Mitochondrial Diseases
| Definition: |
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. |
| Notes: |
GEN or unspecified; prefer specifics |
| Also Called: |
Electron Transport Chain Deficiencies, Mitochondrial,Oxidative Phosphorylation Deficiencies,Respiratory Chain Deficiencies, Mitochondrial |
| Previously Indexed: |
Mitochondria (1987-2001),Mitochondrial Myopathies (1992-2001) |
Mitochondrial Diseases Definitions and Terms
MedicalGlossary.org is designed as a free, browsable resource for all. The medical terms and definitions are not intended to replace medical informaion provided by licensed healthcare professionals. Please see a doctor if you need medical assistance. Don't see the medical term you were researching? Send us an e-mail from our "about us" page. We will do our best to research and classify new medical terms in a timely manner. Our current list of medical terms is over 26,000. Data sources include the U.S. National Library of Medicine, 2004 Medical Subject Headings.
|