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Template:Disorders of translation and posttranslational modification

From WikiMD's medical encyclopedia

Disorders of translation and posttranslational modification
Translation
* 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
Posttranslational modification
Protein folding
* Alzheimer's disease
  • Huntington's disease
  • Creutzfeldt–Jakob disease
  • chaperonins: 3-Methylglutaconic aciduria 5
Protein targeting
* I-cell disease
Ubiquitin
* 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
SUMO
* OFC10
Other
* Multiple sulfatase deficiency
  • Hyperproinsulinemia
  • Ehlers–Danlos syndrome 6


Retrieved from "https://wikimd.org/w/index.php?title=Template:Disorders_of_translation_and_posttranslational_modification&oldid=6445066"
Categories:
  • Disorders of synthesis of DNA, RNA, and proteins
  • Genetic disease and disorder templates by mechanism
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  • This page was last edited on 8 March 2025, at 18:47.
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