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Up to: Inborn mitochondrial metabolism disorder · Congenital structural myopathy

Inborn mitochondrial myopathy

Myopathy caused by mitochondrial abnormalities.

18 trials tagged with this condition →

Mitochondrial encephalomyopathy 3 trials · 15 incl. sub-types Sub-types →
Progressive external ophthalmoplegia 4 trials · 8 incl. sub-types Sub-types →
Barth syndrome 5 trials
Mitochondrial neurogastrointestinal encephalomyopathy 4 trials Sub-types →
Mitochondrial trifunctional protein deficiency 3 trials Sub-types →
Myopathy, lactic acidosis, and sideroblastic anemia 3 trials Sub-types →
Adenosine monophosphate deaminase deficiency 1 trial
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis 1 trial Sub-types →
COX deficiency, benign infantile mitochondrial myopathy 0 trials
X-linked recessive mitochondrial myopathy 0 trials
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy 0 trials Sub-types →
Autosomal dominant mitochondrial myopathy with exercise intolerance 0 trials
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome 0 trials
Fatal infantile encephalocardiomyopathy 0 trials Sub-types →
Lethal infantile mitochondrial myopathy 0 trials
Maternally-inherited progressive external ophthalmoplegia 0 trials
Mitochondrial complex I deficiency, nuclear type 1 0 trials
Mitochondrial complex II deficiency, nuclear type 0 trials Sub-types →
Mitochondrial myopathy with a defect in mitochondrial-protein transport 0 trials
Mitochondrial myopathy with diabetes 0 trials
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency 0 trials
Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy 0 trials
Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome 0 trials
Mitochondrial myopathy-lactic acidosis-deafness syndrome 0 trials