uterus didelphys Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A malformation of the uterus in which the uterus is present as a paired organ as a result of the failure of fusion of the mullerian ducts during embryogenesis. (Human Phenotype Ontology, HP_0003762)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003762
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3 genes associated with the uterus didelphys phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AXIN1 axin 1
GATA3 GATA binding protein 3
HOXA13 homeobox A13