spinocerebellar ataxia 13 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/605259
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1 genes associated with the spinocerebellar ataxia 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
KCNC3 potassium channel, voltage gated Shaw related subfamily C, member 3