abnormal hymen development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003538
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1 gene mutations causing the abnormal hymen development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
VANGL2 VANGL planar cell polarity protein 2