Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 5Target: 2Links: 7
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 2400
- Core Entity Id
- 2705
- Source Entity Count
- 1
- Preferred Name
- Combined Oxidative Phosphorylation Deficiency 5
- Name Cn
- 联合氧化磷酸化缺陷症5型
- Name Pinyin
- Lian He Yang Hua Lin Suan Hua Que Xian Zheng 5 Xing
- Name En
- Combined Oxidative Phosphorylation Deficiency 5
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
- 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 5
Role
preferred
Name
COXPD5
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS029107
Omim
611719
Umls
C2673642
Sym Map
SMDE01893
Do Class
DOID:0014667DOID:630
Dis Ge Net
C2673642
Umls Sty
T047
Me Sh Class
C16C18
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease