Protein
Gene Symbol
All allelic disease phenotypes - locus/disease symbols
SGCD (5q33-q34)
 | Muscular dystrophy, limb-girdle, type 2F -LGMD2F |
| Cardiomyopathy, dilated, 1L -CMD1L |
| Cardiomyopathy, dilated, 1L -CMD1L |
DES (2q35)
| Myopathy, desmin-related, cardioskeletal -DES |
| Cardiomyopathy, dilated, 1I -CMD1I |
DSC2 (18q12.1)
| Arrhythmogenic right ventricular dysplasia, 11 -ARVD11 |
DSG2 (18q12.1)
| Arrhythmogenic right ventricular dysplasia, 10 -ARVD10 |
DSP (6p24)
| Arrhythmogenic right ventricular dysplasia, 8 -ARVD8 |
DOK7 (4p16.2)
| Familial limb-girdle myasthenia -LGM |
DCTN1 (2p13)
| Neuronopathy, distal hereditary motor, type VIIB -HMN7B |
DNM2 (19p13.2)
| congenital muscular dystrophy with dynamin 2 defect - |
| Myopathy, centronuclear, autosomal dominant -CNM |
| dynamin2 related distal myopathy -CNM |
| Charcot-Marie-Tooth disease, dominant intermediate B -CMTDIB |
DYSF (2p12-14)
| Muscular dystrophy, limb-girdle, type 2B -LGMD2B |
| Miyoshi myopathy -MM |
| Myopathy, distal, with anterior tibial onset -DMAT |
DTNA (18q12)
| Left ventricular noncompaction, familial isolated -LVNC |
| Left ventricular noncompaction with congenital heart defects - |
DMD (Xp21.2)
| Becker muscular distrophy -BMD |
| Cardiomyopathy, dilated, X-linked -XLCM |
| Cardiomyopathy, Dilated, 3B -CMD3B |
| Duchenne muscular dystrophy -DMD |