urogenital sinus anomaly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A rare birth defect in women where the urethra and vagina both open into a common channel. (Human Phenotype Ontology, HP_0100779)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100779
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5 genes associated with the urogenital sinus anomaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHRM3 cholinergic receptor, muscarinic 3
MKKS McKusick-Kaufman syndrome
SOX9 SRY (sex determining region Y)-box 9
SRD5A2 steroid-5-alpha-reductase, alpha polypeptide 2 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 2)
SRY sex determining region Y