aplasia/hypoplasia of the vagina Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Aplasia or developmental hypoplasia of the vagina. (Human Phenotype Ontology, HP_0011026)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011026
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Genes

5 genes associated with the aplasia/hypoplasia of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B3GALTL beta 1,3-galactosyltransferase-like
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
IRF6 interferon regulatory factor 6
PAX3 paired box 3
WNT4 wingless-type MMTV integration site family, member 4