Details of Disease
General Information of Disease (ID: DISQBYEM)
| Disease Name | Autosomal dominant cerebellar ataxia type III | |||||
|---|---|---|---|---|---|---|
| Synonyms | Pure cerebellar syndrome-mild pyramidal signs syndrome; ADCA3; autosomal dominant cerebellar ataxia type 3; ADCAIII; autosomal dominant cerebellar ataxia type III | |||||
| 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.
|
|||||
| Disease Hierarchy | ||||||
| Disease Identifiers | ||||||