Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 1Target: 16Links: 25
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 18724
- Core Entity Id
- 77167
- Source Entity Count
- 1
- Preferred Name
- Combined Oxidative Phosphorylation Deficiency 17
- Name Cn
- 联合氧化磷酸化缺陷17型
- Name Pinyin
- Lian He Yang Hua Lin Suan Hua Que Xian 17 Xing
- Name En
- Combined Oxidative Phosphorylation Deficiency 17
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- 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 of metabolism; genetic disease
- Disease Definition
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Combined Oxidative Phosphorylation Deficiency 17
Role
preferred
Name
COXPD17
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS022356
Omim
615440
Umls
C3809526
Sym Map
SMDE00417
Do Class
DOID:0014667DOID:630
Dis Ge Net
C3809526
Umls Sty
T047
Etcm Disease
Combined Oxidative Phosphorylation Deficiency 17
Tcmbank Disease
31594
Itcmdb Generated
ITX-DISEASE-094A367A2772
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Combined Oxidative Phosphorylation Deficiency 17 Details page
Do Class Name
disease of metabolism; genetic disease
Disease Type
disease
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Combined Oxidative Phosphorylation Deficiency 17
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Cardiovascular diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome