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Spinocerebellar ataxia type 4

Disease definition

Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term) characterized by ataxia with sensory neuropathy.

ORPHA:98765

Classification level : Disorder
  • Synonym(s):
    • SCA4
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant 
  • Age of onset: Adult
  • ICD-10: G11.2
  • OMIM: 600223
  • UMLS: C0752122
  • MeSH: -
  • GARD: 9970
  • MedDRA: -

Detailed information

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