Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		0.700 CausalMutation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		0.700 GeneticVariation CLINVAR

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: C0151786
Disease: Muscle Weakness
Muscle Weakness 		0.500 CausalMutation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026848
Disease: Myopathy
Myopathy 		0.200 GeneticVariation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0026848
Disease: Myopathy
Myopathy 		0.200 CausalMutation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1850830
Disease: Exercise-induced myalgia
Exercise-induced myalgia 		0.110 GeneticVariation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		0.100 GeneticVariation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0015300
Disease: Exophthalmos
Exophthalmos 		0.100 GeneticVariation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		0.100 GeneticVariation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		0.100 CausalMutation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0037763
Disease: Spasm
Spasm 		0.100 CausalMutation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0234182
Disease: Gowers sign
Gowers sign 		0.100 GeneticVariation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0240421
Disease: Progressive muscle weakness
Progressive muscle weakness 		0.100 CausalMutation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		0.100 CausalMutation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		0.100 GeneticVariation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0349588
Disease: Short stature
Short stature 		0.100 GeneticVariation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal 		0.100 CausalMutation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C0850703
Disease: Frequent falls
Frequent falls 		0.100 GeneticVariation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1836156
Disease: Progressive proximal muscle weakness
Progressive proximal muscle weakness 		0.100 GeneticVariation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1836296
Disease: Muscle Weakness Lower Limb
Muscle Weakness Lower Limb 		0.100 GeneticVariation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1843057
Disease: Calf muscle hypertrophy
Calf muscle hypertrophy 		0.100 CausalMutation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1843057
Disease: Calf muscle hypertrophy
Calf muscle hypertrophy 		0.100 GeneticVariation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1844806
Disease: Weight less than 3rd percentile
Weight less than 3rd percentile 		0.100 GeneticVariation CLINVAR

Entrez Id: 1756
Gene Symbol: DMD
DMD
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger 		0.100 GeneticVariation CLINVAR