Paroxysmal Familial Ventricular Fibrillation-2

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant condition caused by mutation(s) in the DPP6 gene, encoding A-type potassium channel modulatory protein DPP6. It is characterized by paroxysms of ventricular fibrillation despite the absence of any structural cardiac anomalies.

**Synonyms:** - VF2