DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
Disease: Benign congenital myopathy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		0.200 Biomarker disease MGD mdxCv3 mouse is a model for electroretinography of Duchenne/Becker muscular dystrophy. 7843915 1995
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		0.200 Biomarker disease MGD Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice. 2919177 1989