All diseases

OMIM ID
253700
OMIM term:
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C
Alternative terms:
MUSCULAR DYSTROPHY, DUCHENNE-LIKE
DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1
DMDA
ADHALIN DEFICIENCY, SECONDARY
SARCOGLYCAN, GAMMA, DEFICIENCY OF
SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICAN TYPE; SCARMD
MAGHREBIAN MYOPATHY
(∗) Location:
13q12.12  
(†) Associated OMIM genes:
SGCG  
(‡) Associated MGI genes:
Sgcg  

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