Inborn mitochondrial myopathy
MONDO:0009637Myopathy caused by mitochondrial abnormalities.
Also known as: mitochondrial myopathy
54 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
MELAS syndrome
(13)
Barth syndrome
(5)
Kearns-Sayre syndrome
(5)
MERRF syndrome
(5)
Mitochondrial neurogastrointestinal encephalomyopathy
(4)
Mitochondrial encephalomyopathy
(3)
Mitochondrial trifunctional protein deficiency
(3)
Myopathy, lactic acidosis, and sideroblastic anemia
(3)
Progressive external ophthalmoplegia
(3)
Adenosine monophosphate deaminase deficiency
(1)
Autosomal dominant progressive external ophthalmoplegia
(1)
MELAS syndrome caused by mutation in MTTL1
(1)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2
(1)
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
(1)
Spinocerebellar ataxia with epilepsy
(1)
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
(0)
Autosomal dominant mitochondrial myopathy with exercise intolerance
(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)