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OMIM:607346 - SPINOCEREBELLAR ATAXIA 19; SCA19
DOID:0050970 - spinocerebellar ataxia type 19/22 |
MONDO:0011819 - spinocerebellar ataxia type 19/22 |
Human Disease Resources: OMIM
Xenbase Genes: kcnd3
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DOID:0050970 - spinocerebellar ataxia type 19/22 |
MONDO:0011819 - spinocerebellar ataxia type 19/22 |