| class of disease

| scleral disease
episcleritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:728 DOID:728]

|

|

|

|-

| nodular ganglioneuroblastoma

| class of disease

| ganglioneuroblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5193 DOID:5193]

|

|

|

|-

| nodular goiter

| class of disease

| goiter

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13197 DOID:13197]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.874.283.501 C19.874.283.501]

|

|

|-

| nodular hidradenoma

| class of disease

| hidradenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2061 DOID:2061]

|

|

|

|-

| nodular medulloblastoma

| class of disease

| medulloblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3873 DOID:3873]

|

|

|

|-

| nodular melanoma

| class of disease

| skin melanoma

| melanoma that is characterized as highly aggressive and manifests as a uniform blue-black, blue-red, or amelanotic nodule

| [http://www.disease-ontology.org/?id=DOID:10047 DOID:10047]

|

| Nodular melanoma

|

|-

| nodular nonsuppurative panniculitis

| class of disease

| panniculitis
subcutaneous tissue disease

| cutaneous condition characterized by recurrent subcutaneous nodules that heal with depression of the overlying skin

| [http://www.disease-ontology.org/?id=DOID:1525 DOID:1525]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.710.500 C17.300.710.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.566.500 C17.800.566.500]

|

|

|-

| nodular prostate

| class of disease

| prostatic hypertrophy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13206 DOID:13206]

|

|

|

|-

| nodular tenosynovitis

| class of disease

| connective tissue benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2701 DOID:2701]

|

|

|

|-

| non specific chronic endometritis

| class of disease

| endometritis
chronic endometritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4560 DOID:4560]

|

|

|

|-

| non-Hodgkin lymphoma

| class of disease

| lymphoma
neoplasm
hematopoietic system disease
disease

| type of cancer of lymph nodes

| [http://www.disease-ontology.org/?id=DOID:0060060 DOID:0060060]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.386.480 C04.557.386.480]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.515.569.480 C15.604.515.569.480]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.683.515.761.480 C20.683.515.761.480]

| Non-Hodgkin lymphomas

| File:Mantle cell lymphoma - intermed mag.jpg

|-

| non-Langerhans-cell histiocytosis

| class of disease

| histiocytosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4330 DOID:4330]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.604.250.410 C15.604.250.410]

|

|

|-

| non-alcoholic fatty liver

| class of disease

| non-alcoholic fatty liver disease

| nonalcoholic fatty liver disease that is characterized by the presence of at least 5% of hepatic steatosis with no evidence of hepatocellular injury in the form of hepatocyte ballooning

| [http://www.disease-ontology.org/?id=DOID:0080546 DOID:0080546]

|

|

|

|-

| non-alcoholic fatty liver disease

| class of disease

| fatty liver disease
disease

| storing of excess fat in liver cells, not caused by heavy alcohol use

| [http://www.disease-ontology.org/?id=DOID:0080208 DOID:0080208]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.241.519 C06.552.241.519]

|

|

|-

| non-alcoholic steatohepatitis

| class of disease

| non-alcoholic fatty liver disease

| Fatty replacement and damage to the hepatocytes not related to alcohol use. It may lead to cirrhosis and liver failure.

| [http://www.disease-ontology.org/?id=DOID:0080547 DOID:0080547]

|

|

|

|-

| non-arteritic anterior ischemic optic neuropathy

| class of disease

| anterior ischemic optic neuropathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050864 DOID:0050864]

|

|

|

|-

| non-congenital cyst of kidney

| class of disease

| cystic kidney disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9621 DOID:9621]

|

|

|

|-

| non-controlled substance abuse

| class of disease

| addiction
substance use disorder
social issue

| abuse of chemical substances and/or abuse of any licit substances

| [http://www.disease-ontology.org/?id=DOID:9973 DOID:9973]

|

| Substance dependence

| File:Toxicoman - Substance abuse.jpg

|-

| non-functioning pancreatic endocrine tumor

| class of disease

| islet cell tumor
non-functioning endocrine neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7698 DOID:7698]

|

|

|

|-

| non-gestational choriocarcinoma

| class of disease

| choriocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4320 DOID:4320]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.955.207.438 C04.557.465.955.207.438]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.455.750 C04.557.470.200.025.455.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.850.908.208.438 C04.850.908.208.438]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.720.949.208.438 C13.703.720.949.208.438]

|

|

|-

| non-gestational ovarian choriocarcinoma

| class of disease

| ovarian primitive germ cell tumor
choriocarcinoma of ovary

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7665 DOID:7665]

|

|

|

|-

| non-invasive bladder urothelial carcinoma

| class of disease

| bladder urothelial carcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:6571 DOID:6571]

|

|

|

|-

| non-proliferative fibrocystic change of the breast

| class of disease

| breast fibrocystic disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5997 DOID:5997]

|

|

|

|-

| non-renal secondary hyperparathyroidism

| class of disease

| hyperparathyroidism
secondary hyperparathyroidism

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13575 DOID:13575]

|

|

|

|-

| non-secretory myeloma

| class of disease

| multiple myeloma
non-functioning endocrine neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9547 DOID:9547]

|

|

|

|-

| non-small-cell lung carcinoma

| class of disease

| lung carcinoma
lung cancer
disease

| any type of epithelial lung cancer other than small-cell lung carcinoma

| [http://www.disease-ontology.org/?id=DOID:3908 DOID:3908]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.894.797.520.109.220.249 C04.588.894.797.520.109.220.249]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.540.140.500 C08.381.540.140.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.785.520.100.220.500 C08.785.520.100.220.500]

| Non-small cell lung cancer

|

|-

| non-suppurative otitis media

| class of disease

| otitis media

| otitis media which involves transudation of fluid in the middle ear without pus formation

| [http://www.disease-ontology.org/?id=DOID:11180 DOID:11180]

|

|

|

|-

| non-syndromic X-linked intellectual disability 1

| class of disease

| X-linked dominant disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112038 DOID:0112038]

|

|

|

|-

| non-syndromic X-linked intellectual disability 100

| class of disease

| non-syndromic X-linked intellectual disability
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112040 DOID:0112040]

|

|

|

|-

| non-syndromic X-linked intellectual disability 101

| class of disease

| non-syndromic X-linked intellectual disability
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112048 DOID:0112048]

|

|

|

|-

| non-syndromic X-linked intellectual disability 103

| class of disease

| X-linked recessive disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112020 DOID:0112020]

|

|

|

|-

| non-syndromic X-linked intellectual disability 104

| class of disease

| non-syndromic X-linked intellectual disability
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112018 DOID:0112018]

|

|

|

|-

| non-syndromic X-linked intellectual disability 105

| class of disease

| X-linked recessive disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112036 DOID:0112036]

|

|

|

|-

| non-syndromic X-linked intellectual disability 107

| class of disease

| X-linked dominant disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112054 DOID:0112054]

|

|

|

|-

| non-syndromic X-linked intellectual disability 14

| class of disease

| non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112027 DOID:0112027]

|

|

|

|-

| non-syndromic X-linked intellectual disability 19

| class of disease

| non-syndromic X-linked intellectual disability
X-linked dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112019 DOID:0112019]

|

|

|

|-

| non-syndromic X-linked intellectual disability 2

| class of disease

| X-linked dominant disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112016 DOID:0112016]

|

|

|

|-

| non-syndromic X-linked intellectual disability 20

| class of disease

| non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112023 DOID:0112023]

|

|

|

|-

| non-syndromic X-linked intellectual disability 21

| class of disease

| X-linked recessive disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112022 DOID:0112022]

|

|

|

|-

| non-syndromic X-linked intellectual disability 23

| class of disease

| non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112049 DOID:0112049]

|

|

|

|-

| non-syndromic X-linked intellectual disability 30

| class of disease

| non-syndromic X-linked intellectual disability
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112051 DOID:0112051]

|

|

|

|-

| non-syndromic X-linked intellectual disability 41

| class of disease

| X-linked dominant disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112058 DOID:0112058]

|

|

|

|-

| non-syndromic X-linked intellectual disability 42

| class of disease

| non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112057 DOID:0112057]

|

|

|

|-

| non-syndromic X-linked intellectual disability 45

| class of disease

| non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112028 DOID:0112028]

|

|

|

|-

| non-syndromic X-linked intellectual disability 46

| class of disease

| X-linked recessive disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112055 DOID:0112055]

|

|

|

|-

| non-syndromic X-linked intellectual disability 50

| class of disease

| non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112029 DOID:0112029]

|

|

|

|-

| non-syndromic X-linked intellectual disability 53

| class of disease

| X-linked recessive disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112047 DOID:0112047]

|

|

|

|-

| non-syndromic X-linked intellectual disability 58

| class of disease

| X-linked recessive disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112024 DOID:0112024]

|

|

|

|-

| non-syndromic X-linked intellectual disability 63

| class of disease

| non-syndromic X-linked intellectual disability
X-linked dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112050 DOID:0112050]

|

|

|

|-

| non-syndromic X-linked intellectual disability 72

| class of disease

| non-syndromic X-linked intellectual disability
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112059 DOID:0112059]

|

|

|

|-

| non-syndromic X-linked intellectual disability 73

| class of disease

| non-syndromic X-linked intellectual disability
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112017 DOID:0112017]

|

|

|

|-

| non-syndromic X-linked intellectual disability 77

| class of disease

| X-linked recessive disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112039 DOID:0112039]

|

|

|

|-

| non-syndromic X-linked intellectual disability 81

| class of disease

| non-syndromic X-linked intellectual disability
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112033 DOID:0112033]

|

|

|

|-

| non-syndromic X-linked intellectual disability 82

| class of disease

| non-syndromic X-linked intellectual disability
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112052 DOID:0112052]

|

|

|

|-

| non-syndromic X-linked intellectual disability 84

| class of disease

| non-syndromic X-linked intellectual disability
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112030 DOID:0112030]

|

|

|

|-

| non-syndromic X-linked intellectual disability 88

| class of disease

| non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112053 DOID:0112053]

|

|

|

|-

| non-syndromic X-linked intellectual disability 89

| class of disease

| X-linked dominant disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112031 DOID:0112031]

|

|

|

|-

| non-syndromic X-linked intellectual disability 9

| class of disease

| non-syndromic X-linked intellectual disability
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112034 DOID:0112034]

|

|

|

|-

| non-syndromic X-linked intellectual disability 90

| class of disease

| X-linked recessive disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112041 DOID:0112041]

|

|

|

|-

| non-syndromic X-linked intellectual disability 91

| class of disease

| non-syndromic X-linked intellectual disability
X-linked dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112043 DOID:0112043]

|

|

|

|-

| non-syndromic X-linked intellectual disability 92

| class of disease

| X-linked recessive disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112032 DOID:0112032]

|

|

|

|-

| non-syndromic X-linked intellectual disability 93

| class of disease

| X-linked recessive disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112045 DOID:0112045]

|

|

|

|-

| non-syndromic X-linked intellectual disability 96

| class of disease

| X-linked recessive disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112035 DOID:0112035]

|

|

|

|-

| non-syndromic X-linked intellectual disability 97

| class of disease

| non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112046 DOID:0112046]

|

|

|

|-

| non-syndromic X-linked intellectual disability 98

| class of disease

| non-syndromic X-linked intellectual disability
X-linked dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112044 DOID:0112044]

|

|

|

|-

| non-syndromic X-linked intellectual disability 99

| class of disease

| X-linked recessive disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112026 DOID:0112026]

|

|

|

|-

| non-syndromic X-linked intellectual disability ARX-related

| class of disease

| X-linked recessive disease
non-syndromic X-linked intellectual disability

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112021 DOID:0112021]

|

|

|

|-

| nonencapsulated sclerosing carcinoma

| class of disease

| papillary thyroid cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5914 DOID:5914]

|

|

|

|-

| noninfectious dermatoses of eyelid

| class of disease

| blepharitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1894 DOID:1894]

|

|

|

|-

| noninvasive malignant thymoma

| class of disease

| thymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7214 DOID:7214]

|

|

|

|-

| nonossifying fibromyxoid tumor

| class of disease

| mesenchymal cell neoplasm
fibromyxoid tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8305 DOID:8305]

|

|

|

|-

| nonphotosensitive trichothiodystrophy

| class of disease

| trichothiodystrophy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111867 DOID:0111867]

|

|

|

|-

| nonsyndromic aplasia cutis congenita

| class of disease

| skin disease
aplasia cutis congenita

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080661 DOID:0080661]

|

|

|

|-

| nonsyndromic congenital nail disorder

| class of disease

| nail disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080683 DOID:0080683]

|

|

|

|-

| nonsyndromic congenital nail disorder 1

| class of disease

| nail disease
Twenty-nail dystrophy
inherited isolated nail anomaly
epidermal disease
nonsyndromic congenital nail disorder
autosomal dominant disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0080079 DOID:0080079]

|

|

|

|-

| nonsyndromic congenital nail disorder 2

| class of disease

| nail disease
inherited isolated nail anomaly
nonsyndromic congenital nail disorder
autosomal dominant disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0080080 DOID:0080080]

|

|

|

|-

| nonsyndromic congenital nail disorder 5

| class of disease

| nail disease
inherited isolated nail anomaly
nonsyndromic congenital nail disorder
autosomal dominant disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0080083 DOID:0080083]

|

|

|

|-

| nonsyndromic congenital nail disorder 6

| class of disease

| nail disease
autosomal dominant disease
nonsyndromic congenital nail disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0080084 DOID:0080084]

|

|

|

|-

| nonsyndromic congenital nail disorder 7

| class of disease

| nail disease
epidermal disease
inherited isolated nail anomaly
nonsyndromic congenital nail disorder
autosomal dominant disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0080085 DOID:0080085]

|

|

|

|-

| nonsyndromic congenital nail disorder 9

| class of disease

| nail disease
inherited isolated nail anomaly
autosomal recessive disease
nonsyndromic congenital nail disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0080087 DOID:0080087]

|

|

|

|-

| nontoxic goiter

| class of disease

| goiter

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13195 DOID:13195]

|

|

|

|-

| normal pressure hydrocephalus

| class of disease

| communicating hydrocephalus
nervous system heredodegenerative disease
genetic dementia
disease

| condition in which there is excess cerebrospinal fluid in the ventricles, and with normal or slightly elevated cerebrospinal fluid pressure

| [http://www.disease-ontology.org/?id=DOID:1572 DOID:1572]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.602.750 C10.228.140.602.750]

| Normal pressure hydrocephalus

|

|-

| normocytic anemia

| class of disease

| anemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:720 DOID:720]

|

|

|

|-

| norwegian scabies

| class of disease

| scabies

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14374 DOID:14374]

|

| Crusted scabies

| File:Norwegian Scabies in Homeless AIDS Patient.jpg

|-

| nose disease

| class of disease

| upper respiratory tract disease
disease

| respiratory disease

| [http://www.disease-ontology.org/?id=DOID:2825 DOID:2825]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.460 C08.460]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.603 C09.603]

| Diseases and disorders of the nose and paranasal sinuses

|

|-

| notochordal cancer

| class of disease

| bone cancer

| embryonal cancer and bone cancer and mesenchymal cell neoplasm that is located in the notochord

| [http://www.disease-ontology.org/?id=DOID:3303 DOID:3303]

|

|

|

|-

| nuclear senile cataract

| class of disease

| senile cataract
nuclear sclerosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13963 DOID:13963]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency

| class of disease

| mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112065 DOID:0112065]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 1

