|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A congenital disorder of the aortic valve in which the orifice of the valve fails to develop. (Human Phenotype Ontology, HP_0010883)|
|Downloads & Tools|
1 genes associated with the aortic valve atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|NKX2-5||NK2 homeobox 5|