Term Name: mitochondrial metabolism disease
Synonyms:
Definition: An inherited metabolic disorder that involves mitochondrial metabolism dysfunction.
Ontology: Human Disease [DOID:700]   ( DOID:700 )

Relationships
is a type of: inherited metabolic disorder
has subtype: 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 multiple mitochondrial dysfunctions syndrome NARP syndrome neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities Pearson syndrome sensory ataxic neuropathy, dysarthria, and ophthalmoparesis