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112074 DOID:0112074]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 10

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112075 DOID:0112075]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 11

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112089 DOID:0112089]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 12

| class of disease

| nuclear type mitochondrial complex I deficiency
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112099 DOID:0112099]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 13

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112076 DOID:0112076]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 14

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112094 DOID:0112094]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 15

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112077 DOID:0112077]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 16

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112096 DOID:0112096]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 17

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112078 DOID:0112078]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 18

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112070 DOID:0112070]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 19

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112085 DOID:0112085]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 2

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112083 DOID:0112083]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 20

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112072 DOID:0112072]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 21

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112088 DOID:0112088]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 22

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112069 DOID:0112069]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 23

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112087 DOID:0112087]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 24

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112079 DOID:0112079]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 25

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112067 DOID:0112067]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 26

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112086 DOID:0112086]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 27

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112090 DOID:0112090]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 28

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112095 DOID:0112095]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 29

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112084 DOID:0112084]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 3

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112093 DOID:0112093]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 30

| class of disease

| nuclear type mitochondrial complex I deficiency
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112098 DOID:0112098]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 31

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112071 DOID:0112071]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 32

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112080 DOID:0112080]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 33

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112097 DOID:0112097]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 34

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112091 DOID:0112091]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 35

| class of disease

| autosomal recessive disease
mitochondrial complex I deficiency
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112139 DOID:0112139]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 4

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112082 DOID:0112082]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 5

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112068 DOID:0112068]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 6

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112066 DOID:0112066]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 7

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112092 DOID:0112092]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 8

| class of disease

| nuclear type mitochondrial complex I deficiency
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112081 DOID:0112081]

|

|

|

|-

| nuclear type mitochondrial complex I deficiency 9

| class of disease

| autosomal recessive disease
nuclear type mitochondrial complex I deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112073 DOID:0112073]

|

|

|

|-

| null-cell leukemia

| class of disease

| acute lymphocytic leukemia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9954 DOID:9954]

|

|

|

|-

| nutmeg liver

| class of disease

| hepatic vascular disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:13739 DOID:13739]

|

| Congestive hepatopathy

|

|-

| nutrition disorder

| class of disease

| acquired metabolic disease
nutritional and metabolic diseases
food-related disease

| disease that results from excessive or inadequate intake of food and nutrients

| [http://www.disease-ontology.org/?id=DOID:374 DOID:374]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.654 C18.654]

| Nutritional diseases and disorders

|

|-

| nutritional deficiency disease

| class of disease

| nutrition disorder
deficiency

| human disease

| [http://www.disease-ontology.org/?id=DOID:5113 DOID:5113]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.654.521.500 C18.654.521.500]

| Diseases and disorders due to nutritional deficiencies

|

|-

| nutritional optic neuropathy

| class of disease

| optic nerve disease
optic neuritis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1209 DOID:1209]

|

|

|

|-

| nystagmus, congenital, autosomal recessive

| class of disease

| congenital nystagmus
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111797 DOID:0111797]

|

|

|

|-

| obsessive-compulsive disorder

| class of disease

| anxiety disorder
impulse control disorder
genetic nervous system disorder
genetic disease
disease

| anxiety disorder that involves unwanted and repeated thoughts, feelings, ideas, sensations (obsessions), or behaviors that make them feel driven to do something (compulsions)

| [http://www.disease-ontology.org/?id=DOID:10933 DOID:10933]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.080.600 F03.080.600]

| Obsessive–compulsive disorder

| File:Obsessive-compulsive disorder world map - DALY - WHO2002.svg

|-

| obsessive-compulsive personality disorder

| class of disease

| personality disorder
disease

| personal perfectionism at the cost of flexibility, openness, efficiency & effect on others

| [http://www.disease-ontology.org/?id=DOID:10932 DOID:10932]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.675.150 F03.675.150]

| Obsessive compulsive personality disorder

|

|-

| obstructive hydrocephalus

| class of disease

| hydrocephalus

| abnormal accumulation of cerebrospinal fluid within the ventricles of the brain that occurs as a consequence of an obstruction at any location within the ventricular system that prevents cerebrospinal fluid flowing into the subarachnoid space

| [http://www.disease-ontology.org/?id=DOID:14159 DOID:14159]

|

|

|

|-

| obstructive jaundice

| class of disease

| cholestasis
jaundice
non-neoplastic bile duct disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13603 DOID:13603]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.429.500.755 C23.550.429.500.755]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.885.375.500 C23.888.885.375.500]

| Obstructive jaundice

|

|-

| obstructive lung disease

| class of disease

| lung disease
disease

| category of respiratory disease characterized by airway obstruction

| [http://www.disease-ontology.org/?id=DOID:2320 DOID:2320]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.381.495 C08.381.495]

|

|

|-

| obstructive nephropathy

| class of disease

| kidney disease

| kidney disease characterized by kidney damage and dysfunction resulting from urinary tract obstruction

| [http://www.disease-ontology.org/?id=DOID:0070314 DOID:0070314]

|

|

|

|-

| obstructive sleep apnea

| class of disease

| sleep apnea

| obstruction of the upper airway during sleep

| [http://www.disease-ontology.org/?id=DOID:0050848 DOID:0050848]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.618.085.852.850 C08.618.085.852.850]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.886.425.800.750.850 C10.886.425.800.750.850]

|

|

|-

| occipital lobe neoplasm

| class of disease

| cerebrum cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:910 DOID:910]

|

|

|

|-

| occlusion of gallbladder

| class of disease

| gallbladder disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9714 DOID:9714]

|

|

|

|-

| occlusion precerebral artery

| class of disease

| cerebrovascular disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:5976 DOID:5976]

|

|

|

|-

| occupational asthma

| class of disease

| occupational disease
asthma
environmental induced asthma

| medical condition caused or exacerbated by the workplace

| [http://www.disease-ontology.org/?id=DOID:0080820 DOID:0080820]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.127.108.495 C08.127.108.495]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.674.095.495 C08.674.095.495]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.680.095.495 C20.543.480.680.095.495]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C24.102 C24.102]

|

|

|-

| occupational dermatitis

| class of disease

| contact dermatitis
occupational disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4404 DOID:4404]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.174.255.700 C17.800.174.255.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.815.255.700 C17.800.815.255.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C24.270 C24.270]

|

|

|-

| ochronosis

| class of disease

| connective tissue disease
clinical sign
disease

| syndrome caused by the accumulation of homogentisic acid in connective tissues

| [http://www.disease-ontology.org/?id=DOID:14223 DOID:14223]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.744 C23.550.744]

| Ochronosis

| File:Homogentisic acid.svg

|-

| ocular albinism

| class of disease

| eye disease
albinism
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050633 DOID:0050633]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.270.040.090 C11.270.040.090]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.290.040.090 C16.320.290.040.090]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.565.100.102.090 C16.320.565.100.102.090]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.850.080.090 C16.320.850.080.090]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.621.440.102.090 C17.800.621.440.102.090]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.827.080.090 C17.800.827.080.090]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.648.100.102.090 C18.452.648.100.102.090]

|

|

|-

| ocular albinism type 2

| class of disease

| ocular albinism
eye disease
X-linked recessive disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050630 DOID:0050630]

|

|

|

|-

| ocular albinism with sensorineural deafness

| class of disease

| ocular albinism
Waardenburg's syndrome
autosomal dominant disease
digenic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0090100 DOID:0090100]

|

|

|

|-

| ocular cancer

| class of disease

| sensory system cancer
eye tumor
eye disease
disease

| type of cancer un the eye

| [http://www.disease-ontology.org/?id=DOID:2174 DOID:2174]

|

|

|

|-

| ocular hyperemia

| class of disease

| conjunctival disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1248 DOID:1248]

|

|

|

|-

| ocular hypertension

| class of disease

| eye disease
hypertension
disease

| eye disease that is characterized by elevated intraocular pressure in the absence of optic nerve damage or visual field loss

| [http://www.disease-ontology.org/?id=DOID:9282 DOID:9282]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.525 C11.525]

|

|

|-

| ocular hypotension

| class of disease

| eye disease
hypotension

| Human disease

| [http://www.disease-ontology.org/?id=DOID:790 DOID:790]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.540 C11.540]

|

|

|-

| ocular motility disease

| class of disease

| cranial nerve disease
eye adnexa disease
eye disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:1279 DOID:1279]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.758 C10.228.758]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.562 C10.292.562]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.590 C11.590]

|

|

|-

| ocular tuberculosis

| class of disease

| extrapulmonary tuberculosis
eye disease
tuberculosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:233 DOID:233]
[http://www.disease-ontology.org/?id=DOID:0070344 DOID:0070344]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.289.800 C01.150.252.289.800]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.375.354.800 C01.375.354.800]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.294.354.800 C11.294.354.800]

|

|

|-

| oculocutaneous albinism type 2

| class of disease

| oculocutaneous albinism

| oculocutaneous albinism that has material basis in an autosomal recessive mutation of OCA2 on chromosome 15q12-q13

| [http://www.disease-ontology.org/?id=DOID:0070096 DOID:0070096]

|

|

|

|-

| oculocutaneous albinism type 3

| class of disease

| oculocutaneous albinism

| oculocutaneous albinism that has material basis in an autosomal recessive mutation of TYRP1 on chromosome 9p23

| [http://www.disease-ontology.org/?id=DOID:0070097 DOID:0070097]

|

|

|

|-

| oculocutaneous albinism type 4

| class of disease

| oculocutaneous albinism

| An oculocutaneous albinism that has material basis in an autosomal recessive mutation of SLC45A2 on chromosome 5p13.2.

| [http://www.disease-ontology.org/?id=DOID:0070098 DOID:0070098]

|

|

|

|-

| oculocutaneous albinism type IA

| class of disease

| oculocutaneous albinism

| An oculocutaneous albinism that has material basis in an autosomal recessive null mutation of TYR on chromosome 11q14.3 with no residual protein activity.

| [http://www.disease-ontology.org/?id=DOID:0070094 DOID:0070094]

|

|

|

|-

| oculocutaneous albinism type IB

| class of disease

| oculocutaneous albinism

| An oculocutaneous albinism that has material basis in an autosomal recessive hypomorphic mutation of TYR on chromosome 11q14.3 with retention of some residual protein activity.

| [http://www.disease-ontology.org/?id=DOID:0070095 DOID:0070095]

|

|

|

|-

| oculocutaneous albinism type V

| class of disease

| oculocutaneous albinism

| oculocutaneous albinism that has material basis in an autosomal recessive mutation of OCA5 on chromosome 4q24

| [http://www.disease-ontology.org/?id=DOID:0070099 DOID:0070099]

|

|

|

|-

| oculoglandular tularemia

| class of disease

| tularemia

| tularemia that results in inflammation of eye and swelling of lymph glands in front of the ear

| [http://www.disease-ontology.org/?id=DOID:13226 DOID:13226]

|

|

|

|-

| oculogyric crisis

| class of disease

| focal dystonia
disease

| focal dystonia that is characterized by a prolonged involuntary upward deviation of the eyes

| [http://www.disease-ontology.org/?id=DOID:0050842 DOID:0050842]

|

|

|

|-

| oculomotor nerve paralysis

| class of disease

| third cranial nerve disease
paralytic squint

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11550 DOID:11550]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.562.700 C10.292.562.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.590.436 C11.590.436]

| Oculomotor nerve palsy

|

|-

| oculopharyngodistal myopathy 4

| class of disease

| Oculopharyngodistal myopathy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0081300 DOID:0081300]

|

|

|

|-

| odontoclasia

| class of disease

| dental caries

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11736 DOID:11736]

|

|

|

|-

| olecranon bursitis

| class of disease

| enthesopathy
bursitis
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12581 DOID:12581]

|

| Olecranon bursitis

| File:Bursitis Elbow WC.JPG

|-

| olfactory groove meningioma

| class of disease

| anterior cranial fossa meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8057 DOID:8057]

|

|

|

|-

| olfactory nerve disease

| class of disease

| glossopharyngeal nerve disease
encephalopathy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:367 DOID:367]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.650 C10.292.650]

|

|

|-

| oligoasthenoteratospermia

| class of disease

| oligospermia
Teratospermia
asthenozoospermia
male infertility

| A form of male infertility that is characterized by a combination of low number or oligozoospermia, poor motility or asthenozoospermia, and abnormal shape or teratozoospermia of sperms. OAT is the most common cause of male subfertility.

