List of diseases covered by
Dilated Cardiomyopathy NGS panel
| Gene | Condition |
| ABCC9 | Atrial fibrillation, familial, 12; Dilated cardiomyopathy 1O |
| ACTC1 | Atrial septal defect 5; Cardiomyopathy, dilated, 1R; Cardiomyopathy, hypertrophic, 11 |
| ACTN2 | Cardiomyopathy, dilated, 1AA, with or without LVNC |
| BAG3 | Cardiomyopathy, dilated, 1HH; Myopathy, myofibrillar, 6 |
| CSRP3 | Cardiomyopathy, dilated, 1M; Cardiomyopathy, hypertrophic, 12 |
| CRYAB | Cardiomyopathy, dilated, 1II; Cataract 16, multiple types; Myopathy, myofibrillar, 2; Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related |
| DES | Dilated cardiomyopathy 1I |
| DMD | Becker muscular dystrophy; Cardiomyopathy, dilated, 3B; Duchenne muscular dystrophy |
| DNAJC19 | 3-methylglutaconic aciduria, type V |
| DOLK | Congenital disorder of glycosylation, type Im |
| 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 |
| EMD | Emery-Dreifuss muscular dystrophy 1, X-linked |
| EYA4 | Cardiomyopathy, dilated, 1J; Deafness, autosomal dominant 10 |
| GATAD1 | Cardiomyopathy, dilated, 2B |
| JUP | Arrhythmogenic right ventricular cardiomyopathy, type 12; Naxos disease |
| LAMA4 | Cardiomyopathy, dilated, 1JJ |
| LAMP2 | Danon 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 |
| MYBPC3 | Cardiomyopathy, dilated, 1MM; Cardiomyopathy, hypertrophic, 4 |
| MYH6 | Atrial septal defect 3; Cardiomyopathy, dilated, 1EE; Cardiomyopathy, hypertrophic, 14 |
| MYH7 | Cardiomyopathy, dilated, 1S; Cardiomyopathy, hypertrophic, 1; Laing distal myopathy; Myopathy, myosin storage, autosomal dominant; Myopathy, myosin storage, autosomal recessive; Scapuloperoneal syndrome, myopathic type |
| MYPN | Cardiomyopathy, dilated, 1KK; Nemaline myopathy 11, autosomal recessive |
| NEXN | Cardiomyopathy, dilated, 1CC; Cardiomyopathy, hypertrophic, 20 |
| PKP2 | Arrhythmogenic right ventricular cardiomyopathy, type 9 |
| PLN | Dilated cardiomyopathy 1P; Familial hypertrophic cardiomyopathy 18 |
| RAF1 | Cardiomyopathy, dilated, 1NN; LEOPARD syndrome 2; Noonan syndrome 5 |
| RBM20 | Cardiomyopathy, dilated, 1DD |
| SCN5A | Atrial fibrillation, familial, 10; Brugada syndrome 1; Dilated cardiomyopathy 1E; Long QT syndrome 3; Sick sinus syndrome 1, autosomal recessive; Paroxysmal familial ventricular fibrillation 1 |
| SGCD | Cardiomyopathy, dilated, 1L; Muscular dystrophy, limb-girdle, type 2F |
| TAZ | Barth syndrome |
| TBX20 | Atrial septal defect 4 |
| TCAP | Cardiomyopathy, hypertrophic, 25; Muscular dystrophy, limb-girdle, type 2G |
| TNNC1 | Cardiomyopathy, dilated, 1Z; Cardiomyopathy, hypertrophic, 13 |
| TNNI3 | Cardiomyopathy, dilated, 2A; Cardiomyopathy, dilated, 1FF; Cardiomyopathy, familial restrictive, 1; Cardiomyopathy, hypertrophic, 7 |
| TNNT2 | Cardiomyopathy, dilated, 1D; Cardiomyopathy, familial restrictive, 3; Cardiomyopathy, hypertrophic, 2 |
| TPM1 | Cardiomyopathy, dilated, 1Y; Cardiomyopathy, hypertrophic, 3 |
| TTN | Cardiomyopathy, dilated, 1G; Cardiomyopathy, familial hypertrophic, 9; Muscular dystrophy, limb-girdle, type 2J; Myopathy, proximal, with early respiratory muscle involvement; Salih myopathy; Tibial muscular dystrophy, tardive |
| TTR | Amyloidosis, hereditary, transthyretin-related; Carpal tunnel syndrome, familial |
| VCL | Cardiomyopathy, dilated, 1W; Cardiomyopathy, hypertrophic, 15 |