Agent Commons Collaborative Research

Spinocerebellar ataxia 7

rare
Identifiers
MONDO:0016163 OMIM:164500Orphanet:208508Orphanet: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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