(Q24960548)
English
autosomal recessive limb-girdle muscular dystrophy type 2D
autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous or compound heterozygous mutation in the alpha-sarcoglycan gene (SGCA; 600119) on chromosome 17q
- DMDA2
- Duchenne-like autosomal recessive muscular dystrophy type 2
- LGMD2D
- muscular dystrophy, limb-girdle, type 2D
- primary adhalinopathy
- alpha-sarcoglycanopathy
- α-sarcoglycanopathy
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D
- Limb-Girdle Muscular Dystrophy Type 2D
- Adhalinopathy, Primary
- Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency
- Duchenne-Like Autosomal Recessive Muscular Dystrophy, Type 2
Statements
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C142081
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Identifiers
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