?cataract, congenital Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A congenital cataract. (Human Phenotype Ontology, HP_0000519)
Similar Terms
Downloads & Tools

Genes

1 genes associated with the ?cataract, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SORD sorbitol dehydrogenase