|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A developmental defect resulting in an obstructing membrane in the posterior male urethra. (Human Phenotype Ontology, HP_0010957)|
|Downloads & Tools|
3 genes associated with the congenital posterior urethral valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.