autosomal dominant cerebellar ataxia type III
MONDO:0019793Mondo
Findings
No curated finding names autosomal dominant cerebellar ataxia type III yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Autosomal dominant cerebellar ataxia (ACDA) type III is a group of neurodegenerative disorders characterized by mostly pure cerebellar syndromes with occasional non-cerebellar signs (e.g. pyramidal signs, peripheral neuropathy, writer's cramp) and includes spinocerebellar ataxia (SCA) type 5 (SCA5), SCA6, SCA11, SCA26, SCA30, and SCA31.
Definition from the Mondo Disease Ontology (MONDO:0019793), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
- Narrower terms (10)
Other names
4 names
Resolves to: autosomal dominant cerebellar ataxia type III
- Also called
- ADCA3ADCAIIIautosomal dominant cerebellar ataxia type 3Pure cerebellar syndrome-mild pyramidal signs syndrome