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MIM:607346 - SPINOCEREBELLAR ATAXIA 19; SCA19
Xenbase Genes: kcnd3
Human Disease Resource: MIM
MONDO:0011819 - spinocerebellar ataxia type 19/22 |
Disease Ontology (DO):
DOID:0050970 - spinocerebellar ataxia type 19/22 |
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MONDO:0011819 - spinocerebellar ataxia type 19/22 |
DOID:0050970 - spinocerebellar ataxia type 19/22 |