wolff-parkinson-white syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/194200
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Genes

1 genes associated with the wolff-parkinson-white syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit