(Q5811448)
(Redirected from Q32139651)
English
congenital merosin-deficient muscular dystrophy 1A
Congenital muscular dystrophy type 1A (MCD1A) belongs to a group of neuromuscular disorders with onset at birth or infancy characterized by hypotonia, muscle weakness and muscle wasting
- MDC1A
- Merosin-negative congenital muscular dystrophy
- congenital muscular dystrophy due to laminin alpha2 deficiency
- CMD1A
- merosin-deficient congenital muscular dystrophy type 1A
- Muscular Dystrophy, Congenital, Due to Partial Lama2 Deficiency
- congenital merosin-deficient muscular dystrophy type 1A
- MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
- Muscular Dystrophy, Congenital Merosin-Deficient, type 1A
- Congenital muscular dystrophy type 1A
- MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A
- Muscular Dystrophy, Congenital Merosin-Deficient
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C118783
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C118783
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