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loading...| Preferred Name | Mitochondrial Encephalomyopathies [Disease/Finding] | |
| Synonyms |
Encephalomyopathies, Mitochondrial Mitochondrial Encephalomyopathies |
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| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000003558 |
|
| altLabel |
Encephalomyopathies, Mitochondrial Mitochondrial Encephalomyopathies |
|
| cui |
C0162666 |
|
| MESH DEFINITION |
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) |
|
| MESH DUI |
D017237 |
|
| MeSH name |
Mitochondrial Encephalomyopathies |
|
| MESH UI |
M0026153 |
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| NDFRT kind |
DISEASE_KIND |
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| notation |
N0000003558 |
|
| NUI |
N0000003558 |
|
| prefLabel |
Mitochondrial Encephalomyopathies [Disease/Finding] |
|
| tui |
T047 |
|
| subClassOf |
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