|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A congenital defect with failure to open of the mitral valve orifice. (Human Phenotype Ontology, HP_0011560)|
|Downloads & Tools|
1 genes associated with the mitral atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|NKX2-5||NK2 homeobox 5|