3811
|
|
|
Desmoglein 2 |
CDHF5, HDGC |
Alzheimer disease, Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Cardiac arrest, Cardiomyopathy, Dilated cardiomyopathy, Conduction disorder of the heart, Arrhythmogenic right ventricular dysplasia, Hypertrophic cardiomyopathy, Intellectual developmental disorder, Left ventricular noncompaction cardiomyopathy, Long qt syndrome, Ventricular fibrillation, Catecholaminergic polymorphic ventricular tachycardia |
3812
|
|
|
Desmoglein 3 |
ABOLM, CDHF6, PVA |
|
3813
|
|
|
Desmoglein 4 |
CDGF13, CDHF13, HYPT6, LAH |
|
3814
|
|
|
Desmoplakin |
DCWHKTA, DP |
Amyloidosis, Arrhythmogenic right ventricular cardiomyopathy, Bicuspid aortic valve, Brugada syndrome, Cardiac arrest, Cardiac arrhythmia, Cardiomyopathy, Dilated cardiomyopathy, Carvajal syndrome, Obstructive airway disease, Obstructive pulmonary disease, Conduction disorder of the heart, Ectodermal dysplasia, Junctional epidermolysis bullosa, Erythrokeratodermia-cardiomyopathy syndrome, Arrhythmogenic right ventricular dysplasia, Restrictive cardiomyopathy, Global developmental delay, Hereditary bundle branch system defect, Hypertrophic cardiomyopathy, Idiopathic pulmonary fibrosis, Interstitial lung disease, Keratosis palmoplantaris striata, Left ventricular disease, Left ventricular noncompaction cardiomyopathy, Lethal acantholytic epidermolysis bullosa, Long qt syndrome, Lung cancer, Migraine, Myocarditis, Paroxysmal familial ventricular fibrillation, Chronic obstructive pulmonary disease, Pulmonary fibrosis, Respiratory system disease, Right ventricular cardiomyopathy, Squamous cell carcinoma, Ventricular arrhythmia, Ventricular fibrillation, Catecholaminergic polymorphic ventricular tachycardia, Wolff-parkinson-white syndromeView all (25 more) |
3815
|
|
|
Dentin sialophosphoprotein |
DFNA39, DGI1, DMP3, DPP, DSP |
|
3816
|
|
|
Dystonin |
BP240, BPA, BPAG1, CATX-15, CATX15, D6S1101, DMH, DT, EBS3, EBSB2, HSAN6, MACF2 |
Alzheimer disease, Atrial fibrillation, Autism, Cardiomyopathy, Charcot-marie-tooth disease, Congenital joint contractures, Distal spinal muscular atrophy, Dominantly inherited sensory neuropathy, Epidermolysis bullosa, Esophageal atresia, Global developmental delay, Gout, Hereditary sensory and autonomic neuropathy, Moyamoya angiopathy, Multiple sclerosis, Open angle glaucoma, Pancreatic cancer, SchizophreniaView all (3 more) |
3817
|
|
|
Destrin, actin depolymerizing factor |
ACTDP, ADF, HEL32, bA462D18.2 |
|
3818
|
|
|
DSTN pseudogene 4 |
- |
|
3819
|
|
|
Dual serine/threonine and tyrosine protein kinase |
CAKUT1, DustyPK, HDCMD38P, RHDNS1, RIP5, RIPK5, SPG23 |
Spastic paraplegia, Basal cell carcinoma, Kidney disease, Obstructive pulmonary disease, Colorectal cancer, Hereditary spastic paraplegia, Congenital anomalies of kidney and urinary tract, Coronary artery disease, Melanoma, Dupuytren contracture, Metabolic syndrome, Obesity, Diabetes mellitus type 2 |
3820
|
|
|
D-aminoacyl-tRNA deacylase 1 |
C20orf88, DTD, DUE-B, DUEB, HARS2, pqn-68 |
|
