Structured Summary
Abstract
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.
MeSH Record
Classification
Broader headings
Narrower headings
- Autosomal Dominant Optic Atrophy
- Carbamoyl-Phosphate Synthase I Deficiency Disease
- Cytochrome-c Oxidase Deficiency
- Friedreich Ataxia
- Hereditary Leber Optic Atrophy
- Leigh Disease
- Mitochondrial Myopathies
- Multiple Acyl Coenzyme A Dehydrogenase Deficiency
- Pyruvate Carboxylase Deficiency Disease
- Pyruvate Dehydrogenase Complex Deficiency Disease
Related Concepts
Knowledge Graph
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MeSH Record
Synonyms
22 entry terms
- Mitochondrial Disorders
- Disease, Mitochondrial
- Disorder, Mitochondrial
- Mitochondrial Disease
- Mitochondrial Disorder
- Electron Transport Chain Deficiencies, Mitochondrial
- Mitochondria Dysfunction
- Mitochondrial DNA Depletion Syndromes
- Mitochondrial Defect
- Mitochondrial Dysfunction
- Mitochondrial Electron Transport Chain Deficiencies
- Mitochondrial Respiratory Chain Deficiencies
- Oxidative Phosphorylation Deficiencies
- Respiratory Chain Deficiencies, Mitochondrial
- Defect, Mitochondrial
- Deficiency, Oxidative Phosphorylation
- Dysfunction, Mitochondria
- Dysfunction, Mitochondrial
- Mitochondria Dysfunctions
- Mitochondrial Dysfunctions
- Oxidative Phosphorylation Deficiency
- Phosphorylation Deficiency, Oxidative
MeSH Record
Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
general or unspecified; prefer specifics
MeSH Record
History Note
2002; use MITOCHONDRIAL MYOPATHIES 2000-2001
MeSH Record
Previous Indexing
- Mitochondria (1987-2001)
- Mitochondrial Myopathies (1992-2001)
MeSH Hierarchy
Tree Number
MeSH Record
NLM Classification
QU 260.5.M6
AMA Style
References
- National Library of Medicine. Mitochondrial Diseases. Medical Subject Headings (MeSH). 2026. Unique ID D028361. http://id.nlm.nih.gov/mesh/2026/D028361
- Mitochondrial Diseases. In: Wikipedia. https://en.wikipedia.org/wiki/Mitochondrial_disease
- Mitochondrial Diseases. In: Wikidata. https://www.wikidata.org/wiki/Q935710