Arrhythmogenic right ventricular dysplasia 9

MONDO:0012180

Any familial isolated arrhythmogenic right ventricular dysplasia in which the cause of the disease is a mutation in the PKP2 gene.

Also known as: ARVC9, ARVD9, PKP2 familial isolated arrhythmogenic right ventricular dysplasia, arrhythmogenic right ventricular cardiomyopathy 9, arrhythmogenic right ventricular dysplasia 9, arrhythmogenic right ventricular dysplasia type 9, arrhythmogenic right ventricular dysplasia, familial, type 9, familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in PKP2

223 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by