DiseaseID 2663

联合氧化磷酸化缺陷症22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: 2Target: 1Links: 3
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
2663
Core Entity Id
3020
Source Entity Count
1
Preferred Name
Combined Oxidative Phosphorylation Deficiency 22
Name Cn
联合氧化磷酸化缺陷症22型
Name Pinyin
Lian He Yang Hua Lin Suan Hua Que Xian Zheng 22 Xing
Name En
Combined Oxidative Phosphorylation Deficiency 22
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 22
Role
preferred
Name
COXPD22
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS029579
Omim
616045
Umls
C4015062
Sym Map
SMDE00126
Do Class
DOID:0014667DOID:630
Dis Ge Net
C4015062
Umls Sty
T047

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
Dis Ge Net Disease Type
disease