Paroxysmal ventricular fibrillation Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe genetic arrhythmogenic disorder characterized by adrenergically induced ventricular tachycardia (VT) manifesting as syncope and sudden death. (Orphanet Rare Disease Ontology, Orphanet_3286)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537182
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Genes

2 genes/proteins associated with the disease Paroxysmal ventricular fibrillation from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SCN5A sodium channel, voltage gated, type V alpha subunit 2.88009
DPP6 dipeptidyl-peptidase 6 2.88009