| [http://www.disease-ontology.org/?id=DOID:0070311 DOID:0070311]

|

|

|

|-

| oligodendroglioma

| class of disease

| glioma
disease

| type of glioma that are believed to originate from the oligodendrocytes of the brain or from a glial precursor cell

| [http://www.disease-ontology.org/?id=DOID:3181 DOID:3181]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.600.380.590 C04.557.465.625.600.380.590]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.670.380.590 C04.557.470.670.380.590]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.600.380.590 C04.557.580.625.600.380.590]

| Oligodendrogliomas

| File:Oligodendroglioma1 high mag.jpg

|-

| oligohydramnios

| class of disease

| placenta disease
disease

| placenta disease that is characterized by a deficiency of amniotic fluid sometimes resulting in an embryonic defect through adherence between embryo and amnion

| [http://www.disease-ontology.org/?id=DOID:12215 DOID:12215]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.703.560 C13.703.560]

| Oligohydramnios

|

|-

| oligospermia

| class of disease

| male infertility
disease

| semen with abnormally low concentration of sperm

| [http://www.disease-ontology.org/?id=DOID:14228 DOID:14228]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.365.700.508 C12.294.365.700.508]

| Oligospermia

|

|-

| olivopontocerebellar atrophy

| class of disease

| neurodegeneration

| group of sporadic and inherited neurodegenerative disorders affecting the cerebellum, pons, and inferior olives

| [http://www.disease-ontology.org/?id=DOID:14784 DOID:14784]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.177.575.550.375 C10.177.575.550.375]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.079.612.600 C10.228.140.079.612.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.252.700.650 C10.228.140.252.700.650]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.662.550.600 C10.228.662.550.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.854.787.750 C10.228.854.787.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.500.825.650 C10.574.500.825.650]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.625.600 C10.574.625.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.400.780.750 C16.320.400.780.750]

|

|

|-

| omphalocele

| class of disease

| congenital disorder
abdominal wall defect
disease

| physical disorder characterized by a defect in the development of the abdominal wall muscles, resulting in the intestines, liver and other organs to remain outside of the abdomen in a sac

| [http://www.disease-ontology.org/?id=DOID:0060327 DOID:0060327]

|

| Omphalocele

|

|-

| oncocytic breast carcinoma

| class of disease

| breast adenocarcinoma
invasive breast carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6585 DOID:6585]

|

|

|

|-

| oophoritis

| class of disease
symptom or sign

| ovarian disease
inflammatory disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:10974 DOID:10974]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.056.630.450 C13.351.500.056.630.450]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.056.750.500 C13.351.500.056.750.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.630.450 C19.391.630.450]

|

|

|-

| open-angle glaucoma

| class of disease

| glaucoma

| glaucoma characterized by optic nerve damage resulting in progressive loss of visual field and increased pressure in the eye due to trabecular blockage

| [http://www.disease-ontology.org/?id=DOID:1067 DOID:1067]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.525.381.407 C11.525.381.407]

|

|

|-

| ophthalmia neonatorum

| class of disease

| gonococcal eye infectious disease
bacterial conjunctivitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9699 DOID:9699]

|

|

|

|-

| ophthalmia nodosa

| class of disease

| eye disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9722 DOID:9722]

|

|

|

|-

| ophthalmomyiasis

| class of disease

| myiasis
eye disease
parasitic eye infection

| myiasis that involves parasitic infestation of Oestrus ovis larvae in the eye causing severe irritation, edema, and pain

| [http://www.disease-ontology.org/?id=DOID:0050268 DOID:0050268]

|

|

|

|-

| ophthalmoplegia

| class of disease
symptom or sign

| ocular motility disease
paralysis
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:539 DOID:539]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.562.750 C10.292.562.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.622.447 C10.597.622.447]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.590.472 C11.590.472]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.636.447 C23.888.592.636.447]

| Ophthalmoparesis

|

|-

| opiate dependence

| class of disease

| substance dependence
opioid use disorder

| drug dependence that involves the continued use of opiate drugs despite despite problems related to use of the substance

| [http://www.disease-ontology.org/?id=DOID:2559 DOID:2559]

|

|

|

|-

| opioid use disorder

| class of disease

| addiction
substance abuse
opioid-related disorders
disease

| substance abuse disorder that involves the recurring use of opioid drugs despite negative consequences

| [http://www.disease-ontology.org/?id=DOID:11206 DOID:11206]

|

| Opioid use disorder

|

|-

| opportunistic bacterial infectious disease

| class of disease

| bacterial infectious disease
opportunistic infection

| bacterial infectious disease that results in infection by bacteria in individuals whose host defense mechanisms have been compromised

| [http://www.disease-ontology.org/?id=DOID:0050340 DOID:0050340]

|

|

|

|-

| opportunistic mycosis

| class of disease

| systemic mycosis
opportunistic infection

| A systemic mycosis that results in fungal infection located in human body of immunocompromised individuals, has material basis in Fungi. The organisms invade via the respiratory tract, alimentary tract, or intravascular devices.

| [http://www.disease-ontology.org/?id=DOID:2473 DOID:2473]

|

|

|

|-

| oppositional defiant disorder

| class of disease

| specific developmental disorder
emotional and behavioral disorders
disease

| human disorder involving hostility and defiance

| [http://www.disease-ontology.org/?id=DOID:0050856 DOID:0050856]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.625.094.475 F03.625.094.475]

| Oppositional defiant disorder

|

|-

| optic atrophy 10

| class of disease

| autosomal dominant disease
optic atrophy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111434 DOID:0111434]

|

|

|

|-

| optic atrophy 11

| class of disease

| autosomal recessive isolated optic atrophy
autosomal recessive disease
optic atrophy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111436 DOID:0111436]

|

|

|

|-

| optic atrophy 2

| class of disease

| optic atrophy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111443 DOID:0111443]

|

|

|

|-

| optic atrophy 4

| class of disease

| Kjer's optic neuropathy
optic atrophy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111440 DOID:0111440]

|

|

|

|-

| optic atrophy 5

| class of disease

| Kjer's optic neuropathy
optic atrophy
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111438 DOID:0111438]

|

|

|

|-

| optic atrophy 6

| class of disease

| autosomal recessive isolated optic atrophy
optic atrophy
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111435 DOID:0111435]

|

|

|

|-

| optic atrophy 9

| class of disease

| autosomal recessive disease
optic atrophy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111442 DOID:0111442]

|

|

|

|-

| optic disk drusen

| class of disease

| optic nerve disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13561 DOID:13561]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.700.450 C10.292.700.450]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.640.513 C11.640.513]

|

|

|-

| optic nerve astrocytoma

| class of disease

| optic nerve glioma
optic nerve disease
astrocytoma
neuromuscular disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:4991 DOID:4991]

|

|

|

|-

| optic nerve disease

| class of disease

| cranial nerve disease
vision disorder
peripheral neuropathy
visual pathway disease
neuro-ophthalmological disease
disease

| cranial nerve disease that is located in the optic nerve

| [http://www.disease-ontology.org/?id=DOID:1891 DOID:1891]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.700 C10.292.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.640 C11.640]

| Optic neuropathy

|

|-

| optic nerve glioma

| class of disease

| optic nerve tumor
glioma
visual pathway glioma
brain glioma

| human disease

| [http://www.disease-ontology.org/?id=DOID:4992 DOID:4992]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.465.625.600.380.795 C04.557.465.625.600.380.795]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.670.380.795 C04.557.470.670.380.795]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.580.625.600.380.795 C04.557.580.625.600.380.795]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.614.300.600.600 C04.588.614.300.600.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.614.596.240.240.500 C04.588.614.596.240.240.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.225.800.500 C10.292.225.800.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.700.500.500 C10.292.700.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.551.360.500.500 C10.551.360.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.551.775.250.500.500 C10.551.775.250.500.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.640.544.500 C11.640.544.500]

|

|

|-

| optic neuritis

| class of disease

| optic nerve disease
eye disease
encephalomyelitis
disease

| optic nerve disease that results in inflammation located in optic nerve which may cause a complete or partial loss of vision

| [http://www.disease-ontology.org/?id=DOID:1210 DOID:1210]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.700.550 C10.292.700.550]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.640.576 C11.640.576]

| Optic neuritis

|

|-

| optic papillitis

| class of disease

| optic neuritis

| human disease

| [http://www.disease-ontology.org/?id=DOID:10175 DOID:10175]

|

|

|

|-

| oral cavity carcinoma in situ

| class of disease

| in situ carcinoma
mouth cancer
mouth disease
carcinoma in situ of digestive organ

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050610 DOID:0050610]

|

|

|

|-

| oral hairy leukoplakia

| class of disease

| mouth disease
oral mucosa leukoplakia
disease

| mouth disease characterized by a white patch on the lateral sides of the tongue with a corrugated or hairy appearance; caused by Epstein-Barr virus

| [http://www.disease-ontology.org/?id=DOID:0060315 DOID:0060315]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.925.256.466.313.500 C01.925.256.466.313.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.443.591.545.500 C04.588.443.591.545.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.834.512.513.500 C04.834.512.513.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.565.545.500 C07.465.565.545.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.300.816.513.500 C23.300.816.513.500]

|

|

|-

| oral leukoedema

| class of disease

| mouth disease
Leukoedema

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4557 DOID:4557]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.385 C07.465.385]

|

|

|-

| oral mucosa leukoplakia

| class of disease

| mouth disease
leukoplakia

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9655 DOID:9655]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.443.591.545 C04.588.443.591.545]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.834.512.513 C04.834.512.513]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.565.545 C07.465.565.545]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.300.816.513 C23.300.816.513]

| Oral leukoplakia

|

|-

| oral submucous fibrosis

| class of disease

| mouth disease
rare maxillo-facial surgical disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:5773 DOID:5773]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.654 C07.465.654]

|

|

|-

| oral-facial-digital syndrome

| class of disease

| syndrome

| genetic disease that is characterized by malformations of the face, oral cavity, and digits with polycystic kidney disease and variable involvement of the central nervous system and has material basis in X-linked inheritance of an OFD gene

| [http://www.disease-ontology.org/?id=DOID:4501 DOID:4501]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.099.370.652 C05.116.099.370.652]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.660.207.700 C05.660.207.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.077.676 C16.131.077.676]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.260.830.670 C16.131.260.830.670]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.131.621.207.700 C16.131.621.207.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.180.830.670 C16.320.180.830.670]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.714 C16.320.714]

|

|

|-

| orange allergy

| class of disease

| fruit allergy

| fruit allergy triggered by Citrus sinensis plant fruit food product.

| [http://www.disease-ontology.org/?id=DOID:0060508 DOID:0060508]

|

|

|

|-

| orbit embryonal rhabdomyosarcoma

| class of disease

| orbit rhabdomyosarcoma
embryonal rhabdomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3258 DOID:3258]

|

|

|

|-

| orbit rhabdomyosarcoma

| class of disease

| orbit sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3259 DOID:3259]

|

|

|

|-

| orbital cancer

| class of disease

| bone cancer
orbit neoplasm
orbital disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4143 DOID:4143]

|

|

|

|-

| orbital cyst

| class of disease

| orbital disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14233 DOID:14233]

|

|

|

|-

| orbital disease

| class of disease

| eye adnexa disease
bone disease

| adnexa disease that is located in the eye socket

| [http://www.disease-ontology.org/?id=DOID:930 DOID:930]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.675 C11.675]

|

|

|-

| orbital granuloma

| class of disease

| chronic orbital inflammation

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10499 DOID:10499]

|

|

|

|-

| orbital osteomyelitis

| class of disease

| acute orbital inflammation
osteomyelitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11232 DOID:11232]

|

|

|

|-

| orbital periostitis

| class of disease

| acute orbital inflammation

| human disease

| [http://www.disease-ontology.org/?id=DOID:11231 DOID:11231]

|

|

|

|-

| orbital tenonitis

| class of disease

| acute orbital inflammation

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11233 DOID:11233]

|

|

|

|-

| orchitis

| class of disease

| testicular disease
inflammatory disease
disease

| inflammation of the testes

| [http://www.disease-ontology.org/?id=DOID:2518 DOID:2518]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.829.493 C12.294.829.493]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.829.493 C19.391.829.493]

| Orchitis

| File:Orkite cok2 pere polets 32 samwinnes.JPG

|-

| organ system benign neoplasm

| class of disease

| benign neoplasm
disease of anatomical entity

| benign neoplasm that is classified by the organ system from which it is arising from

| [http://www.disease-ontology.org/?id=DOID:0060085 DOID:0060085]

|

|

|

|-

| organ system cancer

| class of disease

| cancer
cancer by anatomical entity

| cancer that is classified based on the organ it starts in

| [http://www.disease-ontology.org/?id=DOID:0050686 DOID:0050686]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588 C04.588]

|

|

|-

| organic acidemia

| class of disease

| amino acid metabolic disorder

| amino acid metabolic disorder that disrupts normal amino acid metabolism causing a building up of branched-chain amino acids

| [http://www.disease-ontology.org/?id=DOID:0060159 DOID:0060159]

|

|

|

|-

| orofacial cleft 1

| class of disease

| cleft lip and cleft palate
autosomal dominant disease

| An orofacial cleft characterized by autosomal dominant inheritance that has material basis in variation in chromosome region 6p24.3.

| [http://www.disease-ontology.org/?id=DOID:0080395 DOID:0080395]

|

|

|

|-

| orofacial cleft 10

| class of disease

| cleft lip and cleft palate

| orofacial cleft that has material basis in mutation in the SUMO1 gene on chromosome 2q33

| [http://www.disease-ontology.org/?id=DOID:0080403 DOID:0080403]

|

|

|

|-

| orofacial cleft 11

| class of disease

| cleft lip and cleft palate

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080404 DOID:0080404]

|

|

|

|-

| orofacial cleft 12

| class of disease

| cleft lip and cleft palate

| An orofacial cleft that has material basis in variation in the chromosome region 8q24.3.

| [http://www.disease-ontology.org/?id=DOID:0080405 DOID:0080405]

|

|

|

|-

| orofacial cleft 13

| class of disease

| cleft lip and cleft palate
autosomal dominant disease

| orofacial cleft characterized by autosomal doninant inhertitance that has material basis in variation in chromosome region 1p33 associated with enrichment of the T allele of SNP rs3827730

| [http://www.disease-ontology.org/?id=DOID:0080406 DOID:0080406]

|

|

|

|-

| orofacial cleft 14

| class of disease

| cleft lip and cleft palate
autosomal recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080407 DOID:0080407]

|

|

|

|-

| orofacial cleft 15

| class of disease

| cleft lip and cleft palate

| orofacial cleft that has material basis in mutation in the DLX4 gene on chromosome 17q21

| [http://www.disease-ontology.org/?id=DOID:0080408 DOID:0080408]

|

|

|

|-

| orofacial cleft 2

| class of disease

| cleft lip and cleft palate

| orofacial cleft that has material basis in variation in the chromosome region 2p13

| [http://www.disease-ontology.org/?id=DOID:0080396 DOID:0080396]

|

|

|

|-

| orofacial cleft 3

| class of disease

| cleft lip and cleft palate

| orofacial cleft that has material basis in variation in the chromosomal region 19q13

| [http://www.disease-ontology.org/?id=DOID:0080397 DOID:0080397]

|

|

|

|-

| orofacial cleft 4

| class of disease

| cleft lip and cleft palate

| orofacial cleft that has material basis in variation in the 4q21-q31 chromosomal region

| [http://www.disease-ontology.org/?id=DOID:0080398 DOID:0080398]

|

|

|

|-

| orofacial cleft 5

| class of disease

| cleft lip and cleft palate

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080399 DOID:0080399]

|

|

|

|-

| orofacial cleft 6

| class of disease

| autosomal dominant disease
cleft lip and cleft palate

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080593 DOID:0080593]

|

|

|

|-

| orofacial cleft 7

| class of disease

| cleft lip and cleft palate
autosomal recessive disease

| orofacial cleft that has material basis in by homozygous mutation in the PVRL1 gene on chromosome 11q23

| [http://www.disease-ontology.org/?id=DOID:0080400 DOID:0080400]

|

|

|

|-

| orofacial cleft 8

| class of disease

| cleft lip and cleft palate

| orofacial cleft that has material basis in heterozygous mutation in the TP63 gene on chromosome 3q28

| [http://www.disease-ontology.org/?id=DOID:0080401 DOID:0080401]

|

|

|

|-

| orofacial cleft 9

| class of disease

| cleft lip and cleft palate

| An orofacial cleft that has material basis in variation in the chromosome region 13q33.1-q34.

