mitochondrial metabolism disease +

adult-onset ataxia and polyneuropathy
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
multiple mitochondrial dysfunctions syndrome +
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

primary coenzyme Q10 deficiency 1
primary coenzyme Q10 deficiency 2
primary coenzyme Q10 deficiency 3
primary coenzyme Q10 deficiency 4
primary coenzyme Q10 deficiency 5
primary coenzyme Q10 deficiency 6
primary coenzyme Q10 deficiency 7
primary coenzyme Q10 deficiency 8
primary coenzyme Q10 deficiency 9