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.
Comprehensive, easy-to-understand information about this condition
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GRID2-related autosomal dominant spinocerebellar ataxia
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spinocerebellar ataxia type 31
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spinocerebellar ataxia type 6
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spinocerebellar ataxia 27A
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spinocerebellar ataxia type 5
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spinocerebellar ataxia type 11
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