| Descriptor English: | Mitochondrial Encephalomyopathies | ||||
| Descriptor Spanish: |
Encefalomiopatías Mitocondriales
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| Descriptor Portuguese: | Encefalomiopatias Mitocondriais | ||||
| Descriptor French: | Encéphalomyopathies mitochondriales | ||||
| Entry term(s): |
Encephalomyopathies, Mitochondrial Encephalomyopathy, Mitochondrial Mitochondrial Encephalomyopathy |
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| Tree number(s): |
C05.651.460.620 C10.228.140.163.540 C10.668.491.500.500 C18.452.132.540 C18.452.660.560.620 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D017237 | ||||
| Scope note: | A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5) |
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| Annotation: | general or unspecified; prefer specifics; coordinate with specific dysfunction if pertinent |
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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: |
Brain Diseases, Metabolic (1977-1992) Mitochondria, Muscle (1977-1992) Neuromuscular Diseases (1977-1992) |
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| Public MeSH Note: | 1993 |
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| History Note: | 1993 |
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| Entry Version: | MITOCHONDRIAL ENCEPH |
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| DeCS ID: | 30655 | ||||
| Unique ID: | D017237 | ||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
| Date Established: | 1993/01/01 | ||||
| Date of Entry: | 1992/05/22 | ||||
| Revision Date: | 2006/07/05 |
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Mitochondrial Encephalomyopathies
- Preferred
| Concept UI |
M0026153 |
| Scope note | A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5) |
| Preferred term | Mitochondrial Encephalomyopathies |
| Entry term(s) |
Encephalomyopathies, Mitochondrial Encephalomyopathy, Mitochondrial Mitochondrial Encephalomyopathy |
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