|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Congenital anomaly characterized by closure or failure to develop an opening in the urethra. (Human Phenotype Ontology, HP_0000068)|
|Downloads & Tools|
2 genes associated with the urethral atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.