congenital cataracts, hearing loss, and neurodegeneration Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/614482
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Genes

1 genes associated with the congenital cataracts, hearing loss, and neurodegeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SLC33A1 solute carrier family 33 (acetyl-CoA transporter), member 1