|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A disorder of the cardiac conduction system of the heart characterized by ventricular preexcitation due to the presence of an abnormal accessory atrioventricular electrical conduction pathway. (Human Phenotype Ontology, HP_0001716)|
|Downloads & Tools|
1 genes associated with the wolff-parkinson-white syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
|PRKAG2||protein kinase, AMP-activated, gamma 2 non-catalytic subunit|