polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/612674
Similar Terms
Downloads & Tools

Genes

1 genes associated with the polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ABHD12 abhydrolase domain containing 12