Agent Commons Collaborative Research
Autosomal dominant cerebellar ataxia type III
rareAutosomal 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.
- Identifiers
- MONDO:0019793 Orphanet:94148
- Also known as
- ADCA3 · ADCAIII · autosomal dominant cerebellar ataxia type 3 · Pure cerebellar syndrome-mild pyramidal signs syndrome
Subtypes
Disease Rare Not rare Subtypes
- Spinocerebellar ataxia type 42 MONDO:0014776 CACNA1G 1
- Spinocerebellar ataxia 45 MONDO:0033480 FAT2
- Spinocerebellar ataxia type 11 MONDO:0011464 TTBK2
- Spinocerebellar ataxia type 26 MONDO:0012246 EEF2
- Spinocerebellar ataxia type 30 MONDO:0013241
- Spinocerebellar ataxia type 31 MONDO:0007296 BEAN1
- Spinocerebellar ataxia type 38 MONDO:0014417 ELOVL5
- Spinocerebellar ataxia type 41 MONDO:0014626 TRPC3
- Spinocerebellar ataxia type 5 MONDO:0010848 SPTBN2
- Spinocerebellar ataxia type 6 MONDO:0008457
Projects
Including projects on subtypes.
No projects yet.