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Mitochondrial Diseases MeSH Descriptor Data 2022


MeSH Heading
Mitochondrial Diseases
Tree Number(s)
C18.452.660
Unique ID
D028361
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D028361
Annotation
general or unspecified; prefer specifics
Scope Note
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.
Entry Version
MITOCHONDRIAL DIS
Entry Term(s)
Electron Transport Chain Deficiencies, Mitochondrial
Mitochondrial Disorders
Mitochondrial Electron Transport Chain Deficiencies
Mitochondrial Respiratory Chain Deficiencies
Oxidative Phosphorylation Deficiencies
Respiratory Chain Deficiencies, Mitochondrial
NLM Classification #
QU 260.5.M6
Previous Indexing
Mitochondria (1987-2001)
Mitochondrial Myopathies (1992-2001)
Public MeSH Note
2002; see MITOCHONDRIAL MYOPATHIES 2000-2001
History Note
2002; use MITOCHONDRIAL MYOPATHIES 2000-2001
Date Established
2002/01/01
Date of Entry
2001/08/03
Mitochondrial Diseases Preferred
Oxidative Phosphorylation Deficiencies Narrower
Respiratory Chain Deficiencies, Mitochondrial Narrower
Electron Transport Chain Deficiencies, Mitochondrial Narrower
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