191
|
|
|
Desmoglein 1 |
CDHF4, DG1, DSG, EPKHE, EPKHIA, PPKS1, SPPK1 |
Bicuspid aortic valve, Dermatitis, Dermatitis-multiple allergies-metabolic wasting syndrome, Diffuse palmoplantar hyperkeratosis, Diffuse palmoplantar keratoderma with painful fissures, Exfoliative dermatitis, Focal palmoplantar keratoderma with joint keratoses, Hypotrichosis, Keratosis palmoplantaris striata, Metabolic diseases, Palmoplantar keratoderma, Palmoplantar keratosis, Psoriasiform eczema, Striate palmoplantar keratoderma |
192
|
|
|
Desmoglein 2 |
CDHF5, HDGC |
Alzheimer disease, Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Hearing loss, Hypertrophic cardiomyopathy, Lipoatrophy, Lipodystrophy, Myopathy, Palmoplantar keratoderma, Ventricular cardiomyopathy, Ventricular tachycardia |
193
|
|
|
Desmoplakin |
DCWHKTA, DP |
Alopecia, Alveolitis, Anonychia, Aplasia cutis congenita, Arrhythmogenic right ventricular cardiomyopathy, Bicuspid aortic valve, Bronchiectasis, Cardiomyopathy, Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis, Cardiovascular abnormalities, Carvajal syndrome, Chronic obstructive pulmonary disease, Clinodactyly, Congestive heart failure, Dermatitis, Dermatitis-multiple allergies-metabolic wasting syndrome, Diffuse interstitial pulmonary fibrosis, Dilated cardiomyopathy with woolly hair and keratoderma, Ectodermal dysplasia, Epidermolysis bullosa, Erythrokeratodermia-cardiomyopathy syndrome, Gastroesophageal reflux disease, Gingival recession, Heart failure, Hereditary bundle branch system defect, Honeycomb lung, Hyperkeratosis, epidermolytic, Hypertrophic cardiomyopathy, Keratosis palmoplantaris striata, Lethal acantholytic erosive disorder, Long qt syndrome, Lung diseases, Nail diseases, Nail dysplasia, Nail dystrophy, Palmoplantar keratoderma, Parakeratosis, Patchy palmoplantar keratoderma, Pulmonary fibrosis, Hamman-rich syndrome, Skin erosion, Skin fragility-woolly hair syndrome, Palmoplantar keratoderma and woolly hair, Striate palmoplantar keratoderma, Syndactyly, Ulcer of esophagus, Ventricular arrhythmia, Ventricular cardiomyopathy, Ventricular fibrillation, Ventricular tachycardiaView all (35 more) |
194
|
|
|
Dentin sialophosphoprotein |
DFNA39, DGI1, DMP3, DPP, DSP |
Carcinoma, Deafness with dentinogenesis imperfecta, Deafness,nonsyndromic sensorineural, with dentinogenesis imperfecta, Dental pulp stone, Denticles, Dentin dysplasia, Dentinogenesis imperfecta, Hearing loss, Hereditary opalescent dentin, Mouth neoplasms, Malignant neoplasm of mouth, Opalescent dentin, Sensorineural hearing loss |
195
|
|
|
Dystrobrevin alpha |
D18S892E, DRP3, DTN, DTN-A, LVNC1, MMCKR2 |
Atrial fibrillation, Cardiomyopathy, Congestive heart failure, Hypoplastic left heart syndrome, Left ventricular hypertrophy, Left ventricular noncompaction, Meniere disease, Noncompaction cardiomyopathy, Patent ductus arteriosus, Ventricular arrhythmia, Ventricular septal defect |
196
|
|
|
Dystrobrevin beta |
- |
|
197
|
|
|
Deltex E3 ubiquitin ligase 1 |
RNF140, hDx-1 |
|
198
|
|
|
Dual specificity phosphatase 1 |
CL100, HVH1, MKP-1, MKP1, PTPN10 |
Arthritis, Dermatitis, Endometrioma, Endometriosis, Juvenile arthritis, Mental depression, Myocardial ischemia, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Still disease |
199
|
|
|
Dual specificity phosphatase 2 |
PAC-1, PAC1 |
|
200
|
|
|
Dual specificity phosphatase 3 |
VHR |
|