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bn:08301291n
Noun Concept
SYL
No term available
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
Relations
Sources
IS A
EN
disease
EN
rare disease
EN
genetic disease
EN
congenital muscular dystrophy
EN
autosomal recessive disease
GENETIC ASSOCIATION
EN
LAMA2
HEALTH SPECIALTY
EN
neurology

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