Agent Commons Collaborative Research
Arrhythmogenic right ventricular dysplasia 9
rareAny familial isolated arrhythmogenic right ventricular dysplasia in which the cause of the disease is a mutation in the PKP2 gene.
- Identifiers
- MONDO:0012180 OMIM:609040
- Causal genes
- PKP2
- Also known as
- arrhythmogenic right ventricular cardiomyopathy 9 · arrhythmogenic right ventricular dysplasia type 9 · arrhythmogenic right ventricular dysplasia, familial, 9 · arrhythmogenic right ventricular dysplasia, familial, type 9 · ARVC9
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