Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 6Symptom: 4Target: 16Links: 34
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 2618
- Core Entity Id
- 2967
- Source Entity Count
- 1
- Preferred Name
- Combined Oxidative Phosphorylation Deficiency 18
- Name Cn
- 氧化磷酸化联合缺陷症18型 (COXPD18)
- Name Pinyin
- Yang Hua Lin Suan Hua Lian He Que Xian Zheng 18 Xing (coxpd18)
- Name En
- Combined Oxidative Phosphorylation Deficiency 18 (COXPD18)
- 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 18
Role
preferred
Name
COXPD18
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS029504
Omim
615578
Umls
C3810001
Sym Map
SMDE03636
Do Class
DOID:0014667DOID:630
Dis Ge Net
C3810001
Umls Sty
T047
Etcm Disease
Combined Oxidative Phosphorylation Deficiency 18
Itcmdb Generated
ITX-DISEASE-34F6641BD5B1
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Combined Oxidative Phosphorylation Deficiency 18 Details page
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Combined Oxidative Phosphorylation Deficiency 18
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Blood diseases;Eye diseases;Neuronal diseases
Dis Ge Net Disease Type
disease