Catecholaminergic Polymorphic Ventricular Tachycardia Type 3

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal recessive subtype of catecholaminergic polymorphic ventricular tachycardia caused by mutation(s) in the TECRL gene, encoding trans-2,3-enoyl-CoA reductase-like.

**Synonyms:** - CPVT3