List of diseases covered by
Left Ventricular Noncompaction Cardiomyopathy
NGS panel
| Gene | Condition |
| ACTC1 | Left ventricular noncompaction 4; Cardiomyopathy, hypertrophic, 11; Atrial septal defect 5 |
| CASQ2 | Ventricular tachycardia, catecholaminergic polymorphic, 2 |
| DTNA | Left ventricular noncompaction 1, with or without congenital heart defects |
| FLNC | Arrhythmogenic right ventricular dysplasia, familial; Cardiomyopathy, familial hypertrophic, 26; Cardiomyopathy, familial restrictive 5; Myopathy, distal, 4; Myopathy, myofibrillar, 5 |
| LDB3 | Left ventricular noncompaction 3; 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; Heart-hand syndrome, Slovenian type; Lipodystrophy, familial partial, type 2; Malouf syndrome |
| MIB1 | Left ventricular noncompaction 7 |
| MYBPC3 | Left ventricular noncompaction 10; Cardiomyopathy, hypertrophic, 4 |
| MYH7 | Left ventricular noncompaction 5; Cardiomyopathy, hypertrophic, 1; Laing distal myopathy; Myopathy, myosin storage, autosomal dominant; Myopathy, myosin storage, autosomal recessive; Scapuloperoneal syndrome, myopathic type |
| PRDM16 | Left ventricular noncompaction 8 |
| TAZ | Barth syndrome |
| TNNT2 | Left ventricular noncompaction 6; Cardiomyopathy, familial restrictive, 3; Cardiomyopathy, hypertrophic, 2 |
| TPM1 | Left ventricular noncompaction 9; Cardiomyopathy, hypertrophic, 3 |
| VCL | Cardiomyopathy, dilated, 1W; Cardiomyopathy, hypertrophic, 15 |