DiseaseID 26276
线粒体肌病
Mitochondrial Myopathy
NCI2016_02D:Myopathy caused by mitochondrial abnormalities.|MSH2017_2016_08_12:A group of muscle diseases associated with abnormal mitochondria function.|HPO2016_07_04:A type of myopathy associated with mitochondrial dis
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 3Target: 12Links: 15
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26276
- Core Entity Id
- 118844
- Source Entity Count
- 1
- Preferred Name
- Mitochondrial Myopathy
- Name Cn
- 线粒体肌病
- Name Pinyin
- Xian Li Ti Ji Bing
- Name En
- Mitochondrial Myopathy
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- NCI2016_02D:Myopathy caused by mitochondrial abnormalities.|MSH2017_2016_08_12:A group of muscle diseases associated with abnormal mitochondria function.|HPO2016_07_04:A type of myopathy associated with mitochondrial disease and characterized by findings on biopsy such as ragged red muscle fibers. [HPO:probinson]
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Mitochondrial Myopathy
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Umls
C0162670
Sym Map
SMDE02764
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Disease Definition
NCI2016_02D:Myopathy caused by mitochondrial abnormalities.|MSH2017_2016_08_12:A group of muscle diseases associated with abnormal mitochondria function.|HPO2016_07_04:A type of myopathy associated with mitochondrial disease and characterized by findings on biopsy such as ragged red muscle fibers. [HPO:probinson]