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
- CI
- chemically induced 3
- CL
- classification 7
- CO
- complications 14
- CN
- congenital 1
- DI
- diagnosis 58
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy 9
- EC
- economics
- EM
- embryology
- EN
- enzymology 12
- EP
- epidemiology 2
- EH
- ethnology
- ET
- etiology 10
- GE
- genetics 61
- HI
- history
- IM
- immunology 2
- ME
- metabolism 23
- MI
- microbiology 1
- MO
- mortality
- NU
- nursing 1
- PS
- parasitology
- PA
- pathology 13
- PP
- physiopathology 20
- PC
- prevention & control 6
- PX
- psychology 1
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 11
- UR
- urine 1
- VE
- veterinary
- VI
- virology
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency Disease MeSH Browser
Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of Disease MeSH Browser
Ataxia Neuropathy Spectrum Disease MeSH Browser
Ataxia and Polyneuropathy, Adult-Onset Disease MeSH Browser
Carnitine Palmitoyltransferase II Deficiency, Late-Onset Disease MeSH Browser
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal Disease MeSH Browser
Childhood Myocerebrohepatopathy Spectrum Disease MeSH Browser
Coenzyme Q10 Deficiency Disease MeSH Browser
Combined Oxidative Phosphorylation Deficiency 4 Disease MeSH Browser
Combined Oxidative Phosphorylation Deficiency 5 Disease MeSH Browser
Cowden-Like Syndrome Disease MeSH Browser
Deoxyguanosine Kinase Deficiency Disease MeSH Browser
Hypermetabolism due to Defect in Mitochondria Disease MeSH Browser
Hypomyelination, Global Cerebral Disease MeSH Browser
Hypotonia-Cystinuria Syndrome Disease MeSH Browser
Leukodystrophy, Hypomyelinating, 4 Disease MeSH Browser
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Disease MeSH Browser
Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency Disease MeSH Browser
Mitochondrial Complex II Deficiency Disease MeSH Browser
Mitochondrial Complex III Deficiency Disease MeSH Browser
Mitochondrial DNA Depletion Syndrome, Myopathic Form Disease MeSH Browser
Mitochondrial Phosphate Carrier Deficiency Disease MeSH Browser
Mitochondrial complex I deficiency Disease MeSH Browser
Multiple Mitochondrial Dysfunctions Syndrome Disease MeSH Browser
Myopathy with Giant Abnormal Mitochondria Disease MeSH Browser
Myopathy, Cataract, Hypogonadism Syndrome Disease MeSH Browser
Navajo neurohepatopathy Disease MeSH Browser
Noninsulin-dependent diabetes mellitus with deafness Disease MeSH Browser
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria Disease MeSH Browser
Parkinson Disease, Mitochondrial Disease MeSH Browser
Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial Disease MeSH Browser
Progressive External Ophthalmoplegia With Hypogonadism Disease MeSH Browser
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 Disease MeSH Browser
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 Disease MeSH Browser
Proximal Myopathy with Focal Depletion of Mitochondria Disease MeSH Browser
Sarcosinemia Disease MeSH Browser
Spinocerebellar Ataxia with Epilepsy Disease MeSH Browser
Succinate-Coa Ligase Deficiency Disease MeSH Browser
VDAC Deficiency Disease MeSH Browser
VLCAD deficiency Disease MeSH Browser
Wolfram Syndrome 2 Disease MeSH Browser
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