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 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