Arrhythmogenic right ventricular cardiomyopathy
MONDO:0016587Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disease that consists in progressive dystrophy of primarily the right ventricular myocardium with fibro-fatty replacement and ventricular dilation, and that is clinically characterized by ventricular arrhythmias and a risk of sudden cardiac death.
Also known as: ARVD, arrhythmogenic RVD, arrhythmogenic right ventricular cardiomyopathy, arrhythmogenic right ventricular dysplasia, right ventricular dysplasia
35 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Arrhythmogenic right ventricular dysplasia 9
(5)
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
(3)
Arrhythmogenic right ventricular dysplasia 1
(2)
Catecholaminergic polymorphic ventricular tachycardia 1
(1)
Arrhythmogenic right ventricular dysplasia 10
(0)
Arrhythmogenic right ventricular dysplasia 11
(0)
Arrhythmogenic right ventricular dysplasia 12
(0)
Arrhythmogenic right ventricular dysplasia 13
(0)
Arrhythmogenic right ventricular dysplasia 3
(0)
Arrhythmogenic right ventricular dysplasia 4
(0)
Arrhythmogenic right ventricular dysplasia 5
(0)
Arrhythmogenic right ventricular dysplasia 6
(0)
Arrhythmogenic right ventricular dysplasia 8
(0)
Arrhythmogenic right ventricular dysplasia, familial, 14
(0)
Familial isolated arrhythmogenic right ventricular dysplasia
(0)
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
(0)
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
(0)
Naxos disease
(0)