|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A rare birth defect in women where the urethra and vagina both open into a common channel. (Human Phenotype Ontology, HP_0100779)|
|Downloads & Tools|
5 genes associated with the urogenital sinus anomaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.