DiseaseID 2675

联合氧化磷酸化缺陷症23型

disease

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Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

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Disease: 1Formula: 20Herb: 8Symptom: 5Target: 17Links: 57
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Record Fields

Scalar fields from the final disease record.

Disease Id
2675
Core Entity Id
3034
Source Entity Count
1
Preferred Name
Combined Oxidative Phosphorylation Deficiency 23
Name Cn
联合氧化磷酸化缺陷症23型
Name Pinyin
Lian He Yang Hua Lin Suan Hua Que Xian Zheng 23 Xing
Name En
Combined Oxidative Phosphorylation Deficiency 23
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 23
Role
preferred
Name
COXPD23
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS029594
Omim
616198
Umls
C4015447
Sym Map
SMDE00058
Do Class
DOID:0014667DOID:630
Dis Ge Net
C4015447
Umls Sty
T047
Etcm Disease
Combined Oxidative Phosphorylation Deficiency 23
Itcmdb Generated
ITX-DISEASE-504A1A2EFD14

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Combined Oxidative Phosphorylation Deficiency 23 Details page
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Combined Oxidative Phosphorylation Deficiency 23
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Cardiovascular diseases;Neuronal diseases
Dis Ge Net Disease Type
disease