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bn:08301291n
Noun Concept
EN
congenital merosin-deficient muscular dystrophy 1A  CMD1A  congenital merosin-deficient muscular dystrophy type 1A  congenital muscular dystrophy due to laminin alpha2 deficiency  Congenital muscular dystrophy type 1A
EN
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 Wikidata
Definitions
Relations
Sources
EN
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 Wikidata
IS A
disease
rare disease
genetic disease
congenital muscular dystrophy
autosomal recessive disease
GENETIC ASSOCIATION
LAMA2
HEALTH SPECIALTY
neurology
Wikidata
EN
congenital merosin-deficient muscular dystrophy 1A
Wikidata Alias
EN
CMD1A, congenital merosin-deficient muscular dystrophy type 1A, congenital muscular dystrophy due to laminin alpha2 deficiency, Congenital muscular dystrophy type 1A, MDC1A, merosin-deficient congenital muscular dystrophy type 1A, Merosin-negative congenital muscular dystrophy, Muscular Dystrophy, Congenital, Due to Partial Lama2 Deficiency, Muscular Dystrophy, Congenital Merosin-Deficient, MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A, MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A, Muscular Dystrophy, Congenital Merosin-Deficient, type 1A

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