Catecholaminergic polymorphic ventricular tachycardia Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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://www.omim.org/entry/604772
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Genes

1 genes associated with the Catecholaminergic polymorphic ventricular tachycardia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
RYR2 ryanodine receptor 2 (cardiac)