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Mitochondrial encephalomyopathy

MONDO:0004675

A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5)

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

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Sub-types

MELAS syndrome (12) MERRF syndrome (4) MELAS syndrome caused by mutation in MTTL1 (1) MELAS syndrome caused by mutation in MTND1 (0) MELAS syndrome caused by mutation in MTND5 (0) MELAS syndrome caused by mutation in MTND6 (0) MELAS syndrome caused by mutation in MTTC (0) MELAS syndrome caused by mutation in MTTH (0) MELAS syndrome caused by mutation in MTTK (0) MELAS syndrome caused by mutation in MTTQ (0) MELAS syndrome caused by mutation in MTTS1 (0) MELAS syndrome caused by mutation in MTTS2 (0)

Broader categories

Disease (618) Metabolic disease (215) Musculoskeletal system disorder (196) Hereditary disease (172) Inborn mitochondrial metabolism disorder (57) Muscle tissue disorder (53) Inborn errors of metabolism (42) Mitochondrial disease (39) Inborn mitochondrial myopathy (15) Human disease (14)
Trials to join now! 43 Not yet recruiting 12 Not yet finished but already full! 14 Completed 16 Terminated 2
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