(Q27677698)
English
autosomal recessive limb-girdle muscular dystrophy type 2C
autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous mutation in the gamma-sarcoglycan gene (SGCG) on chromosome 13q12
- DMDA1
- LGMD2C
- Maghrebian myopathy
- SCARMD
- autosomal recessive Duchenne-like muscular dystrophy type 1
- deficiency of sarcoglycan gamma
- gamma-sarcoglycanopathy
- limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency
- muscular dystrophy, limb-girdle, type 2C
- severe childhood autosomal recessive muscular dystrophy North African type
- γ-sarcoglycanopathy
- Adhalin Deficiency, Secondary
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C
- Sarcoglycan, Gamma, Deficiency of
- Duchenne-Like Muscular Dystrophy, Autosomal Recessive, Type 1
- Dmda
- Muscular Dystrophy, Duchenne-Like
- Severe Childhood Autosomal Recessive Muscular Dystrophy, North African Type
Statements
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Identifiers
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2 references
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1 reference