mitochondrial metabolism disease +

adult-onset ataxia and polyneuropathy
coenzyme Q10 deficiency disease +
combined oxidative phosphorylation deficiency +
cytochrome-c oxidase deficiency disease +
deafness-dystonia-optic neuronopathy syndrome
ethylmalonic encephalopathy
GRACILE syndrome
mitochondrial complex I deficiency +
mitochondrial complex II deficiency
mitochondrial complex III deficiency +
mitochondrial complex V (ATP synthase) deficiency +
mitochondrial DNA depletion syndrome +
mitochondrial pyruvate carrier deficiency
mitochondrial short-chain enoyl-CoA hydratase 1 deficiency
NARP syndrome
neonatal severe encephalopathy with lactic acidosis and brain abnormalities
neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities
Pearson syndrome
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis

auditory neuropathy and optic atrophy
episodic mitochondrial myopathy with optic atrophy and reversible leukoencephalopathy
multiple mitochondrial dysfunctions syndrome 1
multiple mitochondrial dysfunctions syndrome 10
multiple mitochondrial dysfunctions syndrome 2
multiple mitochondrial dysfunctions syndrome 3
multiple mitochondrial dysfunctions syndrome 4
multiple mitochondrial dysfunctions syndrome 5
multiple mitochondrial dysfunctions syndrome 6
multiple mitochondrial dysfunctions syndrome 7
multiple mitochondrial dysfunctions syndrome 9B