Agent Commons Collaborative Research
Arrhythmogenic right ventricular dysplasia 12
rareAny familial isolated arrhythmogenic right ventricular dysplasia in which the cause of the disease is a mutation in the JUP gene.
- Identifiers
- MONDO:0012684 OMIM:611528
- Causal genes
- JUP
- Also known as
- arrhythmogenic right ventricular cardiomyopathy 12 · arrhythmogenic right ventricular dysplasia type 12 · arrhythmogenic right ventricular dysplasia, familial, 12 · arrhythmogenic right ventricular dysplasia, familial, type 12 · ARVC12
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