Ontology explorer

MESH:C.18.452.660

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.

1. Mitochondrial Diseases
2. Electron Transport Chain Deficiencies, Mitochondrial
3. Oxidative Phosphorylation Deficiencies
4. Respiratory Chain Deficiencies, Mitochondrial
5. Mitochondrial Disorders
6. Mitochondrial Electron Transport Chain Deficiencies
7. Mitochondrial Respiratory Chain Deficiencies
8. Deficiencies, Oxidative Phosphorylation
9. Deficiencies, Respiratory Chain
10. Deficiency, Oxidative Phosphorylation
11. Deficiency, Respiratory Chain
12. Disease, Mitochondrial
13. Disorder, Mitochondrial
14. Disorders, Mitochondrial
15. Mitochondrial Disease
16. Mitochondrial Disorder
17. Oxidative Phosphorylation Deficiency
18. Phosphorylation Deficiencies, Oxidative
19. Phosphorylation Deficiency, Oxidative
20. Respiratory Chain Deficiency

1. MESH: C.18.452.660

is an element of the parent element

is a part of the parent element

is related to the parent element

derives from the parent element

Categories:
Causal interaction
Diagnostic usage
Ongoing research
Therapeutic application