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Autosomal dominant cerebellar ataxia type I

Disease definition

A group of spinocerebellar ataxias (SCAs) characterized by ataxia with other neurological signs, including oculomotor disturbances, cognitive deficits, pyramidal and extrapyramidal dysfunction, bulbar, spinal and peripheral nervous system involvement.

ORPHA:94145

Classification level: Group of disorders
  • Synonym(s):
    • ADCA1
    • ADCAI
    • Autosomal dominant cerebellar ataxia type 1
    • Cerebellar plus syndrome
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant 
  • Age of onset: All ages
  • ICD-10: G11.8
  • OMIM: -
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -

Detailed information

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