congenital posterior urethral valve Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A developmental defect resulting in an obstructing membrane in the posterior male urethra. (Human Phenotype Ontology, HP_0010957)
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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.

Symbol Name
CHRM3 cholinergic receptor, muscarinic 3
H19 H19, imprinted maternally expressed transcript (non-protein coding)
SRCAP Snf2-related CREBBP activator protein