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OMIM:310200 - MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
DOID:11723 - Duchenne muscular dystrophy |
MONDO:0010679 - Duchenne muscular dystrophy |
Human Disease Resources: OMIM
Xenbase Genes: dmd.2, dmd.3, dmd.1, myf6
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DOID:11723 - Duchenne muscular dystrophy |
MONDO:0010679 - Duchenne muscular dystrophy |