| [http://www.disease-ontology.org/?id=DOID:0080402 DOID:0080402]

|

|

|

|-

| orofaciodigital syndrome VIII

| class of disease

| oral-facial-digital syndrome
X-linked recessive disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060378 DOID:0060378]

|

|

|

|-

| oromandibular dystonia

| class of disease

| focal dystonia
lingual-facial-buccal dyskinesia
focal, segmental or multifocal dystonia

| focal dystonia that is characterized by distortions of the mouth and tongue.

| [http://www.disease-ontology.org/?id=DOID:0050843 DOID:0050843]

|

|

|

|-

| oropharyngeal anthrax

| class of disease

| gastrointestinal anthrax

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050059 DOID:0050059]

|

|

|

|-

| orthostatic proteinuria

| class of disease
symptom or sign

| kidney disease
proteinuria

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9617 DOID:9617]

|

|

|

|-

| osmotic diarrhea

| class of disease

| diarrhea
chronic diarrhea

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050130 DOID:0050130]

|

|

|

|-

| ossifying fibroma

| class of disease

| bone benign neoplasm

| bone benign neoplasm that is located in the mouth and results in an overgrowth of gingival tissue due to irritation or trauma

| [http://www.disease-ontology.org/?id=DOID:180 DOID:180]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.575.400 C04.557.450.565.575.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.590.340.360 C04.557.450.565.590.340.360]

|

|

|-

| ossifying fibromyxoid tumour

| class of disease

| fibromyxoid tumor
mesenchymal cell neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:2685 DOID:2685]

|

|

|

|-

| osteoarticular tuberculosis

| class of disease

| extrapulmonary tuberculosis
bone disease

| extrapulmonary tuberculosis that results in formation of lesions located in bone

| [http://www.disease-ontology.org/?id=DOID:1639 DOID:1639]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.252.410.040.552.846.617.525 C01.150.252.410.040.552.846.617.525]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.160.886 C01.160.886]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.165.886 C05.116.165.886]

|

|

|-

| osteoblastoma

| class of disease

| bone benign neoplasm
osteogenic neoplasm
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0060098 DOID:0060098]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.575.600 C04.557.450.565.575.600]

| Osteoblastoma

| File:Osteoblastoma - high mag.jpg

|-

| osteochondrodysplasia

| class of disease

| bone development disease

| bone development disease that results in defective development of cartilage or bone

| [http://www.disease-ontology.org/?id=DOID:2256 DOID:2256]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.099.708 C05.116.099.708]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.728 C16.320.728]

| Osteochondrodysplasias

|

|-

| osteochondrosis

| class of disease
symptom or sign

| ischemic bone disease
disease

| ischemic bone disease that results in necrosis followed by regrowth in children and teens located in bone

| [http://www.disease-ontology.org/?id=DOID:8125 DOID:8125]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.821 C05.116.821]

| Osteochondrosis

|

|-

| osteoclast-like giant cell neoplasm of the pancreas

| class of disease

| pancreatic ductal adenocarcinoma
undifferentiated pancreatic carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7718 DOID:7718]

|

|

|

|-

| osteogenesis imperfecta 21

| class of disease

| osteogenesis imperfecta

| human disease

| [http://www.disease-ontology.org/?id=DOID:0112201 DOID:0112201]

|

|

|

|-

| osteogenesis imperfecta type 1

| class of disease

| osteogenesis imperfecta
genetic disease
autosomal dominant disease

| An osteogenesis imperfecta that is characterized by bone fragility and blue sclerae and has material basis in dominantly inherited mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.

| [http://www.disease-ontology.org/?id=DOID:0110334 DOID:0110334]

|

|

|

|-

| osteogenesis imperfecta type 16

| class of disease

| osteogenesis imperfecta

| osteogenesis imperfecta that has material basis in contiguous gene deletion on chromosome 11p11

| [http://www.disease-ontology.org/?id=DOID:0110345 DOID:0110345]

|

|

|

|-

| osteogenesis imperfecta type 18

| class of disease

| autosomal recessive disease
osteogenesis imperfecta

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111848 DOID:0111848]

|

|

|

|-

| osteogenesis imperfecta type 20

| class of disease

| autosomal recessive disease
osteogenesis imperfecta

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111849 DOID:0111849]

|

|

|

|-

| osteogenesis imperfecta type 3

| class of disease

| osteogenesis imperfecta
genetic disease
autosomal dominant disease

| An osteogenesis imperfecta that is characterized by progressive limb and spinal deformity and normal sclerae and has material basis in mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.

| [http://www.disease-ontology.org/?id=DOID:0110339 DOID:0110339]

|

|

|

|-

| osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures

| class of disease

| osteogenesis imperfecta
dentinogenesis imperfecta
blue sclera

| osteogenesis imperfecta found in a single South African family

| [http://www.disease-ontology.org/?id=DOID:0110335 DOID:0110335]

|

|

|

|-

| osteomalacia

| class of disease

| bone remodeling disease
disease

| bone remodeling disease that has material basis in a vitamin D deficiency which results in softening located in bone

| [http://www.disease-ontology.org/?id=DOID:10573 DOID:10573]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.198.816.640 C05.116.198.816.640]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.104.816.640 C18.452.104.816.640]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.174.845.640 C18.452.174.845.640]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.654.521.500.133.770.734.640 C18.654.521.500.133.770.734.640]

|

| File:Calcitriol.svg

|-

| osteomyelitis

| class of disease

| bone inflammation disease
infectious disease
disease

| bone inflammation disease that has material basis in infection located in bone or located in bone marrow

| [http://www.disease-ontology.org/?id=DOID:1019 DOID:1019]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.160.495 C01.160.495]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.165.495 C05.116.165.495]

| Osteomyelitis

|

|-

| osteonecrosis

| class of disease
symptom or sign

| necrosis
ischemic bone disease
disease

| bone death caused when the bone no longer receives blood supply

| [http://www.disease-ontology.org/?id=DOID:10159 DOID:10159]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.852 C05.116.852]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.550.717.732 C23.550.717.732]

| Aseptic osteonecrosis

| File:Head of femur avascular necrosis.jpg

|-

| osteopoikilosis

| class of disease

| osteosclerosis

| osteosclerosis that results in numerous bone islands located in skeleton

| [http://www.disease-ontology.org/?id=DOID:11991 DOID:11991]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.099.708.702.685 C05.116.099.708.702.685]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.705 C17.300.705]

| Osteopoikilosis

|

|-

| osteoporosis

| class of disease

| bone resorption disease
disease

| bone resorption disease characterized by the thinning of bone tissue and decreased mechanical strength

| [http://www.disease-ontology.org/?id=DOID:11476 DOID:11476]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.198.579 C05.116.198.579]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.452.104.579 C18.452.104.579]

| Osteoporosis

| File:Osteoporosis -- Smart-Servier.jpg

|-

| osteosarcoma

| class of disease

| bone cancer
cell type cancer
bone sarcoma
osteogenic neoplasm
disease
childhood cancer

| bone cancer that is located in bone that has material basis in cells of mesenchymal origin

| [http://www.disease-ontology.org/?id=DOID:3347 DOID:3347]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.565.575.650 C04.557.450.565.575.650]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.450.795.620 C04.557.450.795.620]

| Osteosarcoma

| File:Osteosarcoma.jpg

|-

| osteosarcoma arising in bone Paget's disease

| class of disease

| bone osteosarcoma
mammary Paget's disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7542 DOID:7542]

|

|

|

|-

| osteosclerosis

| class of disease

| bone remodeling disease
disease

| bone remodeling disease that results in abnormal elevated bone density or mass

| [http://www.disease-ontology.org/?id=DOID:4254 DOID:4254]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C05.116.099.708.702 C05.116.099.708.702]

|

| File:ScleroticmetastaticdiseasePelvis.png

|-

| otomycosis

| class of disease
symptom or sign

| otitis externa
dermatomycosis
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0050147 DOID:0050147]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.150.703.658 C01.150.703.658]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.218.736 C09.218.736]

| Otomycosis

| File:Otomycosis.jpg

|-

| otopalatodigital syndrome spectrum disorder

| class of disease

| bone development disease

|

| [http://www.disease-ontology.org/?id=DOID:0111782 DOID:0111782]

|

|

|

|-

| otosclerosis

| class of disease

| inner ear disease
disease

| otitis interna characterized by an abnormal bone growth in the middle ear

| [http://www.disease-ontology.org/?id=DOID:12185 DOID:12185]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.218.768 C09.218.768]

| Otosclerosis

| File:Gray919.png

|-

| otospondylomegaepiphyseal dysplasia, autosomal dominant

| class of disease

| osteochondrodysplasia
autosomal dominant disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080677 DOID:0080677]

|

|

|

|-

| outlet dysfunction constipation

| class of disease

| constipation

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2088 DOID:2088]

|

|

|

|-

| ovarian Brenner tumor

| class of disease

| ovarian benign neoplasm

| ovarian benign neoplasm that has material basis in the surface epithelium of the ovary

| [http://www.disease-ontology.org/?id=DOID:2636 DOID:2636]

|

| Brenner tumour

|

|-

| ovarian Wilms' cancer

| class of disease

| ovarian cancer

| malignant neoplasm of ovary and nephroblastoma that is located in the ovaries

| [http://www.disease-ontology.org/?id=DOID:2153 DOID:2153]

|

|

|

|-

| ovarian angiosarcoma

| class of disease

| angiosarcoma
ovary sarcoma
sarcoma
ovarian cancer

| human disease

| [http://www.disease-ontology.org/?id=DOID:4527 DOID:4527]

|

|

|

|-

| ovarian benign neoplasm

| class of disease

| female reproductive organ benign neoplasm
ovarian neoplasm
endocrine organ benign neoplasm
ovarian disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060112 DOID:0060112]

|

| Benign neoplasms of the ovary

|

|-

| ovarian biphasic or triphasic teratoma

| class of disease

| ovarian germ cell teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6232 DOID:6232]

|

|

|

|-

| ovarian cancer

| class of disease

| female reproductive organ cancer
ovarian neoplasm
ovarian disease
endocrine gland cancer
rare genetic endocrine disease
inherited gynecological tumor
disease

| female reproductive organ cancer that is located in the ovary

| [http://www.disease-ontology.org/?id=DOID:2394 DOID:2394]

|

| Ovarian cancer

| File:Mucinous lmp ovarian tumour intermed mag.jpg

|-

| ovarian carcinoma

| class of disease

| malignant ovarian surface epithelial-stromal neoplasm
carcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:4001 DOID:4001]

|

|

|

|-

| ovarian carcinosarcoma

| class of disease

| malignant ovarian surface epithelial-stromal neoplasm
carcinosarcoma
mixed Müllerian tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6170 DOID:6170]

|

|

|

|-

| ovarian clear cell adenocarcinoma

| class of disease

| ovary adenocarcinoma
clear cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5304 DOID:5304]

|

|

|

|-

| ovarian clear cell adenofibroma

| class of disease

| ovarian benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5897 DOID:5897]

|

|

|

|-

| ovarian clear cell cystadenocarcinoma

| class of disease

| ovarian cystadenocarcinoma
ovarian clear cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7438 DOID:7438]

|

|

|

|-

| ovarian clear cell cystadenofibroma

| class of disease

| ovarian clear cell adenofibroma
clear cell cystadenofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5896 DOID:5896]

|

|

|

|-

| ovarian clear cell malignant adenofibroma

| class of disease

| ovarian cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6554 DOID:6554]

|

|

|

|-

| ovarian cyst

| class of disease

| ovarian disease
ovarian neoplasm
disease

| fluid-filled sac in the ovary

| [http://www.disease-ontology.org/?id=DOID:5119 DOID:5119]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.182.612 C04.182.612]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.056.630.580 C13.351.500.056.630.580]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.630.580 C19.391.630.580]

| Ovarian cysts

| File:Benign Ovarian Cyst.jpg

|-

| ovarian cystadenocarcinoma

| class of disease

| ovary adenocarcinoma
cystadenocarcinoma
ovarian cystadenoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:3605 DOID:3605]

|

|

|

|-

| ovarian cystadenoma

| class of disease

| ovarian benign neoplasm
benign epithelial neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:3269 DOID:3269]

|

|

|

|-

| ovarian cystic teratoma

| class of disease

| mature teratoma of the ovary

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5118 DOID:5118]

|

| Mature cystic teratoma of ovary

|

|-

| ovarian disease

| class of disease

| female reproductive system disease
gonadal disease
adnexal disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1100 DOID:1100]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.056.630 C13.351.500.056.630]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.391.630 C19.391.630]

| Diseases and disorders of ovaries

|

|-

| ovarian dysfunction

| class of disease

| ovarian disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1414 DOID:1414]

|

|

|

|-

| ovarian dysgenesis 1

| class of disease

| autosomal recessive disease
46 XX gonadal dysgenesis

| 46 XX gonadal dysgenesis that has material basis in homozygous or compound heterozygous mutation in the gene encoding follicle-stimulating hormone receptor on chromosome 2p16

| [http://www.disease-ontology.org/?id=DOID:0080493 DOID:0080493]

|

|

|

|-

| ovarian dysgenesis 4

| class of disease

| autosomal recessive disease
46 XX gonadal dysgenesis

| 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the MCM9 gene on chromosome 6q22

| [http://www.disease-ontology.org/?id=DOID:0080496 DOID:0080496]

|

|

|

|-

| ovarian dysgenesis 5

| class of disease

| autosomal recessive disease
46 XX gonadal dysgenesis

| 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the SOHLH1 gene on chromosome 9q34

| [http://www.disease-ontology.org/?id=DOID:0080497 DOID:0080497]

|

|

|

|-

| ovarian dysgenesis 6

| class of disease

| autosomal recessive disease
46 XX gonadal dysgenesis

| 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the NUP107 gene on chromosome 12q15

