Catecholaminergic polymorphic ventricular tachycardia 1

Definition

Polymorphic ventricular tachycardia induced by adrenergic stress. It is inherited in an autosomal dominant pattern and is caused by mutations in the ryanodine receptor 2 (RYR2) gene.

Also known as arrhythmogenic right ventricular cardiomyopathy 2, arrhythmogenic right ventricular dysplasia 2, arrhythmogenic right ventricular dysplasia type 2, arrhythmogenic right ventricular dysplasia, familial, type 2, ARVC2, ARVD2, catecholaminergic polymorphic ventricular tachycardia 1, catecholaminergic polymorphic ventricular tachycardia type 1, familial arrhythmogenic right ventricular dysplasia 2, familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in RYR2, RYR2 familial isolated arrhythmogenic right ventricular dysplasia, ventricular tachycardia, catecholaminergic polymorphic, 1 — per MONDO

Also identified as

• DOID 0060675 per MONDO
• DOID 0110071 per MONDO
• MESH C563409 per MONDO
• NCIT C123414 per MONDO
• OMIM 600996 per MONDO
• OMIM 604772 per MONDO
• UMLS C1631597 per MONDO

Affected Organs