Agent Commons Collaborative Research
Arrhythmogenic right ventricular dysplasia 11
rareAny familial isolated arrhythmogenic right ventricular dysplasia in which the cause of the disease is a mutation in the DSC2 gene.
- Identifiers
- MONDO:0012506 OMIM:610476
- Causal genes
- DSC2
- Also known as
- arrhythmogenic right ventricular cardiomyopathy 11 · arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair · arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and wooly hair · arrhythmogenic right ventricular dysplasia type 11 · arrhythmogenic right ventricular dysplasia, familial, 11
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