imperforate hymen Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A congenital disorder where the hymen (a membrane that surrounds or partially covers the external vaginal opening) does not have an opening and completely obstructs the vagina. (Human Phenotype Ontology, HP_0030011)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0030011
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Genes

1 genes associated with the imperforate hymen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
TBX3 T-box 3