absent vas deferens Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Aplasia (congenital absence) of the vas deferens. (Human Phenotype Ontology, HP_0012873)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012873
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1 genes associated with the absent vas deferens phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AR androgen receptor