Begreppsinformation
Föredragen term
Mitochondrial Diseases
Typ
-
Topical Descriptor
Överordnat begrepp
Underordnade begrepp
- 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
Hänvisningstermer
- Disorder, Mitochondrial
- Disorders, Mitochondrial
- Mitochondrial Disorder
- Mitochondrial Disorders
Anmärkning
- general or unspecified; prefer specifics
Användningsanmärkning
- 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.
Anmärkning om ändringshistoria
- 2002; use MITOCHONDRIAL MYOPATHIES 2000-2001
Termer på andra språk
-
finska
-
mitokondriosairaudet
-
mitokondriosairaus
-
mitokondriotauti
-
svenska
URI
http://www.yso.fi/onto/mesh/D028361
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