| [http://www.disease-ontology.org/?id=DOID:0080498 DOID:0080498]

|

|

|

|-

| ovarian dysgenesis 7

| class of disease

| autosomal recessive disease
46 XX gonadal dysgenesis

| 46 XX gonadal dysgenesis that has material basis in homozygous mutation in the MRPS22 gene on chromosome 3q23

| [http://www.disease-ontology.org/?id=DOID:0080499 DOID:0080499]

|

|

|

|-

| ovarian dysgenesis 8

| class of disease

| 46 XX gonadal dysgenesis
autosomal dominant disease

| 46 XX gonadal dysgenesis that has material basis in heterozygous mutation in the ESR2 gene on chromosome 14q23

| [http://www.disease-ontology.org/?id=DOID:0080500 DOID:0080500]

|

|

|

|-

| ovarian embryonal carcinoma

| class of disease

| embryonal carcinoma
malignant non-dysgerminomatous germ cell tumor of ovary
ovarian cancer

| embryonal carcinoma that is located in the ovary

| [http://www.disease-ontology.org/?id=DOID:5681 DOID:5681]

|

|

|

|-

| ovarian endodermal sinus tumor

| class of disease

| ovarian primitive germ cell tumor
malignant non-dysgerminomatous germ cell tumor of ovary
endodermal sinus tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5350 DOID:5350]

|

|

|

|-

| ovarian endometrial cancer

| class of disease

| surface epithelial-stromal tumor
Endometrioid tumor
female reproductive endometrioid cancer

| ovary epithelial cancer that has material basis in the endometrium and is located in the ovary

| [http://www.disease-ontology.org/?id=DOID:6212 DOID:6212]

|

|

|

|-

| ovarian endometrioid adenofibroma

| class of disease

| ovarian benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5480 DOID:5480]

|

|

|

|-

| ovarian endometrioid cystadenofibroma

| class of disease

| ovarian endometrioid adenofibroma
cystadenofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7411 DOID:7411]

|

|

|

|-

| ovarian endometrioid cystadenoma

| class of disease

| ovarian cystadenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7191 DOID:7191]

|

|

|

|-

| ovarian endometrioid malignant adenofibroma

| class of disease

| ovarian carcinosarcoma
malignant adenofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6445 DOID:6445]

|

|

|

|-

| ovarian endometrioid stromal sarcoma

| class of disease

| ovary sarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5169 DOID:5169]

|

|

|

|-

| ovarian fetiform teratoma

| class of disease

| mature teratoma of the ovary

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6314 DOID:6314]

|

|

|

|-

| ovarian germ cell monodermal and highly specialized teratoma

| class of disease

| monodermal teratoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2641 DOID:2641]

|

|

|

|-

| ovarian germ cell neoplasm

| class of disease

| ovarian neoplasm
germ cell tumor
germ cell and embryonal neoplasms
ovarian cancer

| benign or malignant ovarian tumor that originates in the germ (egg) cells of the ovary

| [http://www.disease-ontology.org/?id=DOID:2156 DOID:2156]

|

| Germ cell neoplasms

|

|-

| ovarian germ cell teratoma

| class of disease

| ovarian germ cell neoplasm
teratoma
gonadal teratoma
female reproductive organ cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5567 DOID:5567]

|

| Ovarian teratomas

| File:Teratoma Ovary 4x.jpg

|-

| ovarian gonadoblastoma

| class of disease

| ovarian benign neoplasm
gonadoblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3578 DOID:3578]

|

|

|

|-

| ovarian large-cell neuroendocrine carcinoma

| class of disease

| ovarian carcinoma
familiar ovarian carcinoma
inherited neuroendocrine tumor
large cell neuroendocrine carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4555 DOID:4555]

|

|

|

|-

| ovarian lymphoma

| class of disease

| ovarian cancer
lymphoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2150 DOID:2150]

|

|

|

|-

| ovarian malignant mesothelioma

| class of disease

| ovarian cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2143 DOID:2143]

|

|

|

|-

| ovarian melanoma

| class of disease

| ovarian cancer

| ovarian cancer that has material basis in melanoctyes

| [http://www.disease-ontology.org/?id=DOID:0050928 DOID:0050928]

|

|

|

|-

| ovarian mesodermal adenosarcoma

| class of disease

| ovarian carcinosarcoma
adenosarcoma

| adenosarcoma and malignant ovarian endometroid tumorthat is located in the ovary

| [http://www.disease-ontology.org/?id=DOID:4115 DOID:4115]

|

|

|

|-

| ovarian mixed germ cell neoplasm

| class of disease

| ovarian primitive germ cell tumor
mixed germ cell cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5936 DOID:5936]

|

|

|

|-

| ovarian mucinous adenocarcinoma

| class of disease

| ovary adenocarcinoma
malignant ovarian mucinous tumor
mucinous adenocarcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:3606 DOID:3606]

|

|

|

|-

| ovarian mucinous adenofibroma

| class of disease

| ovarian benign neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:6469 DOID:6469]

|

|

|

|-

| ovarian mucinous cystadenocarcinoma

| class of disease

| ovarian cystadenocarcinoma
mucinous cystadenocarcinoma
ovarian mucinous adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3604 DOID:3604]

|

|

|

|-

| ovarian mucinous cystadenofibroma

| class of disease

| ovarian mucinous adenofibroma
mucinous cystadenofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7013 DOID:7013]

|

|

|

|-

| ovarian mucinous malignant adenofibroma

| class of disease

| malignant ovarian mucinous tumor
malignant adenofibroma
ovarian mucinous neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6278 DOID:6278]

|

|

|

|-

| ovarian mucinous neoplasm

| class of disease

| surface epithelial-stromal tumor
mucinous tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6067 DOID:6067]

|

| Ovarian mucinous tumors

| File:Mucinous lmp ovarian tumour intermed mag.jpg

|-

| ovarian papillary cystadenoma

| class of disease

| ovarian papillary neoplasm
papillary adenoma
ovarian cystadenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6405 DOID:6405]

|

|

|

|-

| ovarian papillary neoplasm

| class of disease

| surface epithelial-stromal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6214 DOID:6214]

|

|

|

|-

| ovarian primitive germ cell tumor

| class of disease

| malignant ovarian germ cell neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5351 DOID:5351]

|

|

|

|-

| ovarian serous adenofibroma

| class of disease

| ovarian benign neoplasm
serous adenofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5474 DOID:5474]

|

|

|

|-

| ovarian serous carcinoma

| class of disease

| ovarian carcinoma
serous carcinoma
ovarian serous tumor

| ovarian carcinoma that has material basis in the lining of the ovary and produces a serum-like fluid

| [http://www.disease-ontology.org/?id=DOID:0050933 DOID:0050933]

|

| Ovarian serous carcinoma

|

|-

| ovarian serous cystadenofibroma

| class of disease

| ovarian serous adenofibroma
cystadenofibroma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7320 DOID:7320]

|

|

|

|-

| ovarian serous cystadenoma

| class of disease

| serous cystadenoma
ovarian benign neoplasm
ovarian cystadenocarcinoma
serous cystadenocarcinoma
ovarian cystadenoma
ovarian serous tumor

| ovary serous adenoma that has material basis in glandular epithelium, in which cystic accumulations of retained secretions are formed

| [http://www.disease-ontology.org/?id=DOID:5746 DOID:5746]
[http://www.disease-ontology.org/?id=DOID:3914 DOID:3914]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.035.320.240 C04.557.470.035.320.240]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.590.485.240 C04.557.470.590.485.240]

| Ovarian serous cystadenoma

| File:Ovarian serous cystadenoma - alt -- low mag.jpg

|-

| ovarian sex cord-stromal tumor

| class of disease

| sex cord-gonadal stromal tumor

| A benign or malignant neoplasm that arises from the ovary and is composed of granulosa cells, Sertoli cells, Leydig cells, theca cells, and fibroblasts. Representative examples include thecoma, fibroma, Sertoli cell tumor, and granulosa cell tumor.

| [http://www.disease-ontology.org/?id=DOID:0080369 DOID:0080369]

|

|

|

|-

| ovarian small cell carcinoma

| class of disease

| ovarian carcinoma
small cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6179 DOID:6179]

|

|

|

|-

| ovarian solid teratoma

| class of disease

| mature teratoma of the ovary

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6315 DOID:6315]

|

|

|

|-

| ovarian squamous cell carcinoma

| class of disease

| ovarian squamous cell neoplasm
squamous cell carcinoma
ovarian cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5531 DOID:5531]

|

|

|

|-

| ovarian squamous cell neoplasm

| class of disease

| surface epithelial-stromal tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5532 DOID:5532]

|

|

|

|-

| ovarian surface papilloma

| class of disease

| ovarian papillary neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6407 DOID:6407]

|

|

|

|-

| ovary adenocarcinoma

| class of disease

| ovarian carcinoma
adenocarcinoma

| ovarian carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:3713 DOID:3713]

|

| Adenocarcinomas of the ovary

| File:Metastatic ovarian adenocarcinoma- Pleural fluid cell block Case 168 (5494503444).jpg

|-

| ovary leiomyosarcoma

| class of disease

| leiomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5263 DOID:5263]

|

|

|

|-

| ovary mixed epithelial carcinoma

| class of disease

| ovarian carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6898 DOID:6898]
[http://www.disease-ontology.org/?id=DOID:6899 DOID:6899]

|

|

|

|-

| ovary neuroendocrine neoplasm

| class of disease

| ovarian cancer
neuroendocrine tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3002 DOID:3002]

|

|

|

|-

| ovary papillary carcinoma

| class of disease

| ovarian papillary neoplasm
ovarian carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6408 DOID:6408]

|

|

|

|-

| ovary rhabdomyosarcoma

| class of disease

| ovary sarcoma
rhabdomyosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4059 DOID:4059]

|

|

|

|-

| ovary sarcoma

| class of disease

| ovarian cancer
sarcoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:2146 DOID:2146]

|

|

|

|-

| ovary serous adenocarcinoma

| class of disease

| ovary adenocarcinoma
ovarian serous carcinoma

| ovary adenocarcinoma that derives from the lining of a cavity that produces a serum-like fluid (a serous cavity)

| [http://www.disease-ontology.org/?id=DOID:5744 DOID:5744]

|

| Serous adenocarcinoma of the ovary

|

|-

| overhydrated hereditary stomatocytosis

| class of disease

| macrocytic anemia
autosomal dominant disease
hereditary stomatocytosis

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111562 DOID:0111562]

|

|

|

|-

| overnutrition

| class of disease

| nutrition disorder
malnutrition

| form of malnutrition in which the intake of nutrients is oversupplied

| [http://www.disease-ontology.org/?id=DOID:654 DOID:654]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.654.726 C18.654.726]

|

|

|-

| ovine and caprine brucellosis

| class of disease

| brucellosis

| A brucellosis that involves an infection caused by Brucella melitensis [NCBITaxon:29459] in cattle, goats, sheep and humans. The disease has symptom fever, has symptom malaise, has symptom anorexia, has symptom limb pain and has symptom back pain.

| [http://www.disease-ontology.org/?id=DOID:14456 DOID:14456]

|

|

|

|-

| oxirane allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger oxirane

| [http://www.disease-ontology.org/?id=DOID:0040082 DOID:0040082]

|

|

|

|-

| oxyphilic adenoma

| class of disease

| endocrine organ benign neoplasm
oncocytic neoplasm
benign epithelial neoplasm
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5389 DOID:5389]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.035.140 C04.557.470.035.140]

| Oncocytoma

| File:Parotid gland oncocytoma - very high mag.jpg

|-

| oxyphilic endometrial endometrioid adenocarcinoma

| class of disease

| endometrial adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6865 DOID:6865]

|

|

|

|-

| pain agnosia

| class of disease

| agnosia
absence of pain sensation

| agnosia that is a loss of the ability to perceive and process pain

| [http://www.disease-ontology.org/?id=DOID:0060145 DOID:0060145]

|

|

|

|-

| pain disorder

| class of disease

| somatoform disorder
disease
pain

| somatoform disorder that involves chronic pain in one or more areas, and is thought to be caused by psychological stress.

| [http://www.disease-ontology.org/?id=DOID:0060164 DOID:0060164]

|

|

|

|-

| palindromic rheumatism

| class of disease

| syndrome
arthritis

| human disease

| [http://www.disease-ontology.org/?id=DOID:1166 DOID:1166]

|

|

|

|-

| palladium allergic contact dermatitis

| class of disease

| allergic contact dermatitis
metal allergy

| allergic contact dermatitis that has allergic trigger palladium

| [http://www.disease-ontology.org/?id=DOID:0040055 DOID:0040055]

|

|

|

|-

| palmoplantar keratosis

| class of disease

| keratosis
foot diseases
epidermal disease
disease

| keratosis characterized by abnormal thickening of the palms and the soles

| [http://www.disease-ontology.org/?id=DOID:3390 DOID:3390]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C16.320.850.475 C16.320.850.475]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.428.435 C17.800.428.435]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.827.475 C17.800.827.475]

| Palmoplantar keratodermas

|

|-

| pancreas disease

| class of disease

| endocrine system disease

| endocrine system disease that is located in the pancreas

| [http://www.disease-ontology.org/?id=DOID:26 DOID:26]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.689 C06.689]

| Diseases and disorders of pancreas

|

|-

| pancreas lymphoma

| class of disease

| pancreatic cancer
lymphoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:1792 DOID:1792]

|

|

|

|-

| pancreas sarcoma

| class of disease

| pancreatic cancer
sarcoma

| pancreatic cancer that is located in the pancreas and that arises from transformed cells of mesenchymal origin

| [http://www.disease-ontology.org/?id=DOID:1796 DOID:1796]

|

|

|

|-

| pancreatic ACTH hormone producing tumor

| class of disease

| islet cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7697 DOID:7697]

|

|

|

|-

| pancreatic acinar cell adenocarcinoma

| class of disease

| pancreatic adenocarcinoma
Acinar cell carcinoma of the pancreas
acinar adenocarcinoma

| pancreatic adenocarcinoma that has material basis in cells with morphological resemblance to acinar cells and is associated with increased serum lipase

| [http://www.disease-ontology.org/?id=DOID:5742 DOID:5742]

|

|

|

|-

| pancreatic adenocarcinoma

| class of disease

| pancreatic carcinoma
adenocarcinoma

| pancreatic carcinoma that derives from epithelial cells of glandular origin

| [http://www.disease-ontology.org/?id=DOID:4074 DOID:4074]

|

| Adenocarcinomas of the pancreas

| File:Metastatic pancreatic adenocarcinoma with lepidic growth pattern Case 280 (9840005374).jpg

