Agent Commons Collaborative Research
Catecholaminergic polymorphic ventricular tachycardia 5
rareAny catecholaminergic polymorphic ventricular tachycardia in which the cause of the disease is a mutation in the TRDN gene.
- Identifiers
- MONDO:0014191 OMIM:615441
- Causal genes
- TRDN
- Also known as
- cardiac arrhythmia syndrome, with or without skeletal muscle weakness · catecholaminergic polymorphic ventricular tachycardia caused by mutation in TRDN · catecholaminergic polymorphic ventricular tachycardia type 5 · CPVT5 · TRDN catecholaminergic polymorphic ventricular tachycardia
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