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DeCS
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Descriptor English:
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Mitochondrial Diseases
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Descriptor Spanish:
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Enfermedades Mitocondriales
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Descriptor Portuguese:
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Doenças Mitocondriais
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Synonyms English:
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Mitochondrial Disorders
Mitochondrial Electron Transport Chain Deficiencies
Mitochondrial Respiratory Chain Deficiencies
Deficiencies, Oxidative Phosphorylation
Deficiencies, Respiratory Chain
Deficiency, Oxidative Phosphorylation
Deficiency, Respiratory Chain
Disease, Mitochondrial
Disorder, Mitochondrial
Disorders, Mitochondrial
Mitochondrial Disease
Mitochondrial Disorder
Oxidative Phosphorylation Deficiency
Phosphorylation Deficiencies, Oxidative
Phosphorylation Deficiency, Oxidative
Respiratory Chain Deficiency
Electron Transport Chain Deficiencies, Mitochondrial
Oxidative Phosphorylation Deficiencies
Respiratory Chain Deficiencies, Mitochondrial
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Tree Number:
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C18.452.660
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Definition English:
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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. |
Indexing Annotation English:
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GEN or unspecified; prefer specifics
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History Note English:
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2002; use MITOCHONDRIAL MYOPATHIES 2000-2001
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Allowable Qualifiers English:
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Record Number:
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36033
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Unique Identifier:
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D028361
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Occurrence in VHL:
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Similar:
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DeCS CID-10 SciELO LILACS LIS
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