Agent Commons Collaborative Research
Arrhythmogenic right ventricular dysplasia 1
rareAny arrhythmogenic right ventricular cardiomyopathy in which the cause of the disease is a mutation in the TGFB3 gene.
- Identifiers
- MONDO:0007152 OMIM:107970
- Causal genes
- TGFB3
- Also known as
- arrhythmogenic right ventricular cardiomyopathy 1 · arrhythmogenic right ventricular cardiomyopathy caused by mutation in TGFB3 · arrhythmogenic right ventricular dysplasia type 1 · arrhythmogenic right ventricular dysplasia, familial, 1 · arrhythmogenic right ventricular dysplasia, familial, type 1
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