:Template:Congenital malformations and deformations of integument
{{Navbox
| name = Congenital malformations and deformations of integument
| title = Congenital malformations and deformations of integument / skin disease
| state = {{{state
| listclass = hlist
| group1 = Genodermatosis
| list1 = {{Navbox|subgroup
| group1 = Congenital ichthyosis/
erythrokeratodermia
| list1 = {{Navbox|subgroup
| group1 = AD
| list1 =
| group2 = AR
| list2 =
- Congenital ichthyosiform erythroderma: Epidermolytic hyperkeratosis
- Lamellar ichthyosis
- Harlequin-type ichthyosis
| group3 = XR
| list3 =
| group4 = Ungrouped
| list4 =
- Ichthyosis bullosa of Siemens
- Ichthyosis follicularis
- Ichthyosis prematurity syndrome
- Ichthyosis–sclerosing cholangitis syndrome
- Nonbullous congenital ichthyosiform erythroderma
- Ichthyosis linearis circumflexa
- Ichthyosis hystrix
}}
| group3 = EB
and related
| list3 =
| group4 = Ectodermal dysplasia
| list4 =
- Naegeli syndrome/Dermatopathia pigmentosa reticularis
- Hay–Wells syndrome
- Hypohidrotic ectodermal dysplasia
- Focal dermal hypoplasia
- Ellis–van Creveld syndrome
- Rapp–Hodgkin syndrome/Hay–Wells syndrome
| group5 = Elastic/Connective
| list5 =
- Ehlers–Danlos syndrome
- Cutis laxa (Gerodermia osteodysplastica)
- Popliteal pterygium syndrome
- Pseudoxanthoma elasticum
- Van der Woude syndrome
| group6 = Hyperkeratosis/
keratinopathy
| list6 = {{Navbox|subgroup
| evenodd = swap
| group1 = PPK
| list1 =
- diffuse: Diffuse epidermolytic palmoplantar keratoderma
- Diffuse nonepidermolytic palmoplantar keratoderma
- Palmoplantar keratoderma of Sybert
- Meleda disease
- syndromic
- connexin
- Bart–Pumphrey syndrome
- Clouston's hidrotic ectodermal dysplasia
- Vohwinkel syndrome
- Corneodermatoosseous syndrome
- plakoglobin
- Naxos syndrome
- Scleroatrophic syndrome of Huriez
- Olmsted syndrome
- Cathepsin C
- Papillon–Lefèvre syndrome
- Haim–Munk syndrome
- Camisa disease
- focal: Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
- Focal palmoplantar and gingival keratosis
- Howel–Evans syndrome
- Pachyonychia congenita
- Pachyonychia congenita type I
- Pachyonychia congenita type II
- Striate palmoplantar keratoderma
- Tyrosinemia type II
- punctate: Acrokeratoelastoidosis of Costa
- Focal acral hyperkeratosis
- Keratosis punctata palmaris et plantaris
- Keratosis punctata of the palmar creases
- Schöpf–Schulz–Passarge syndrome
- Porokeratosis plantaris discreta
- Spiny keratoderma
- ungrouped: Palmoplantar keratoderma and spastic paraplegia
- desmoplakin
- Carvajal syndrome
- connexin
- Erythrokeratodermia variabilis
- HID/KID
| group2 = Other
| list2 =
- Dyskeratosis congenita
- Keratolytic winter erythema
- Keratosis follicularis spinulosa decalvans
- Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome
- Keratosis pilaris atrophicans faciei
- Keratosis pilaris
}}
| group8 = Other
| list8 =
- cadherin
- EEM syndrome
- immune system
- Hereditary lymphedema
- Mastocytosis/Urticaria pigmentosa
- Hailey–Hailey
see also Template:Congenital malformations and deformations of skin appendages, Template:Phakomatoses, Template:Pigmentation disorders, Template:DNA replication and repair-deficiency disorder
}}
| group2 = Developmental
anomalies
| list2 = {{Navbox|subgroup
| group1 = Midline
| list1 =
| group2 = Nevus
| list2 =
| group3 = Other/ungrouped
| list3 =
- Accessory nail of the fifth toe
- Bronchogenic cyst
- Congenital cartilaginous rest of the neck
- Congenital hypertrophy of the lateral fold of the hallux
- Congenital lip pit
- Congenital malformations of the dermatoglyphs
- Congenital preauricular fistula
- Congenital smooth muscle hamartoma
- Cystic lymphatic malformation
- Median raphe cyst
- Melanotic neuroectodermal tumor of infancy
- Mongolian spot
- Nasolacrimal duct cyst
- Omphalomesenteric duct cyst
- Poland anomaly
- Rapidly involuting congenital hemangioma
- Rosenthal–Kloepfer syndrome
- Skin dimple
- Superficial lymphatic malformation
- Thyroglossal duct cyst
- Verrucous vascular malformation
- Birthmark
}}
}}
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