|-

| pancreatic cancer

| class of disease

| endocrine gland cancer
pancreas disease
pancreatic neoplasm
gastrointestinal system cancer
disease

| endocrine gland cancer located in the pancreas

| [http://www.disease-ontology.org/?id=DOID:1793 DOID:1793]

|

| Pancreatic cancer

| File:MBq cystic-carcinoma-pancreas.jpg

|-

| pancreatic carcinoma

| class of disease

| pancreatic cancer
carcinoma
gastrointestinal carcinoma

| pancreas cancer that derives from epithelial cells located in the pancreas

| [http://www.disease-ontology.org/?id=DOID:4905 DOID:4905]

|

|

|

|-

| pancreatic cholera

| class of disease

| endocrine pancreas disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6977 DOID:6977]

|

|

|

|-

| pancreatic colloid cystadenocarcinoma

| class of disease

| pancreatic cystadenocarcinoma
mucinous cystadenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7234 DOID:7234]

|

|

|

|-

| pancreatic cystadenocarcinoma

| class of disease

| pancreatic adenocarcinoma
cystadenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4073 DOID:4073]

|

|

|

|-

| pancreatic cystadenoma

| class of disease

| benign neoplasm of exocrine pancreas
endocrine organ benign neoplasm
benign neoplasm of pancreas
gastrointestinal system benign neoplasm
pancreas disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3918 DOID:3918]

|

|

|

|-

| pancreatic delta cell neoplasm

| class of disease

| islet cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4433 DOID:4433]

|

|

|

|-

| pancreatic ductal adenocarcinoma

| class of disease

| pancreatic adenocarcinoma

| pancreatic adenocarcinoma that derives from pancreatic duct cells

| [http://www.disease-ontology.org/?id=DOID:3498 DOID:3498]

|

|

|

|-

| pancreatic ductal carcinoma

| class of disease

| pancreatic cancer
ductal carcinoma
pancreatic carcinoma

| most common cancer of the pancreas

| [http://www.disease-ontology.org/?id=DOID:3587 DOID:3587]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.232.750 C04.557.470.200.025.232.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.615.132.750 C04.557.470.615.132.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.761.750 C04.588.274.761.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.475.750 C04.588.322.475.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.761.750 C06.301.761.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.689.667.625 C06.689.667.625]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.421.750 C19.344.421.750]

|

|

|-

| pancreatic foamy gland adenocarcinoma

| class of disease

| pancreatic adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7577 DOID:7577]

|

|

|

|-

| pancreatic gastrinoma

| class of disease

| islet cell tumor
functional pancreatic neuroendocrine tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5580 DOID:5580]

|

|

|

|-

| pancreatic intraductal papillary-colloid carcinoma

| class of disease

| pancreatic adenocarcinoma
pancreatic intraductal papillary-mucinous neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7574 DOID:7574]

|

|

|

|-

| pancreatic intraductal papillary-mucinous adenoma

| class of disease

| pancreatic intraductal papillary-mucinous neoplasm
adenoma of pancreas
gastrointestinal system benign neoplasm
adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7851 DOID:7851]

|

|

|

|-

| pancreatic intraductal papillary-mucinous neoplasm

| class of disease

| cancer of exocrine pancreas

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7575 DOID:7575]

|

|

|

|-

| pancreatic invasive intraductal papillary-mucinous carcinoma

| class of disease

| pancreatic intraductal papillary-colloid carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8150 DOID:8150]

|

|

|

|-

| pancreatic invasive mucinous cystadenocarcinoma

| class of disease

| pancreatic colloid cystadenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7236 DOID:7236]

|

|

|

|-

| pancreatic mucinous cystadenoma

| class of disease

| mucinous cystadenoma
pancreatic cystadenoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:7235 DOID:7235]

|

|

|

|-

| pancreatic mucinous ductal ectasia

| class of disease

| pancreas disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13313 DOID:13313]

|

|

|

|-

| pancreatic non-functioning delta cell tumor

| class of disease

| pancreatic delta cell neoplasm
non-functioning pancreatic endocrine tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7840 DOID:7840]

|

|

|

|-

| pancreatic non-invasive intraductal papillary-mucinous carcinoma

| class of disease

| pancreatic intraductal papillary-colloid carcinoma
pancreatic intraductal papillary-mucinous neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7685 DOID:7685]

|

|

|

|-

| pancreatic non-invasive mucinous cystadenocarcinoma

| class of disease

| pancreatic colloid cystadenocarcinoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:7237 DOID:7237]

|

|

|

|-

| pancreatic serous cystadenocarcinoma

| class of disease

| pancreatic cystadenocarcinoma
serous cystadenocarcinoma
pancreatic serous cystic neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5751 DOID:5751]

|

|

|

|-

| pancreatic serous cystadenoma

| class of disease

| serous cystadenoma
pancreatic cystadenoma
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3917 DOID:3917]

|

| Serous cystadenoma pancreas

|

|-

| pancreatic serous cystic neoplasm

| class of disease

| pancreatic exocrine neoplasm
Serous tumour
cystic lesions of the pancreas
cancer of exocrine pancreas

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3919 DOID:3919]

|

| Serous cystic neoplasms of the pancreas

|

|-

| pancreatic signet ring cell adenocarcinoma

| class of disease

| pancreatic ductal adenocarcinoma
signet ring cell adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3497 DOID:3497]

|

|

|

|-

| pancreatic solid pseudopapillary carcinoma

| class of disease

| pancreatic carcinoma

| pancreatic carcinoma that is characterized by its papillary architecture

| [http://www.disease-ontology.org/?id=DOID:6827 DOID:6827]

|

|

|

|-

| pancreatic somatostatinoma

| class of disease

| islet cell tumor
pancreatic delta cell neoplasm
somatostatinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4432 DOID:4432]

|

|

|

|-

| pancreatic squamous cell carcinoma

| class of disease

| pancreatic cancer
squamous cell carcinoma

| squamous cell carcinoma located in the pancreas

| [http://www.disease-ontology.org/?id=DOID:0080323 DOID:0080323]

|

|

|

|-

| pancreatic steatorrhea

| class of disease

| pancreas disease
steatorrhea

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10610 DOID:10610]

|

|

|

|-

| pancreatic vasoactive intestinal peptide producing tumor

| class of disease

| islet cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5741 DOID:5741]

|

|

|

|-

| pancreatoblastoma

| class of disease

| pancreatic carcinoma
rare epithelial tumor of pancreas
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6823 DOID:6823]

|

|

|

|-

| pancytopenia

| class of disease

| anemia
cytopenia
disease

| medical condition in which there is a reduction in the number of red and white blood cells, as well as platelets

| [http://www.disease-ontology.org/?id=DOID:12450 DOID:12450]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C15.378.243.875 C15.378.243.875]

|

|

|-

| panhypopituitarism, X-linked

| class of disease

| panhypopituitarism
X-linked disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111779 DOID:0111779]

|

|

|

|-

| panic disorder

| class of disease

| anxiety disorder
disease

| anxiety disorder characterized by reoccurring unexpected panic attacks

| [http://www.disease-ontology.org/?id=DOID:594 DOID:594]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.080.700 F03.080.700]

| Panic disorder

| File:Panic attack.jpg

|-

| panniculitis

| class of disease

| fibromyalgia
connective tissue disease
skin disease
disease

| Inflammation of the subcutaneous adipose tissue

| [http://www.disease-ontology.org/?id=DOID:1526 DOID:1526]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.300.710 C17.300.710]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.566 C17.800.566]

| Panniculitis

| File:An introduction to dermatology (1905) erythema induratum 2.jpg

|-

| panuveitis

| class of disease

| uveitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12030 DOID:12030]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.879.780 C11.941.879.780]

|

|

|-

| papillary adenocarcinoma

| class of disease

| adenocarcinoma

| adenocarcinoma that derives from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue

| [http://www.disease-ontology.org/?id=DOID:3112 DOID:3112]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.085 C04.557.470.200.025.085]

|

|

|-

| papillary adenofibroma

| class of disease

| adenofibroma

| biphasic polypoid neoplasm characterized by the presence of papillary projections that are lined by epithelial cells and fibrotic stroma

| [http://www.disease-ontology.org/?id=DOID:5479 DOID:5479]

|

|

|

|-

| papillary adenoma

| class of disease

| glandular cell epithelial neoplasm
adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3172 DOID:3172]

|

|

|

|-

| papillary carcinoma

| class of disease

| carcinoma

| carcinoma derived from epithelial cells with finger-like projections

| [http://www.disease-ontology.org/?id=DOID:3113 DOID:3113]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.360 C04.557.470.200.360]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.700.360 C04.557.470.700.360]

|

|

|-

| papillary conjunctivitis

| class of disease

| conjunctivitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2458 DOID:2458]

|

|

|

|-

| papillary craniopharyngioma

| class of disease

| craniopharyngioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3847 DOID:3847]

|

|

|

|-

| papillary cystadenocarcinoma

| class of disease

| cystadenocarcinoma
papillary cystic tumor

| cystadenocarcinoma that derives from epithelial cells originating in glandular tissue, with cysts and papillary endophytic projections

| [http://www.disease-ontology.org/?id=DOID:3110 DOID:3110]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.480.230 C04.557.470.200.025.480.230]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.590.480.230 C04.557.470.590.480.230]

|

|

|-

| papillary eccrine adenoma

| class of disease

| eccrine sweat gland neoplasm
papillary adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5446 DOID:5446]

|

|

|

|-

| papillary ependymoma

| class of disease

| benign ependymoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:5505 DOID:5505]

|

|

|

|-

| papillary extrahepatic bile duct adenocarcinoma

| class of disease

| extrahepatic bile duct adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6931 DOID:6931]

|

|

|

|-

| papillary follicular thyroid adenocarcinoma

| class of disease

| papillary thyroid cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3968 DOID:3968]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.060.225 C04.557.470.200.025.060.225]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.085.225 C04.557.470.200.025.085.225]

|

|

|-

| papillary hidradenoma

| class of disease

| hidradenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5439 DOID:5439]

|

| Papillary hidradenoma

| File:Papillary hidradenoma - very high mag.jpg

|-

| papillary meningioma of the cerebellum

| class of disease

| cerebellum cancer
rhabdoid meningioma
papillary meningioma
brain meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5057 DOID:5057]

|

|

|

|-

| papillary pattern testicular yolk sac tumor

| class of disease

| testicular yolk sac tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8193 DOID:8193]

|

|

|

|-

| papillary renal cell carcinomas

| class of disease

| renal cell carcinoma

| renal cell carcinoma that is characterized by the development of multiple, bilateral papillary renal tumors

| [http://www.disease-ontology.org/?id=DOID:4465 DOID:4465]

|

|

| File:Histopathology of papillary renal cell carcinoma type 1, grade 2, with variable density.jpg

|-

| papillary serous adenocarcinoma

| class of disease

| papillary adenocarcinoma

| papillary adenocarcinoma that derives from epithelial cells originating in glandular tissue, which form complex papillary structures with psammoma bodies

| [http://www.disease-ontology.org/?id=DOID:2632 DOID:2632]

|

|

|

|-

| papillary squamous carcinoma

| class of disease

| squamous cell carcinoma
papillary carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4385 DOID:4385]

|

|

|

|-

| papillary thymic adenocarcinoma

| class of disease

| thymus adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5595 DOID:5595]

|

|

|

|-

| papillary thyroid cancer

| class of disease

| thyroid carcinoma
papillary carcinoma
differentiated thyroid carcinoma

| thyroid carcinoma that is characterized by the small mushroom shape of the tumor which has a stem attached to the epithelial layer

| [http://www.disease-ontology.org/?id=DOID:3969 DOID:3969]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.200.025.085.612 C04.557.470.200.025.085.612]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.322.894.400 C04.588.322.894.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.443.915.400 C04.588.443.915.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.344.894.400 C19.344.894.400]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.874.788.400 C19.874.788.400]

| Thyroid papillary carcinoma

|

|-

| papillary transitional carcinoma

| class of disease

| transitional cell carcinoma

| transitional cell carcinoma that has several papillary fronds with central fibrovascular core lined by transitional type epithelium

| [http://www.disease-ontology.org/?id=DOID:4012 DOID:4012]

|

| Urothelial papillary carcinoma

|

|-

| papillary urothelial neoplasm of low malignant potential

| class of disease

| bladder papillary transitional cell neoplasm
urinary tract non-invasive transitional cell neoplasm
papillary urothelial lesion

| human disease

| [http://www.disease-ontology.org/?id=DOID:6239 DOID:6239]

|

|

|

|-

| papilledema

| class of disease

| optic nerve disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:146 DOID:146]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.700.900 C10.292.700.900]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.640.710 C11.640.710]

| Papilledema

| File:Papilledema.jpg

|-

| papilloma

| class of disease

| benign neoplasms by histologic type
papillary tumor
disease

| cell type benign neoplasm that is composed of epithelial tissue on papillae of vascularized connective tissue

| [http://www.disease-ontology.org/?id=DOID:2615 DOID:2615]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.557.470.700.600 C04.557.470.700.600]

| Papillomas

|

|-

| parachordoma

| class of disease

| mesenchymal cell neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2647 DOID:2647]

|

|

|

|-

| paralytic ileus

| class of disease

| bowel obstruction
ileus

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8442 DOID:8442]

|

| Paralytic ileus

|

|-

| paralytic lagophthalmos

| class of disease

| lagophthalmos

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12958 DOID:12958]

|

|

|

|-

| paralytic poliomyelitis

| class of disease

| poliomyelitis
central nervous system disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050515 DOID:0050515]

|

|

|

|-

| paralytic squint

| class of disease

| strabismus
cranial nerve palsy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10863 DOID:10863]

|

|

|

|-

| parameningeal embryonal rhabdomyosarcoma

| class of disease

| embryonal rhabdomyosarcoma

| embryonal rhabdomyosarcoma located in the parameningeal region

| [http://www.disease-ontology.org/?id=DOID:0060338 DOID:0060338]

|

|

|

|-

| parametritis

| class of disease

| pelvic inflammatory diseases
inflammatory disease
uterine disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1260 DOID:1260]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.500.056.750.750 C13.351.500.056.750.750]

|

|

|-

| parametrium malignant neoplasm

| class of disease

| uterine adnexa cancer
broad ligament malignant neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11746 DOID:11746]

|

|

|

|-

| paramyotonia congenita of Von Eulenburg

| class of disease

| neuromuscular disease
autosomal dominant disease
paramyotonia congenita

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111538 DOID:0111538]

|

|

|

|-

| paranasal sinus disease

| class of disease

| nose disease

| respiratory disease

| [http://www.disease-ontology.org/?id=DOID:1352 DOID:1352]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.460.692 C08.460.692]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.603.692 C09.603.692]

|

|

|-

| paranasal sinus lymphoma

| class of disease

| paranasal sinus cancer
lymphoma

| human disease

| [http://www.disease-ontology.org/?id=DOID:1355 DOID:1355]

|

|

|

|-

| paranasal sinus neoplasm

| class of disease

| respiratory tract neoplasm
paranasal sinus disease
respiratory system benign neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:1350 DOID:1350]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.443.665.650.693 C04.588.443.665.650.693]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.460.669.693 C08.460.669.693]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.460.692.503 C08.460.692.503]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C08.785.600.693 C08.785.600.693]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.603.669.693 C09.603.669.693]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.603.692.503 C09.603.692.503]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C09.647.685.693 C09.647.685.693]

| Neoplasms of paranasal sinuses

|

|-

| paranasal sinus sarcoma

| class of disease

| paranasal sinus cancer
sarcoma

| sarcoma and malignant tumor of nasal sinuses that is located in the paranasal sinus

| [http://www.disease-ontology.org/?id=DOID:1362 DOID:1362]

|

|

|

|-

| paraneoplastic pemphigus

| class of disease

| pemphigus

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080852 DOID:0080852]

|

|

|

|-

| paraneoplastic polyneuropathy

| class of disease

| inflammatory and toxic neuropathy
peripheral neuropathy
paraneoplastic neurologic syndrome

