DiseaseID 18138

联合氧化磷酸化缺陷9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: 1Symptom: 3Target: 1Links: 4
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Record Fields

Scalar fields from the final disease record.

Disease Id
18138
Core Entity Id
76487
Source Entity Count
1
Preferred Name
Combined Oxidative Phosphorylation Deficiency 9
Name Cn
联合氧化磷酸化缺陷9型
Name Pinyin
Lian He Yang Hua Lin Suan Hua Que Xian 9 Xing
Name En
Combined Oxidative Phosphorylation Deficiency 9
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,v2
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Combined Oxidative Phosphorylation Deficiency 9
Role
preferred
Name
COXPD9
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021391
Omim
614582
Umls
C3281234
Sym Map
SMDE01383
Do Class
DOID:0014667DOID:630
Dis Ge Net
C3281234
Umls Sty
T047
Tcmbank Disease
30274

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
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
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome