|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
2 genes/proteins associated with the disease Paroxysmal ventricular fibrillation from the curated CTD Gene-Disease Associations dataset.