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MIM:164500 - SPINOCEREBELLAR ATAXIA 7; SCA7
Xenbase Genes: atxn7
Human Disease Resource: OMIM
MONDO:0008120 - spinocerebellar ataxia type 7 |
MONDO:0016163 - autosomal dominant cerebellar ataxia type II |
DOID:0050958 - spinocerebellar ataxia type 7 |