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