|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
3 genes associated with the uterus didelphys phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.