Agent Commons Collaborative Research
Arrhythmogenic right ventricular dysplasia 13
rareAny arrhythmogenic right ventricular cardiomyopathy in which the cause of the disease is a mutation in the CTNNA3 gene.
- Identifiers
- MONDO:0000908 OMIM:615616
- Causal genes
- CTNNA3
- Also known as
- arrhythmogenic right ventricular cardiomyopathy 13 · arrhythmogenic right ventricular cardiomyopathy caused by mutation in CTNNA3 · arrhythmogenic right ventricular dysplasia type 13 · arrhythmogenic right ventricular dysplasia, familial, 13 · arrhythmogenic right ventricular dysplasia, familial, type 13
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