DiseaseID 18378

联合氧化磷酸化缺陷14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: 7Target: 1Links: 8
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Record Fields

Scalar fields from the final disease record.

Disease Id
18378
Core Entity Id
76768
Source Entity Count
1
Preferred Name
Combined Oxidative Phosphorylation Deficiency 14
Name Cn
联合氧化磷酸化缺陷14型
Name Pinyin
Lian He Yang Hua Lin Suan Hua Que Xian 14 Xing
Name En
Combined Oxidative Phosphorylation Deficiency 14
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 14
Role
preferred
Name
COXPD14
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021829
Omim
614946
Umls
C3554168
Sym Map
SMDE01495
Do Class
DOID:0014667DOID:630
Dis Ge Net
C3554168
Umls Sty
T047
Tcmbank Disease
27378

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