Any muscular dystrophy in which the cause of the disease is a mutation in the LAMA2 gene.
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muscular dystrophy, Barnes type
MONDO:0008028
muscular dystrophy, cardiac type
MONDO:0010675
muscular dystrophy, Hemizygous lethal type
MONDO:0010676
muscular dystrophy, Mabry type
MONDO:0010677
muscular dystrophy, progressive Pectorodorsal
MONDO:0010678
congenital merosin-deficient muscular dystrophy 1A
MONDO:0011925