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Inborn mitochondrial myopathy

MONDO:0009637

Myopathy caused by mitochondrial abnormalities.

Also known as: mitochondrial myopathy

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

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Sub-types

MELAS syndrome (12) Barth syndrome (4) Kearns-Sayre syndrome (4) MERRF syndrome (4) Mitochondrial encephalomyopathy (3) Mitochondrial neurogastrointestinal encephalomyopathy (3) Mitochondrial trifunctional protein deficiency (3) Myopathy, lactic acidosis, and sideroblastic anemia (3) Progressive external ophthalmoplegia (2) Adenosine monophosphate deaminase deficiency (1) MELAS syndrome caused by mutation in MTTL1 (1) Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2 (1) Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy (0) Autosomal dominant mitochondrial myopathy with exercise intolerance (0) Autosomal dominant progressive external ophthalmoplegia (0) Autosomal recessive progressive external ophthalmoplegia (0) Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 (0) Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 (0) Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3 (0) Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4 (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) Human disease (14) Myopathy (11)
Trials to join now! 58 Not yet recruiting 14 Not yet finished but already full! 19 Completed 21 Terminated 2
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