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Summary Literature (0)
MIM:164500 - SPINOCEREBELLAR ATAXIA 7; SCA7

Xenbase Genes: atxn7

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008120 - spinocerebellar ataxia type 7
MONDO:0016163 - autosomal dominant cerebellar ataxia type II

Disease Ontology (DO):
DOID:0050958 - spinocerebellar ataxia type 7