[diseases caused by abnormal function of the mitochondria; may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components; may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes. ( CSP )]
UMLS (CSP) C0751651mitochondrial disease/disorder
mitochondrial disorder
Relation/PAR: Metabolic Disease