Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 GeneticVariation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker HPO

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models. 12076680

2002
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Muscular dystrophy is frequently caused by disruption of the dystrophin-glycoprotein complex (DGC), which links muscle cells to the extracellular matrix. 12091319

2002
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Muscular dystrophies and the dystrophin-glycoprotein complex. 9146999

1997
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Dystrophin and muscular dystrophy: past, present, and future. 11592805

2001
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 GeneticVariation BEFREE Dystrophin gene mutations cause 2 common muscular dystrophies, Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD). 16246949

2005
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 AlteredExpression BEFREE Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human. 17826093

2007
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different ages. 1822792

1991
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Dystrophin is the gene product of the Duchenne (DMD) and Becker (BMD) muscular dystrophy gene locus on the short arm of the X chromosome. 1944822

1991
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 GeneticVariation BEFREE Dystrophin analysis in the differential diagnosis of autosomal recessive muscular dystrophy of childhood and Duchenne muscular dystrophy. 2206159

1990
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Dystrophin-deficient Duchenne cardiomyopathy is associated with Duchenne muscular dystrophy (DMD), the most common lethal muscular dystrophy. 22318092

2012
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Dystrophin-deficient muscular dystrophies (dystrophinopathies) are the most common form of muscular dystrophy, with variable clinical phenotypes ranging from the severe Duchenne (DMD) to the milder Becker (BMD) forms. 23790620

2013
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Dystrophin-related muscular dystrophies. 2571631

1989
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Dystrophin hydrophobic regions in the pathogenesis of Duchenne and Becker muscular dystrophies. 26042512

2015
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Dystrophin and the two related genetic diseases, Duchenne and Becker muscular dystrophies. 26295289

2015
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Dystrophin analysis in the diagnosis of muscular dystrophy. 2684033

1989
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Dystrophin/utrophin double-knockout (dKO) mice develop a more severe and progressive muscular dystrophy than the mdx mice, the most common murine model of Duchenne muscular dystrophy (DMD). 29078808

2017
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 GeneticVariation BEFREE Dystrophin gene deletions account for up to 68% of all Duchenne (DMD) and Becker (BMD) muscular dystrophy mutations. 7510932

1993
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Dystrophin, the protein product of the Duchenne muscular dystrophy (DMD) gene, was studied in 19 patients with Xp21 disorders and in 25 individuals with non-Xp21 muscular dystrophy. 8429320

1993
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Dystrophin-associated proteins and the muscular dystrophies. 9046976

1997
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 Biomarker BEFREE Dystrophin is bound to a complex of proteins in the muscle membrane, and primary abnormalities of these proteins have now been identified as the cause of some autosomally inherited forms of muscular dystrophy. 9259292

1997
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 GeneticVariation BEFREE A <i>De novo</i> Mutation in Dystrophin Causing Muscular Dystrophy in a Female Patient. 28937030

2017
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 GeneticVariation BEFREE A Japanese family with two types of muscular dystrophy: DNA analysis and the dystrophin test. 1875028

1991
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.500 GeneticVariation BEFREE A large variety of mutations in the dystrophin gene cause Duchenne and Becker muscular dystrophies, diseases affecting predominantly the striated muscles (skeletal and cardiac). 23116935

2013