- OMIM ID
-
158900
- OMIM term:
- FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A
- Alternative terms:
-
MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1; FSHD1
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FMD
MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A
LANDOUZY-DEJERINE MUSCULAR DYSTROPHY FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED
FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS AND TORTUOSITY OF RETINAL ARTERIOLES, INCLUDED
- (∗) Location:
- 4q35
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
- Large
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