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Metabolic myopathy

MONDO:0020123

A group of rare inherited disorders characterized by a deficiency of enzymes that are involved in metabolic pathways that affect muscles. The disorders are characterized by muscle dysfunction.

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

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Sub-types

Autosomal dominant mitochondrial myopathy with exercise intolerance (0) Endocrine myopathy (0) Hereditary myopathy with lactic acidosis due to ISCU deficiency (0) Metabolic myopathy due to lactate transporter defect (0)

Broader categories

Disease (618) Musculoskeletal system disorder (196) Muscle tissue disorder (53) Human disease (14) Myopathy (11) Skeletal muscle disorder (8) Disease by body system or component (0)
Trials to join now! 17 Not yet recruiting 6 Not yet finished but already full! 4 Completed 8 Terminated 1
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