DiseaseID 11133
线粒体疾病
disease
MSH2017_2016_08_12: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 m
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Disease: 1Symptom: 3Target: 12Links: 15
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 11133
- Core Entity Id
- 68467
- Source Entity Count
- 1
- Preferred Name
- Mitochondrial Diseases
- Name Cn
- 线粒体疾病
- Name Pinyin
- Xian Li Ti Ji Bing
- Name En
- Mitochondrial Diseases
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Nutritional and Metabolic Diseases
- Do Class
- genetic disease; disease of metabolism
- Hpo Class
- Mesh Class Name
- Nutritional and Metabolic Diseases
- Hpo Class Name
- Do Class Name
- disease of metabolism; genetic disease
- Disease Definition
- MSH2017_2016_08_12: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.|CSP2006:diseases caused by abnormal function of the mitochondria; may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components; may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Mitochondrial Diseases
Role
preferred
Name
Electron Transport Chain Deficiencies, Mitochondrial
Role
preferred
Name
Mitochondrial Metabolism Disorder, Unspecified
Role
preferred
Name
Mitochondrial Respiratory Chain Deficiencies
Role
preferred
Name
Oxidative Phosphorylation Deficiencies
Role
preferred
Name
Mitochondrial Metabolism Disease
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS011400HBDIS012568HBDIS012569HBDIS012570HBDIS014277
Me Sh
D028361
Umls
C0751651
Sym Map
SMDE11038
Do Class
DOID:0014667DOID:630
Dis Ge Net
C0751651C0949855C0949856C0949857C1456275
Umls Sty
T047
Me Sh Class
C18
Tcmbank Disease
15881765629361324133928
Itcmdb Generated
ITX-DISEASE-34AD41EA4F2D
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of metabolism; genetic disease
Disease Type
diseasegroup
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Disease Definition
MSH2017_2016_08_12: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.|CSP2006:diseases caused by abnormal function of the mitochondria; may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components; may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.
Me Sh Disease Class
Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
diseasegroup
Disease Class Name Me Sh
Nutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or Syndrome