| 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 |
| Similar Terms | |
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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 |