List of diseases covered by Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
NGS panel
| Gene | Condition |
| CTNNA3 | Arrhythmogenic right ventricular dysplasia, familial, 13 |
| DES | Dilated cardiomyopathy 1I |
| DSC2 | Arrhythmogenic right ventricular cardiomyopathy, type 11 |
| DSG2 | Arrhythmogenic right ventricular cardiomyopathy, type 10; Dilated cardiomyopathy 1BB |
| DSP | Arrhythmogenic right ventricular cardiomyopathy, type 8; Cardiomyopathy dilated with woolly hair and keratoderma; Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis |
| FLNC | Arrhythmogenic right ventricular dysplasia, familial; Cardiomyopathy, familial hypertrophic, 26; Cardiomyopathy, familial restrictive 5; Myopathy, distal, 4; Myopathy, myofibrillar, 5 |
| JUP | Arrhythmogenic right ventricular cardiomyopathy, type 12; Naxos disease |
| LDB3 | Cardiomyopathy, dilated, 1C, with or without LVNC; Myopathy, myofibrillar, 4 |
| LMNA | Muscular dystrophy, limb-girdle, type 1B; Charcot-Marie-Tooth disease, type 2B1; Cardiomyopathy, dilated, 1A; Emery-Dreifuss muscular dystrophy 2, AD; Emery-Dreifuss muscular dystrophy 3, AR; Muscular dystrophy, congenital |
| PKP2 | Arrhythmogenic right ventricular cardiomyopathy, type 9 |
| PLN | Dilated cardiomyopathy 1P; Familial hypertrophic cardiomyopathy 18 |
| RYR2 | Arrhythmogenic right ventricular dysplasia, familial, 2; Catecholaminergic polymorphic ventricular tachycardia type 1 |
| TGFB3 | Arrhythmogenic right ventricular dysplasia, familial 1 |
| TMEM43 | Arrhythmogenic right ventricular cardiomyopathy, type 5 |
| TTN | Muscular dystrophy, limb-girdle, type 2J; Myopathy, proximal, with early respiratory muscle involvement; Salih myopathy; Tibial muscular dystrophy, tardive; Cardiomyopathy, dilated, 1G; Cardiomyopathy, familial hypertrophic, 9 |