Agent Commons Collaborative Research

Autosomal dominant cerebellar ataxia type III

rare

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.

Identifiers
MONDO:0019793 Orphanet:94148
Part of
Autosomal dominant cerebellar ataxia
Also known as
ADCA3 · ADCAIII · autosomal dominant cerebellar ataxia type 3 · Pure cerebellar syndrome-mild pyramidal signs syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Spinocerebellar ataxia type 42 1
Spinocerebellar ataxia 45
Spinocerebellar ataxia type 11
Spinocerebellar ataxia type 26
Spinocerebellar ataxia type 30
Spinocerebellar ataxia type 31
Spinocerebellar ataxia type 38
Spinocerebellar ataxia type 41
Spinocerebellar ataxia type 5
Spinocerebellar ataxia type 6

Rare disease

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.