:Template:Disorders of translation and posttranslational modification

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| name = Disorders of translation and posttranslational modification

| title = Disorders of translation and posttranslational modification

| state = {{{state|autocollapse}}}

| bodyclass = hlist

| group1 = Translation

| list1 =

• Ribosome: Diamond–Blackfan anemia
• FMR1
• Fragile X syndrome
• Fragile X-associated tremor/ataxia syndrome
• Premature ovarian failure 1

• Initiation factor: Leukoencephalopathy with vanishing white matter

• snRNP: Retinitis pigmentosa 33

| group2 = Posttranslational modification

| list2 =

{{Navbox|subgroup

| group1 = Protein folding

| list1 =

• Alzheimer's disease
• Huntington's disease
• Creutzfeldt–Jakob disease

• chaperonins: 3-Methylglutaconic aciduria 5

| group2 = Protein targeting

| list2 =

• I-cell disease

| group3 = Ubiquitin

| list3 =

• E1: X-linked spinal muscular atrophy 2

• E3: Johanson–Blizzard syndrome
• Von Hippel–Lindau disease
• 3-M syndrome
• Angelman syndrome

• Deubiquitinating enzyme: Machado–Joseph disease
• Aneurysmal bone cyst
• Multiple familial trichoepithelioma 1

| group4 = SUMO

| list4 =

• OFC10

| group5 = Other

| list5 =

• Multiple sulfatase deficiency
• Hyperproinsulinemia
• Ehlers–Danlos syndrome 6

}}

}}

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Category:Disorders of synthesis of DNA, RNA, and proteins

Category:Genetic disease and disorder templates by mechanism