Mitochondrial Diseases [mitochondriální nemoci]
- Terms
-
deficit mitochondriálního elektronového transportního řetězce
mitochondriální dýchací řetězec - deficience
mitochondriopatie
oxidační fosforylace - deficience
poruchy mitochondriálního dýchacího řetězce
poruchy mitochondriálního elektronového transportního řetězce
poruchy oxidační fosforylace
-
Electron Transport Chain Deficiencies, Mitochondrial
Mitochondria Dysfunction
Mitochondrial Defect
Mitochondrial Disorders
Mitochondrial Dysfunction
Mitochondrial Electron Transport Chain Deficiencies
Mitochondrial Respiratory Chain Deficiencies
Oxidative Phosphorylation Deficiencies
Respiratory Chain Deficiencies, Mitochondrial
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.
- Annotation
- general or unspecified; prefer specifics
- DUI
- D028361 MeSH Browser
- CUI
- M0335637
- Previous indexing
- Mitochondria (1987-2001); Mitochondrial Myopathies (1992-2001)
- History note
- 2002; use MITOCHONDRIAL MYOPATHIES 2000-2001
- Public note
- 2002; see MITOCHONDRIAL MYOPATHIES 2000-2001
Allowable subheadings
- BL
- blood 4
- CF
- cerebrospinal fluid 0
- CI
- chemically induced 3
- CL
- classification 7
- CO
- complications 13
- CN
- congenital 1
- DI
- diagnosis 57
- DG
- diagnostic imaging 0
- DH
- diet therapy 0
- DT
- drug therapy 9
- EC
- economics 0
- EM
- embryology 0
- EN
- enzymology 12
- EP
- epidemiology 2
- EH
- ethnology 0
- ET
- etiology 10
- GE
- genetics 60
- HI
- history 0
- IM
- immunology 2
- ME
- metabolism 23
- MI
- microbiology 1
- MO
- mortality 0
- NU
- nursing 1
- PS
- parasitology 0
- PA
- pathology 13
- PP
- physiopathology 19
- PC
- prevention & control 6
- PX
- psychology 1
- RT
- radiotherapy 0
- RH
- rehabilitation 0
- SU
- surgery 0
- TH
- therapy 11
- UR
- urine 1
- VE
- veterinary 0
- VI
- virology 0
Narrower terms
- Carbamoyl-Phosphate Synthase I Deficiency Disease
- Cytochrome-c Oxidase Deficiency
- Friedreich Ataxia
- Leigh Disease
- Mitochondrial Myopathies
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency
- Optic Atrophy, Autosomal Dominant
- Optic Atrophy, Hereditary, Leber
- Pyruvate Carboxylase Deficiency Disease
- Pyruvate Dehydrogenase Complex Deficiency Disease