Wolff-Parkinson-White Syndrome Gene Set

Dataset HuGE Navigator Gene-Phenotype 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)
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3 genes associated with the Wolff-Parkinson-White Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
DISC1 disrupted in schizophrenia 1
MT-ND5 NADH dehydrogenase, subunit 5 (complex I)