Catecholaminergic polymorphic ventricular tachycardia 5

Definition

Any catecholaminergic polymorphic ventricular tachycardia in which the cause of the disease is a mutation in the TRDN gene.

Also known as cardiac arrhythmia syndrome, with or without skeletal muscle weakness, catecholaminergic polymorphic ventricular tachycardia 5, catecholaminergic polymorphic ventricular tachycardia caused by mutation in TRDN, catecholaminergic polymorphic ventricular tachycardia type 5, TRDN catecholaminergic polymorphic ventricular tachycardia — per MONDO

Also identified as

• DOID 0060679 per MONDO
• OMIM 615441 per MONDO
• UMLS C3809536 per MONDO