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8681 DOID:8681]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.614.550.700 C04.588.614.550.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.730.856.700 C04.730.856.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.574.781.850 C10.574.781.850]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.668.829.800.662 C10.668.829.800.662]

|

|

|-

| paranoid personality disorder

| class of disease

| personality disorder
disease

| mental disorder characterized by paranoia and a pervasive, long-standing suspiciousness and generalized mistrust of others

| [http://www.disease-ontology.org/?id=DOID:10938 DOID:10938]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.675.600 F03.675.600]

| Paranoid personality disorder

|

|-

| parapharyngeal meningioma

| class of disease

| meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8216 DOID:8216]

|

|

|

|-

| paraphilia

| class of disease

| psychosexual disorder
sexual and gender disorder
disease

| experience of intense sexual arousal to atypical objects, situations, or individuals

| [http://www.disease-ontology.org/?id=DOID:0060044 DOID:0060044]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=F03.657 F03.657]

| Paraphilias

| File:Martin van Maele - La Comtesse au fouet 01.jpg

|-

| paraphimosis

| class of disease

| phimosis
disease

| medical condition in which the foreskin of a penis becomes trapped behind the glans penis

| [http://www.disease-ontology.org/?id=DOID:5334 DOID:5334]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.494.684.587 C12.294.494.684.587]

| Paraphimosis

| File:Paraphimosis.jpg

|-

| paraplegia

| class of disease
symptom or sign

| central nervous system disease
paralysis
disease

| impairment in motor or sensory function of the lower extremities

| [http://www.disease-ontology.org/?id=DOID:607 DOID:607]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.597.622.669 C10.597.622.669]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.888.592.636.637 C23.888.592.636.637]

| Paraplegia

|

|-

| parapsoriasis

| class of disease

| psoriasis
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9088 DOID:9088]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.859.575 C17.800.859.575]

|

|

|-

| parasagittal meningioma

| class of disease

| cerebral convexity meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6869 DOID:6869]

|

|

|

|-

| parasitic Ichthyosporea infectious disease

| class of disease

| parasitic infectious diseases

| parasitic infectious disease that involves parasitic infection by the members of the class Ichthyosporea, which are parasites of fish and other animals

| [http://www.disease-ontology.org/?id=DOID:0050291 DOID:0050291]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C03.600 C03.600]

|

|

|-

| parasitic conjunctivitis

| class of disease

| chronic conjunctivitis
parasitic eye infection

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13341 DOID:13341]

|

|

|

|-

| parasitic eyelid infestation

| class of disease

| blepharitis
parasitic eye infection

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13823 DOID:13823]

|

|

|

|-

| parasitic protozoa infectious disease

| class of disease

| parasitic infectious diseases
disease

| parasitic disease caused by a protozoan

| [http://www.disease-ontology.org/?id=DOID:2789 DOID:2789]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.610.752 C01.610.752]

|

|

|-

| paratesticular lipoma

| class of disease

| reproductive organ benign neoplasm
lipoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10207 DOID:10207]

|

|

|

|-

| parathyroid adenoma

| class of disease

| parathyroid neoplasm
benign parathyroid gland neoplasm
benign neoplasms by histologic type
adenoma
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7608 DOID:7608]

|

| Parathyroid adenoma

|

|-

| parathyroid gland disease

| class of disease

| endocrine system disease

| endocrine disease

| [http://www.disease-ontology.org/?id=DOID:11201 DOID:11201]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C19.642 C19.642]

|

|

|-

| parathyroid oncocytic adenoma

| class of disease

| parathyroid adenoma
oxyphilic adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7611 DOID:7611]

|

|

|

|-

| parathyroid transitional clear cell adenoma

| class of disease

| parathyroid adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7609 DOID:7609]

|

|

|

|-

| paraurethral gland cancer

| class of disease

| female reproductive organ cancer
paraurethral gland neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14059 DOID:14059]

|

|

|

|-

| paraurethral gland neoplasm

| class of disease

| urethral benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2139 DOID:2139]

|

|

|

|-

| parenchymatous neurosyphilis

| class of disease

| tertiary neurosyphilis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050490 DOID:0050490]

|

|

|

|-

| parietal lobe ependymoma

| class of disease

| parietal lobe malignant neoplasm
ependymoma

| parietal lobe neoplasm that has material basis in cells lining the ventricles of the brain

| [http://www.disease-ontology.org/?id=DOID:0050903 DOID:0050903]

|

|

|

|-

| paronychia

| class of disease

| nail disease
disease

| bacterial or fungal nail infection of the hand or foot

| [http://www.disease-ontology.org/?id=DOID:13117 DOID:13117]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.539.800.460 C01.539.800.460]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.529.639 C17.800.529.639]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C17.800.838.486 C17.800.838.486]

| Paronychia (disease)

| File:Paronychia.jpg

|-

| parotid disease

| class of disease

| salivary gland disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10302 DOID:10302]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.815.470 C07.465.815.470]

| Diseases and disorders of parotid glands

|

|-

| parotitis

| class of disease

| parotid disease
inflammatory disease
sialadenitis
disease

| parotid disease characterized by the inflammation of one or both parotid glands

| [http://www.disease-ontology.org/?id=DOID:10301 DOID:10301]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.815.470.800 C07.465.815.470.800]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.815.793.500 C07.465.815.793.500]

|

|

|-

| parovarian cyst

| class of disease

| female reproductive system disease
embryonic cyst of fallopian tube

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4333 DOID:4333]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.182.668 C04.182.668]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.300.306.500 C23.300.306.500]

|

|

|-

| paroxysmal nonkinesigenic dyskinesia 2

| class of disease

| Paroxysmal dyskinesia
dystonia
genetic disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0090047 DOID:0090047]

|

|

|

|-

| pars planitis

| class of disease

| intermediate uveitis
chorioretinitis
ciliary body disease
rare genetic eye disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:12731 DOID:12731]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.160.478.700 C11.941.160.478.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.879.780.900.300.659 C11.941.879.780.900.300.659]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.941.879.900.500 C11.941.879.900.500]

|

|

|-

| parthenolide allergic contact dermatitis

| class of disease

| allergic contact dermatitis

| allergic contact dermatitis that has allergic trigger parthenolide

| [http://www.disease-ontology.org/?id=DOID:0040072 DOID:0040072]

|

|

|

|-

| partial androgen insensitivity syndrome

| class of disease

| X-linked recessive disease
androgen insensitivity syndrome

| medical condition

| [http://www.disease-ontology.org/?id=DOID:0080776 DOID:0080776]

|

|

|

|-

| partial arterial retinal occlusion

| class of disease

| retinal artery occlusion

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14522 DOID:14522]

|

|

|

|-

| partial circumpapillary choroid dystrophy

| class of disease

| hereditary choroidal atrophy

| human disease

| [http://www.disease-ontology.org/?id=DOID:9811 DOID:9811]

|

|

|

|-

| partial lipodystrophy

| class of disease

| lipodystrophy

| lipodystrophy that is characterized by partial loss of adipose tissue

| [http://www.disease-ontology.org/?id=DOID:0080299 DOID:0080299]

|

|

|

|-

| partial motor epilepsy

| class of disease

| focal epilepsy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3327 DOID:3327]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490.360.272 C10.228.140.490.360.272]

|

|

|-

| partial optic atrophy

| class of disease

| optic atrophy

| human disease

| [http://www.disease-ontology.org/?id=DOID:10631 DOID:10631]

|

|

|

|-

| partial pancreatic agenesis

| class of disease

| pancreas disease
agenesis
pancreatic agenesis

| pancreas disease that is characterized by the failure of the pancreas to develop prior to birth

| [http://www.disease-ontology.org/?id=DOID:0050877 DOID:0050877]

|

|

|

|-

| partial retinal vein occlusion

| class of disease

| retinal vein occlusion

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1726 DOID:1726]

|

|

|

|-

| partial sensory epilepsy

| class of disease

| focal epilepsy

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3330 DOID:3330]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.228.140.490.360.275 C10.228.140.490.360.275]

|

|

|-

| partial third-nerve palsy

| class of disease

| paralytic squint
oculomotor nerve paralysis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10864 DOID:10864]

|

|

|

|-

| patellar tendinitis

| class of disease

| tendinitis
knee disorder
knee extensor tendonitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10471 DOID:10471]

|

| Patellar tendinitis

|

|-

| patent blue V allergy

| class of disease

| drug allergy

| drug allergy that has allergic trigger patent blue V

| [http://www.disease-ontology.org/?id=DOID:0040080 DOID:0040080]

|

|

|

|-

| paternal uniparental disomy of chromosome 14

| class of disease

| uniparental disomy of paternal origin
uniparental disomy 14
syndrome

| human disease

| [http://www.disease-ontology.org/?id=DOID:0111712 DOID:0111712]

|

|

|

|-

| pathologic nystagmus

| class of disease

| nystagmus
ocular motility disease
abnormal eye movements

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9650 DOID:9650]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.292.562.675 C10.292.562.675]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C11.590.400 C11.590.400]

|

|

|-

| patterned macular dystrophy 1

| class of disease

| patterned macular dystrophy

| human disease

| [http://www.disease-ontology.org/?id=DOID:0060866 DOID:0060866]

|

|

|

|-

| patulous eustachian tube

| class of disease
physiological condition

| eustachian tube disease

| eustachian tube disorder

| [http://www.disease-ontology.org/?id=DOID:12358 DOID:12358]

|

|

|

|-

| peach allergy

| class of disease

| fruit allergy

| fruit allergy triggered by Prunus persica plant fruit food product.

| [http://www.disease-ontology.org/?id=DOID:0060510 DOID:0060510]

|

|

|

|-

| peanut allergy

| class of disease

| tree nut allergy
legume allergy
vegetable allergy

| type of food allergy caused by peanuts

| [http://www.disease-ontology.org/?id=DOID:4378 DOID:4378]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C20.543.480.370.572.750 C20.543.480.370.572.750]

|

| File:Nut warning 1.jpg

|-

| pediatric CNS choriocarcinoma

| class of disease

| malignant childhood germ cell neoplasm
central nervous system choriocarcinoma
rare childhood malignant neoplasm
choriocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6639 DOID:6639]

|

|

|

|-

| pediatric CNS embryonal cell carcinoma

| class of disease

| central nervous system childhood germ cell tumor
central nervous system embryonal carcinoma
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm
brain cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7231 DOID:7231]

|

|

|

|-

| pediatric angiosarcoma

| class of disease

| angiosarcoma
rare childhood malignant neoplasm

| angiosarcoma that affects children

| [http://www.disease-ontology.org/?id=DOID:4505 DOID:4505]

|

|

|

|-

| pediatric cerebral ependymoblastoma

| class of disease

| ependymoblastoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7841 DOID:7841]

|

|

|

|-

| pediatric ependymoma

| class of disease

| ependymoma
childhood cancer
ependymal tumor
childhood neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:5509 DOID:5509]

|

|

|

|-

| pediatric epithelioid sarcoma

| class of disease

| epithelioid sarcoma
rare childhood malignant neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7095 DOID:7095]

|

|

|

|-

| pediatric fibrosarcoma

| class of disease

| fibrosarcoma
rare childhood malignant neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3520 DOID:3520]

|

|

|

|-

| pediatric germ cell tumor

| class of disease

| germ cell tumor
childhood neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6053 DOID:6053]

|

|

|

|-

| pediatric hepatocellular carcinoma

| class of disease

| hepatocellular carcinoma
childhood cancer of liver

| Pediatric hepatocellular carcinoma (pediatric HCC) is a rare, aggressive, malignant hepatic tumor that develops mainly in children over 10 years of age

| [http://www.disease-ontology.org/?id=DOID:0070322 DOID:0070322]

|

|

|

|-

| pediatric infratentorial ependymoblastoma

| class of disease

| childhood infratentorial neoplasm
ependymoblastoma
infratentorial cancer
childhood central nervous system primitive neuroectodermal neoplasm
rare childhood malignant neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7522 DOID:7522]

|

|

|

|-

| pediatric infratentorial ependymoma

| class of disease

| infratentorial cancer
pediatric ependymoma
brain ependymoma
childhood infratentorial neoplasm
childhood cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7501 DOID:7501]

|

|

|

|-

| pediatric leptomeningeal melanoma

| class of disease

| meningeal melanoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6089 DOID:6089]

|

|

|

|-

| pediatric liposarcoma

| class of disease

| liposarcoma
rare childhood malignant neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5695 DOID:5695]

|

|

|

|-

| pediatric low-grade glioma

| class of disease

| low grade glioma

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080830 DOID:0080830]

|

|

|

|-

| pediatric lymphoma

| class of disease

| lymphoma
rare childhood malignant neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5823 DOID:5823]

|

|

|

|-

| pediatric meningioma

| class of disease

| meningioma
pediatric central nervous system tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4593 DOID:4593]

|

|

|

|-

| pediatric mesenchymal chondrosarcoma

| class of disease

| mesenchymal chondrosarcoma
childhood cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4546 DOID:4546]

