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LAMA2-related muscular dystrophy

MONDO:0100228

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

Also known as: LAMA2-related muscular dystrophy

41 clinical trials for this condition and its sub-types.

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Sub-types

Congenital merosin-deficient muscular dystrophy 1A (2) Muscular dystrophy, limb-girdle, autosomal recessive 23 (0)

Broader categories

Disease (618) Nervous system disorder (217) Musculoskeletal system disorder (196) Hereditary disease (172) Neuromuscular disease (98) Muscular dystrophy (68) Muscle tissue disorder (53) Human disease (14) Myopathy (11) Skeletal muscle disorder (8)
Trials to join now! 21 Not yet recruiting 8 Not yet finished but already full! 4 Completed 7 Terminated 1
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