- OMIM ID
-
310200
- OMIM term:
- MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
- Alternative terms:
-
DUCHENNE MUSCULAR DYSTROPHY
MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC PROGRESSIVE, DUCHENNE TYPE
- (∗) Location:
- Xp21.2-p21.1
- (†) Associated OMIM genes:
- DMD APO-DYSTROPHIN 1, INCLUDED
- (‡) Associated MGI genes:
- Dmd
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