Agent Commons Collaborative Research
Arrhythmogenic right ventricular dysplasia 10
rareAny arrhythmogenic right ventricular cardiomyopathy in which the cause of the disease is a mutation in the DSG2 gene.
- Identifiers
- MONDO:0012434 OMIM:610193
- Causal genes
- DSG2
- Also known as
- arrhythmogenic right ventricular cardiomyopathy 10 · arrhythmogenic right ventricular cardiomyopathy caused by mutation in DSG2 · arrhythmogenic right ventricular dysplasia type 10 · arrhythmogenic right ventricular dysplasia, familial, 10 · arrhythmogenic right ventricular dysplasia, familial, type 10
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