Concept information
Preferred term
Mitochondrial Diseases
Type
-
Topical Descriptor
Broader concept
Narrower concepts
- 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
Entry terms
- Disorder, Mitochondrial
- Mitochondrial Disorder
- Mitochondrial Disorders
Note
- 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.
History note
- 2002; use MITOCHONDRIAL MYOPATHIES 2000-2001
In other languages
-
Finnish
-
mitokondriosairaudet
-
mitokondriosairaus
-
mitokondriotauti
-
Swedish
-
Mitokondriesjukdomar
-
Oxidativ fosforyleringsbrist
URI
http://www.yso.fi/onto/mesh/D028361
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