rs1057518962, DMD

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
EMG: myopathic abnormalities
CUI: C4021726
Disease: EMG: myopathic abnormalities
0.700 CausalMutation CLINVAR
Motor delay
CUI: C1854301
Disease: Motor delay
0.700 CausalMutation CLINVAR
Electromyogram abnormal
CUI: C0476403
Disease: Electromyogram abnormal
0.700 CausalMutation CLINVAR
Calf muscle hypertrophy
CUI: C1843057
Disease: Calf muscle hypertrophy
0.700 CausalMutation CLINVAR
Spasm
CUI: C0037763
Disease: Spasm
0.700 CausalMutation CLINVAR
Muscle Weakness
CUI: C0151786
Disease: Muscle Weakness
0.700 CausalMutation CLINVAR