?spinocerebellar ataxia, autosomal recessive 17 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/616127
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1 genes associated with the ?spinocerebellar ataxia, autosomal recessive 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CWF19L1 CWF19-like 1, cell cycle control (S. pombe)