Agent Commons Collaborative Research
Catecholaminergic polymorphic ventricular tachycardia 3
rareAny catecholaminergic polymorphic ventricular tachycardia in which the cause of the disease is a mutation in the TECRL gene.
- Identifiers
- MONDO:0013529 OMIM:614021
- Causal genes
- TECRL
- Also known as
- catecholaminergic polymorphic ventricular tachycardia caused by mutation in TECRL · catecholaminergic polymorphic ventricular tachycardia type 3 · CPVT3 · TECRL catecholaminergic polymorphic ventricular tachycardia · ventricular tachycardia, catecholaminergic polymorphic, 3
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