|

|

|

|-

| pediatric myxoid chondrosarcoma

| class of disease

| myxoid chondrosarcoma
childhood cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6494 DOID:6494]

|

|

|

|-

| pediatric osteosarcoma

| class of disease

| osteosarcoma
rare childhood malignant neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3361 DOID:3361]

|

|

|

|-

| pediatric ovarian dysgerminoma

| class of disease

| pediatric ovarian germ cell tumor
rare childhood malignant neoplasm
malignant childhood germ cell neoplasm
dysgerminoma of ovary

| dysgerminoma of ovary that occurs in children

| [http://www.disease-ontology.org/?id=DOID:7340 DOID:7340]

|

|

|

|-

| pediatric ovarian germ cell tumor

| class of disease

| ovarian germ cell neoplasm
pediatric germ cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6084 DOID:6084]

|

|

|

|-

| pediatric supratentorial ependymoma

| class of disease

| supratentorial cancer
pediatric ependymoma
brain ependymoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7502 DOID:7502]

|

|

|

|-

| pediatric testicular germ cell tumor

| class of disease

| testicular germ cell tumor
pediatric germ cell tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6082 DOID:6082]

|

|

|

|-

| peliosis hepatis

| class of disease

| hepatic vascular disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:914 DOID:914]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.552.802 C06.552.802]

| Peliosis hepatis

|

|-

| pellagra

| class of disease

| nutritional deficiency disease
other acquired skin disease
skin disease
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8457 DOID:8457]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C18.654.521.500.133.699.529 C18.654.521.500.133.699.529]

| Pellagra

| File:Pellagra NIH.jpg

|-

| pelvic inflammatory diseases

| class of disease

| female reproductive system disease
adnexal disease
infectious disease
disease

| infection of uterus, fallopian tubes, ovaries or the inner surface of pelvis

| [http://www.disease-ontology.org/?id=DOID:1003 DOID:1003]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.635.500 C01.635.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.050.351.500.056.750 C12.050.351.500.056.750]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.100.250.056.750 C12.100.250.056.750]

| Pelvic inflammatory disease

| File:Blausen 0732 PID-Sites.png

|-

| pelvic lipomatosis

| class of disease

| lipomatosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3927 DOID:3927]

|

|

|

|-

| pelvic muscle wasting

| class of disease

| pelvic organ prolapse
pelvic floor dysfunction

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11629 DOID:11629]

|

|

|

|-

| pelvic organ prolapse

| class of disease

| female reproductive system disease
prolapse

| pelvic organs protruding from the opening of the vagina

| [http://www.disease-ontology.org/?id=DOID:1284 DOID:1284]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C23.300.842.624 C23.300.842.624]

| Female genital prolapse

| File:Hippocrates treatment for prolapse.png

|-

| pelvic varices

| class of disease

| varicose veins

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9742 DOID:9742]

|

|

|

|-

| pemphigoid

| class of disease

| autoimmune skin disease
bullous skin disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:0080841 DOID:0080841]

|

|

|

|-

| penicillin drug reaction

| class of disease

| adverse drug reaction
beta-lactam allergy
Side effects of penicillin

| beta-lactam allergy triggered by penicillin

| [http://www.disease-ontology.org/?id=DOID:0060520 DOID:0060520]

|

|

|

|-

| penicilliosis

| class of disease

| opportunistic mycosis
disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050288 DOID:0050288]

|

|

|

|-

| penile cancer

| class of disease

| penile neoplasm
male reproductive organ cancer
penile disease
disease

| cancer of the penis

| [http://www.disease-ontology.org/?id=DOID:11615 DOID:11615]

|

| Penile cancer

| File:Penile cancer 2.jpg

|-

| penile disease

| class of disease

| male reproductive system disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:1529 DOID:1529]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.494 C12.294.494]

|

|

|-

| penile neoplasm

| class of disease

| male reproductive system neoplasm
penile disease
male reproductive organ benign neoplasm

| human disease

| [http://www.disease-ontology.org/?id=DOID:11624 DOID:11624]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.945.440.715 C04.588.945.440.715]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.260.500 C12.294.260.500]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.294.494.591 C12.294.494.591]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.758.409.500 C12.758.409.500]

| Penile neoplasms

|

|-

| penile urethral cancer

| class of disease

| male urethral cancer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8223 DOID:8223]

|

|

|

|-

| penis Paget's disease

| class of disease

| penis carcinoma
extramammary Paget's disease
adenocarcinoma of penis
genetic urogenital tumor

| Human disease

| [http://www.disease-ontology.org/?id=DOID:3448 DOID:3448]

|

| Penile Paget's disease

|

|-

| penis basal cell carcinoma

| class of disease

| penis carcinoma
basal-cell carcinoma
rare skin disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:4277 DOID:4277]

|

|

|

|-

| penis basaloid carcinoma

| class of disease

| penis squamous cell carcinoma
basaloid squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7047 DOID:7047]

|

|

|

|-

| penis carcinoma

| class of disease

| penile cancer
carcinoma

| penile cancer that is located in the skin or tissues of the penis

| [http://www.disease-ontology.org/?id=DOID:3449 DOID:3449]

|

|

|

|-

| penis carcinoma in situ

| class of disease

| in situ carcinoma
penile disease
penis squamous cell carcinoma
carcinoma in situ of male genital organs

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8872 DOID:8872]

|

|

|

|-

| penis mixed squamous cell carcinoma

| class of disease

| penis squamous cell carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8009 DOID:8009]

|

|

|

|-

| penis non-invasive verrucous carcinoma

| class of disease

| penis verrucous carcinoma
penis carcinoma in situ
cervical verrucous carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5907 DOID:5907]

|

|

|

|-

| penis papillary carcinoma

| class of disease

| penis squamous cell carcinoma
papillary squamous carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8013 DOID:8013]

|

|

|

|-

| penis sarcoma

| class of disease

| penile cancer
sarcoma

| sarcoma and malignant neoplasm of penis that is located in the penis

| [http://www.disease-ontology.org/?id=DOID:11838 DOID:11838]

|

|

|

|-

| penis squamous cell carcinoma

| class of disease

| penis carcinoma
squamous cell carcinoma

| penis carcinoma that has material basis in squamous cells

| [http://www.disease-ontology.org/?id=DOID:5518 DOID:5518]

|

| Squamous-cell carcinoma of the penis

|

|-

| penis verrucous carcinoma

| class of disease

| penis squamous cell carcinoma
verrucous carcinoma
penis papillary carcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5908 DOID:5908]

|

|

|

|-

| peptic esophagitis

| class of disease

| peptic ulcer disease
esophagitis
gastroesophageal reflux disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:13976 DOID:13976]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.117.620.420 C06.405.117.620.420]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.205.663.420 C06.405.205.663.420]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.275.800.523 C06.405.469.275.800.523]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.586.524 C06.405.748.586.524]

|

|

|-

| peptic ulcer disease

| class of disease

| gastrointestinal system disease
duodenal disease
disease

| ulcer of an area of the gastrointestinal tract

| [http://www.disease-ontology.org/?id=DOID:750 DOID:750]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.275.800 C06.405.469.275.800]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.586 C06.405.748.586]

| Peptic ulcers

| File:Benign gastric ulcer 1.jpg

|-

| perforated corneal ulcer

| class of disease

| corneal ulcer

| Human disease

| [http://www.disease-ontology.org/?id=DOID:10445 DOID:10445]

|

|

|

|-

| perforated ulcer

| class of disease

| peptic ulcer disease
gastric perforation

| medical condition of the gastrointestinal tract wall

| [http://www.disease-ontology.org/?id=DOID:752 DOID:752]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.275.800.698 C06.405.469.275.800.698]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.748.586.698 C06.405.748.586.698]

|

| File:DU 2.jpg

|-

| perforation of bile duct

| class of disease

| biliary tract disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:13409 DOID:13409]

|

|

|

|-

| periampullary adenocarcinoma

| class of disease

| ampulla of Vater adenocarcinoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8110 DOID:8110]

|

|

|

|-

| periampullary adenoma

| class of disease

| ampulla of Vater neoplasm
adenoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:0050849 DOID:0050849]

|

|

|

|-

| perianal gland tumor

| class of disease

| cancer in dogs
anus neoplasm

| dog disease

| [http://www.disease-ontology.org/?id=DOID:4550 DOID:4550]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.083 C04.588.083]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C04.588.274.476.411.307.790.040.040 C04.588.274.476.411.307.790.040.040]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.301.371.411.307.790.040.040 C06.301.371.411.307.790.040.040]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.249.411.307.790.040.040 C06.405.249.411.307.790.040.040]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.491.307.790.040.040 C06.405.469.491.307.790.040.040]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.860.101.163.083 C06.405.469.860.101.163.083]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C06.405.469.860.180.500.040.040 C06.405.469.860.180.500.040.040]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C22.073 C22.073]

|

|

|-

| perianal hematoma

| class of disease

| hemorrhoid

| Human disease

| [http://www.disease-ontology.org/?id=DOID:9745 DOID:9745]

|

| Perianal hematoma

|

|-

| perianal skin Paget's disease

| class of disease

| anal margin carcinoma
extramammary Paget's disease
anal Paget's disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7708 DOID:7708]

|

|

|

|-

| periapical abscess

| class of disease

| periapical periodontitis
dental abscess

| localized collection of pus associated with a tooth

| [http://www.disease-ontology.org/?id=DOID:2562 DOID:2562]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C01.539.830.025.650 C01.539.830.025.650]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.320.830.700.700 C07.320.830.700.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.306.700.700 C07.465.714.306.700.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.533.487.700 C07.465.714.533.487.700]

|

|

|-

| periapical periodontitis

| class of disease

| inflammation
periodontitis
dental pulp disease
periapical disease
tooth pathology

| Human disease

| [http://www.disease-ontology.org/?id=DOID:823 DOID:823]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.320.830.700 C07.320.830.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.306.700 C07.465.714.306.700]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.533.487 C07.465.714.533.487]

|

|

|-

| pericardial effusion

| class of disease
symptom or sign

| pericardium disease
cardiovascular system symptom
disease

| pericardium disease that is characterized by an abnormal accumulation of fluid in the pericardial cavity

| [http://www.disease-ontology.org/?id=DOID:118 DOID:118]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.695 C14.280.695]

| Pericardial effusion

|

|-

| pericardial mesothelioma

| class of disease

| pericardium cancer
mesothelioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6201 DOID:6201]

|

|

|

|-

| pericarditis

| class of disease

| pericardium disease
inflammation
inflammatory disease
heart disease
disease

| pericardium disease that is characterized by an inflammation of the pericardium and has symptom chest pain

| [http://www.disease-ontology.org/?id=DOID:1787 DOID:1787]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C14.280.720 C14.280.720]

| Pericarditis

| File:Pericarditis10.JPG

|-

| pericardium cancer

| class of disease

| heart cancer
neoplasm of pericardium
pericardium disease

| Human disease

| [http://www.disease-ontology.org/?id=DOID:116 DOID:116]

|

|

|

|-

| pericardium leiomyoma

| class of disease

| leiomyoma
benign neoplasm of pericardium
pericardium disease
cardiovascular organ benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5137 DOID:5137]

|

|

|

|-

| pericholangitis

| class of disease

| ascending cholangitis
primary sclerosing cholangitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:14272 DOID:14272]

|

|

|

|-

| perichondritis of auricle

| class of disease

| otitis externa
acquired deformities of the ear

| Human disease

| [http://www.disease-ontology.org/?id=DOID:222 DOID:222]

|

| Perichondritis

|

|-

| pericoronitis

| class of disease

| gingival disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3671 DOID:3671]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.258.771 C07.465.714.258.771]

| Pericoronitis

|

|-

| periductal breast myoepitheliosis

| class of disease

| breast myoepitheliosis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:7520 DOID:7520]

|

|

|

|-

| perinatal intestinal perforation

| class of disease

| intestinal perforation
perinatal digestive system disorder

| Human disease

| [http://www.disease-ontology.org/?id=DOID:2073 DOID:2073]

|

|

|

|-

| perinatal jaundice due to hepatocellular damage

| class of disease

| neonatal jaundice
Neonatal hepatitis

| Human disease

| [http://www.disease-ontology.org/?id=DOID:11452 DOID:11452]

|

|

|

|-

| perineocele

| class of disease

| pelvic organ prolapse

| human disease

| [http://www.disease-ontology.org/?id=DOID:12637 DOID:12637]

|

|

|

|-

| perinephritis

| class of disease

| kidney disease
inflammatory disease
connective tissue disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:2982 DOID:2982]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C12.777.419.685 C12.777.419.685]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C13.351.968.419.685 C13.351.968.419.685]

|

|

|-

| perineural angioma

| class of disease

| deep angioma
hemangioma
central nervous system organ benign neoplasm

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8331 DOID:8331]

|

|

|

|-

| perineurioma

| class of disease

| nerve sheath neoplasms

| Human disease

| [http://www.disease-ontology.org/?id=DOID:4697 DOID:4697]

|

| Perineuroma

|

|-

| periocular meningioma

| class of disease

| meningioma
intraorbital meningioma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:8030 DOID:8030]

|

|

|

|-

| periodic limb movement disorder

| class of disease
symptom or sign

| sleep disorder
disease

| sleep disorder that involves involuntary limb movement during sleep

| [http://www.disease-ontology.org/?id=DOID:9207 DOID:9207]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.886.425.800.600 C10.886.425.800.600]
[http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C10.886.659.618 C10.886.659.618]

|

|

|-

| periodontal disease

| class of disease

| tooth pathology
jaw disease
disease

| human disease

| [http://www.disease-ontology.org/?id=DOID:3388 DOID:3388]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714 C07.465.714]

|

| File:Gingivitis (crop).jpg

|-

| periodontitis

| class of disease

| periodontal disease
disease

| gum disease

| [http://www.disease-ontology.org/?id=DOID:824 DOID:824]

| [http://l.academicdirect.org/Medicine/Informatics/MESH/browse/tree/?t=C07.465.714.533 C07.465.714.533]

| Periodontitis

| File:Paro1.JPG

|-

| periodontosis

| class of disease

| periodontal disease
tooth pathology

| human disease

| [http://www.disease-ontology.org/?id=DOID:9893 DOID:9893]

|

|

|

|-

| periosteal chondrosarcoma

| class of disease

| chondrosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:5859 DOID:5859]

|

|

|

|-

| periosteal osteogenic sarcoma

| class of disease

| peripheral osteosarcoma

| Human disease

| [http://www.disease-ontology.org/?id=DOID:6489 DOID:6489]

|

|

|

|-

| periostitis

| ''[[:d:Q112193867|class of disea