Cataract, congenital Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A congenital cataract. (Human Phenotype Ontology, HP_0000519)
External Link http://www.ncbi.nlm.nih.gov/medgen/?term=C0009691
Similar Terms
Downloads & Tools

Genes

1 genes associated with the Cataract, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
PITX3 paired-like homeodomain 3