|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||.A ventricular septal defect that involves the inlet of the right ventricular septum immediately inferior to the AV valve apparatus. (Human Phenotype Ontology, HP_0011622)|
|Downloads & Tools|
1 genes associated with the inlet ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|GJA1||gap junction protein, alpha 1, 43kDa|