wolff-parkinson-white syndrome Gene Set

Dataset HPO 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://compbio.charite.de/hpoweb/showterm?id=HP:0001716
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Genes

6 genes associated with the wolff-parkinson-white syndrome phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GAA glucosidase, alpha; acid
LAMP2 lysosomal-associated membrane protein 2
MTFMT mitochondrial methionyl-tRNA formyltransferase
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2