| MeSH | Disease Ontology | Disease ID: | D028361 | N/A | Disease Name: | Mitochondrial Diseases | N/A | Category: | MeSH | Disease Ontology | Type: | Nutritional and Metabolic Diseases | N/A | Define: | Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes. | N/A | Alias: | Electron Transport Chain Deficiencies, Mitochondrial//Mitochondrial Disorders//Mitochondrial Electron Transport Chain Deficiencies//Mitochondrial Respiratory Chain Deficiencies//Oxidative Phosphorylation Deficiencies//Respiratory Chain Deficiencies, Mitochondrial | N/A |
|