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Spinocerebellar ataxia type 35

Disease definition

Spinocerebellar ataxia type 35 (SCA35) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1; see this term) characterized by the adult-onset of progressive gait and limb ataxia, dysarthria, ocular dysmetria, intention tremor, hyperreflexia and spasmodic torticollis.

ORPHA:276193

  • Synonym(s):
    • SCA35
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Adult
  • ICD-10: G11.8
  • OMIM: 613908
  • UMLS: -
  • MeSH: -
  • GARD: 12366
  • MedDRA: -

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