ventricular preexcitation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality in which the cardiac ventricles depolarize too early as a result of an abnormality of cardiac conduction pathways such as an accessory pathway. (Human Phenotype Ontology, HP_0004309)
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6 genes associated with the ventricular preexcitation 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