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Dentatorubral pallidoluysian atrophy

^ http://www.orpha.net/ORDO/Orphanet_101


Dentatorubral pallidoluysian atrophy (DRPLA) is a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by involuntary movements, ataxia, epilepsy, mental disorders, cognitive decline and prominent anticipation.

Synonyms: DRPLA, Naito-Oyanagi disease, Dentatorubropallidoluysian atrophy

Term info

database cross reference
  • ICD-10:G11.8 (NTBT (narrower term maps to a broader term))
  • UMLS:C0751781 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:G11.8 (Attributed)
  • OMIM:125370 (E (exact mapping (the terms and the concepts are equivalent)))
hasDbXref

ICD-10:G11.8, OMIM:125370, UMLS:C0751781

notation

ORPHA:101