DiseaseID 18052

联合氧化磷酸化缺陷8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: 1Target: 2Links: 2
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Record Fields

Scalar fields from the final disease record.

Disease Id
18052
Core Entity Id
76382
Source Entity Count
1
Preferred Name
Combined Oxidative Phosphorylation Deficiency 8
Name Cn
联合氧化磷酸化缺陷8型
Name Pinyin
Lian He Yang Hua Lin Suan Hua Que Xian 8 Xing
Name En
Combined Oxidative Phosphorylation Deficiency 8
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 8
Role
preferred
Name
CARDIOMYOPATHY, HYPERTROPHIC MITOCHONDRIAL, FATAL INFANTILE
Role
alias
Name
COXPD8
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021230
Omim
614096
Umls
C3279793
Sym Map
SMDE04251
Do Class
DOID:0014667DOID:630
Dis Ge Net
C3279793
Umls Sty
T047
Etcm Disease
Combined Oxidative Phosphorylation Deficiency 8
Tcmbank Disease
10722
Itcmdb Generated
ITX-DISEASE-C0153CEFBDE1

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Combined Oxidative Phosphorylation Deficiency 8 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 8
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome