Autosomal dominant cerebellar ataxia type III

MONDO:0019793

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.

Also known as: ADCA3, ADCAIII, Pure cerebellar syndrome-mild pyramidal signs syndrome, autosomal dominant cerebellar ataxia type 3, autosomal dominant cerebellar ataxia type III

28 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant cerebellar ataxia type III itself.

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↑ Autosomal dominant cerebellar ataxia (33)

Sub-types of Autosomal dominant cerebellar ataxia type III

Spinocerebellar ataxia type 6 9 trials
Spinocerebellar ataxia 45 0 trials
Spinocerebellar ataxia type 11 0 trials
Spinocerebellar ataxia type 26 0 trials
Spinocerebellar ataxia type 30 0 trials
Spinocerebellar ataxia type 31 0 trials
Spinocerebellar ataxia type 38 0 trials
Spinocerebellar ataxia type 41 0 trials
Spinocerebellar ataxia type 42 0 trials
1 sub-type
- Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits 0 trials
Spinocerebellar ataxia type 5 0 trials

Including sub-types (28) Tagged with Autosomal dominant cerebellar ataxia type III (0)

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