Protein | Gene Symbol | All allelic disease phenotypes - locus/disease symbols |
| delta-sarcoglycan | |  * Muscular dystrophy, limb-girdle, type 2F - LGMD2F (1.24, 10.38)
* Dilated Cardiomyopathy, 1L - CMD1L (1.24, 10.38)
|
desmin | | * Desmin-related myopathy - DRM (5.2, 10.35)
* Myofibrillar myopathy, desmin-related myopathy - (5.2, 10.35)
* Dilated cardiomyopathy, 1I - CMD1I (5.2, 10.35)
| desmocollin 2 | | * Arrhythmogenic right ventricular dysplasia, 11 - ARVD11 (10.82)
| desmoglein 2 | | * Arrhythmogenic right ventricular dysplasia, 10 - ARVD10 (10.81)
| desmoplakin | | * Arrhythmogenic right ventricular dysplasia, 8 - ARVD8 (10.79)
| DNA (cytosine-5)-methyltransferase 1 | | * Hereditary sensory neuropathy with dementia and hearing loss - (14.62)
* Neuropathy, hereditary sensory, type 1E - HSN1E (14.62)
| docking protein 7 | | * Familial limb-girdle myasthenia - LGM (11.15)
| double homeobox 4 | | * Muscular dystrophy, facioscapulohumeral - FSHD (1.9)
* Muscular dystrophy, facioscapulohumeral, type 1A - FSHD1A (1.9)
| dynactin 1 | | * Neuronopathy, distal hereditary motor, type VIIB - HMN7B (12.17)
| dynamin 2 | | * centronuclear myopathy, dominant - CNM (2.25, 3.15, 4.15, 14.12)
| dynein, cytoplasmic 1, heavy chain 1 | | * Charcot-Marie-Tooth disease, axonal, type 20 - CMT2O (14.49)
| dysferlin | | * Muscular dystrophy, limb-girdle, type 2B - LGMD2B (1.20, 4.1)
* Miyoshi myopathy - MM (1.20, 4.1)
| dystrobrevin, alpha | | * Left ventricular noncompaction, familial isolated - LVNC (10.70)
* Left ventricular noncompaction with congenital heart defects - (10.70)
| Dystroglycan1 (dystrophin-associated glycoprotein 1) | | * Muscular dystrophy-dystroglycanopathy (limb-girdle) - MDDGC7 (1.35)
| dystrophin | | * Becker muscular distrophy - BMD (1.1, 10.55)
* Cardiomyopathy, dilated, X-linked - XLCM (1.1, 10.55)
* Cardiomyopathy, Dilated, 3B - CMD3B (1.1, 10.55)
* Duchenne muscular dystrophy - DMD (1.1, 10.55)
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