|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||anomaly in the morphogenesis of the thin membrane which may partially occlude the opening of the vagina; often absent in normal females (Mammalian Phenotype Ontology, MP_0003538)|
|Downloads & Tools|
1 gene mutations causing the abnormal hymen development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|VANGL2||VANGL planar cell polarity protein 2|