arrhythmogenic right ventricular dysplasia 10 (Monarch Disease Ontology identifier MONDO_0012434) is any arrhythmogenic right ventricular cardiomyopathy in which the cause of the disease is a mutation in the DSG2 gene. Also known as: ARVC10, ARVD10, DSG2 arrhythmogenic right ventricular cardiomyopathy, 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, type 10, familial arrhythmogenic right ventricular dysplasia 10.