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Summary Literature (0)
MIM:607346 - SPINOCEREBELLAR ATAXIA 19; SCA19

Xenbase Genes: kcnd3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011819 - spinocerebellar ataxia type 19/22

Disease Ontology (DO):
DOID:0050970 - spinocerebellar ataxia type 19/22