spinocerebellar ataxia, autosomal recessive 16 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/615768
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Genes

1 genes associated with the spinocerebellar ataxia, autosomal recessive 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
STUB1 STIP1 homology and U-box containing protein 1, E3 ubiquitin protein ligase