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Spinocerebellar ataxia type 32

Disease definition

Spinocerebellar ataxia type 32 (SCA32) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1; see this term) characterized by ataxia, cognitive impairment and azoospermia in males.

ORPHA:276183

Classification level: Disorder
  • Synonym(s):
    • Cerebellar ataxia with azoospermia and intellectual disability
    • SCA32
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Adult
  • ICD-10: G11.8
  • OMIM: 613909
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -

Detailed information

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