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Diseases / Disease of genetic or genomic mechanism/ Hereditary disease/ Hereditary dementia/ Autosomal dominant cerebellar ataxia

Spinocerebellar ataxia 7

rare

Identifiers: MONDO:0016163 OMIM:164500 Orphanet:208508 Orphanet:94147
Causal genes: ATXN7
Part of: Autosomal dominant cerebellar ataxia
Also known as: ADCA, type II · ADCA2 · ADCAII · ataxia with pigmentary retinopathy · ATXN7 autosomal dominant cerebellar ataxia type II

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