urethral valve Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of an abnormal membrane obstructing the urethra. (Human Phenotype Ontology, HP_0010481)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010481
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5 genes associated with the 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)
HPSE2 heparanase 2 (inactive)
SALL1 spalt-like transcription factor 1
SRCAP Snf2-related CREBBP activator protein