urethral atresia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Congenital anomaly characterized by closure or failure to develop an opening in the urethra. (Human Phenotype Ontology, HP_0000068)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000068
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2 genes associated with the urethral atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
WNT3 wingless-type MMTV integration site family, member 3
ZIC3 Zic family member 3