| Descriptor English: | Mitochondrial Diseases | ||||||
| Descriptor Spanish: |
Enfermedades Mitocondriales
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| Descriptor Portuguese: | Doenças Mitocondriais | ||||||
| Descriptor French: | Maladies mitochondriales | ||||||
| Entry term(s): |
Deficiencies, Oxidative Phosphorylation Deficiencies, Respiratory Chain Deficiency, Oxidative Phosphorylation Deficiency, Respiratory Chain Disease, Mitochondrial Disorder, Mitochondrial Disorders, Mitochondrial Electron Transport Chain Deficiencies, Mitochondrial Mitochondrial Disease Mitochondrial Disorder Mitochondrial Disorders Mitochondrial Electron Transport Chain Deficiencies Mitochondrial Respiratory Chain Deficiencies Oxidative Phosphorylation Deficiencies Oxidative Phosphorylation Deficiency Phosphorylation Deficiencies, Oxidative Phosphorylation Deficiency, Oxidative Respiratory Chain Deficiencies, Mitochondrial Respiratory Chain Deficiency |
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| Tree number(s): |
C18.452.660 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D028361 | ||||||
| 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. |
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| Annotation: | general or unspecified; prefer specifics |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Mitochondria (1987-2001) Mitochondrial Myopathies (1992-2001) |
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| Public MeSH Note: | 2002; see MITOCHONDRIAL MYOPATHIES 2000-2001 |
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| History Note: | 2002; use MITOCHONDRIAL MYOPATHIES 2000-2001 |
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| Entry Version: | MITOCHONDRIAL DIS |
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| DeCS ID: | 36033 | ||||||
| Unique ID: | D028361 | ||||||
| NLM Classification: | WD 200.5.M6 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2002/01/01 | ||||||
| Date of Entry: | 2001/08/03 |
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Mitochondrial Diseases
- Preferred
Oxidative Phosphorylation Deficiencies
- Narrower
Respiratory Chain Deficiencies, Mitochondrial
- Narrower
Electron Transport Chain Deficiencies, Mitochondrial
- Narrower
| Concept UI |
M0335637 |
| 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. |
| Preferred term | Mitochondrial Diseases |
| Entry term(s) |
Disease, Mitochondrial Disorder, Mitochondrial Disorders, Mitochondrial Mitochondrial Disease Mitochondrial Disorder Mitochondrial Disorders |
| Concept UI |
M0382031 |
| Preferred term | Oxidative Phosphorylation Deficiencies |
| Entry term(s) |
Deficiencies, Oxidative Phosphorylation Deficiency, Oxidative Phosphorylation Oxidative Phosphorylation Deficiency Phosphorylation Deficiencies, Oxidative Phosphorylation Deficiency, Oxidative |
| Concept UI |
M0382030 |
| Preferred term | Respiratory Chain Deficiencies, Mitochondrial |
| Entry term(s) |
Deficiencies, Respiratory Chain Deficiency, Respiratory Chain Mitochondrial Respiratory Chain Deficiencies Respiratory Chain Deficiency |
| Concept UI |
M0387124 |
| Preferred term | Electron Transport Chain Deficiencies, Mitochondrial |
| Entry term(s) |
Mitochondrial Electron Transport Chain Deficiencies |
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