Table 1.

Inherited arrhythmogenic disorders

Mutations in genes encoding developmental components of the heart

Hypertrophic cardiomyopathy (HCM)

Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C)

Dilated cardiomyopathy (DC)

Mutations in genes encoding functional units of ion channels and/or transporter-associated proteins (“ion channelopathies”)

Congenital long-QT syndrome (LQTS)

Brugada syndrome (BrS)

Catecholaminergic polymorphic ventricular tachycardia (CPVT)

Short-QT syndrome (SQTS)