Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 12Symptom: 4Target: 20Links: 40
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 2559
- Core Entity Id
- 2896
- Source Entity Count
- 1
- Preferred Name
- Combined Oxidative Phosphorylation Deficiency 10
- Name Cn
- 联合氧化磷酸化缺陷10型
- Name Pinyin
- Lian He Yang Hua Lin Suan Hua Que Xian 10 Xing
- Name En
- Combined Oxidative Phosphorylation Deficiency 10
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Do Class
- genetic disease; disease of metabolism
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Combined Oxidative Phosphorylation Deficiency 10
Role
preferred
Name
CARDIOMYOPATHY, INFANTILE HYPERTROPHIC MITOCHONDRIAL, AND LACTIC ACIDOSIS
Role
alias
Name
COXPD10
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS029398
Omim
614702
Umls
C3553529
Sym Map
SMDE02890
Do Class
DOID:0014667DOID:630
Dis Ge Net
C3553529
Umls Sty
T047
Etcm Disease
Combined Oxidative Phosphorylation Deficiency 10
Itcmdb Generated
ITX-DISEASE-447EB5D38AAF
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Combined Oxidative Phosphorylation Deficiency 10 Details page
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Combined Oxidative Phosphorylation Deficiency 10
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Cardiovascular diseases
Dis Ge Net Disease Type
disease