Other diseases that are caused by mutations to the RyR2 channel include arrhythmogenic right ventricular dysplasia, type 2 (ARVC/D2) [81,82,83,84], polymorphic ventricular tachycardia (PVT) [85,86], sudden infant death syndrome (SIDS) [87], sudden cardiac death (SCD) [88,89,90,91,92], and left ventricular non-compaction (LVNC) [93,94,95,96]. The gene discussed is RYR2; the disease is catecholaminergic polymorphic ventricular tachycardia 1.