deafness, cataract, retinitis pigmentosa, and sperm abnormalities Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/300719
Similar Terms
Downloads & Tools

Genes

1 genes associated with the deafness, cataract, retinitis pigmentosa, and sperm abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
DFCTRPS Deafness, cataract, retinitis pigmentosa, and sperm abnormalities