All diseases

OMIM ID
608099
OMIM term:
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D
Alternative terms:
DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2
ADHALINOPATHY, PRIMARY
(∗) Location:
17q21.33  
(†) Associated OMIM genes:
SGCA  
(‡) Associated MGI genes:
Sgca  

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