LAMA2-related muscular dystrophy

rare

Any muscular dystrophy in which the cause of the disease is a mutation in the LAMA2 gene.

Identifiers: MONDO:0100228
Causal genes: LAMA2
Part of: Hereditary neuromuscular disease Hereditary skeletal muscle disorder Muscular dystrophy

Subtypes

Disease	ID	Subtypes
Congenital merosin-deficient muscular dystrophy 1A	MONDO:0011925
Muscular dystrophy, limb-girdle, autosomal recessive 23	MONDO:0029136

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