A very rare, autosomal dominant inherited neurodegenerative disorder. Signs and symptoms include ataxia, spasticity, and abnormalities in the ocular movements. [ NCI ]

Synonyms:

SCA3

Machado-Joseph Disease

Spinocerebellar Ataxia Type 3

This is just here as a test because I lose it

Term information

Subsets

NCIT_C165258

Contributing Source
  • Cellosaurus
Preferred Name
  • Spinocerebellar Ataxia Type 3
Semantic Type
  • Disease or Syndrome
UMLS CUI
  • C0024408
code
  • C84830