BC65.5 Catecholaminergic polymorphic ventricular tachycardia
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe genetic arrhythmogenic disorder of childhood characterised by adrenergically-induced ventricular tachycardia (bidirectional ventricular tachycardia and, less frequently, supraventricular tachycardia and atrial fibrillation) manifesting as syncope and sudden death.
synonyms
- Catecholaminergic polymorphic ventricular tachycardia
- Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation
- Catecholaminergic polymorphic ventricular tachycardia due to Calsequestrin mutation
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