DiseaseID 18377

联合氧化磷酸化缺陷13型

disease

Back to Browse

Relationship Network

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

Click a node to open it in a new tab
Disease: 1Target: 18Links: 24
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
18377
Core Entity Id
76767
Source Entity Count
1
Preferred Name
Combined Oxidative Phosphorylation Deficiency 13
Name Cn
联合氧化磷酸化缺陷13型
Name Pinyin
Lian He Yang Hua Lin Suan Hua Que Xian 13 Xing
Name En
Combined Oxidative Phosphorylation Deficiency 13
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 13
Role
preferred
Name
COXPD13
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021827
Omim
614932
Umls
C3554129
Sym Map
SMDE03724
Do Class
DOID:0014667DOID:630
Dis Ge Net
C3554129
Umls Sty
T047
Etcm Disease
Combined Oxidative Phosphorylation Deficiency 13
Tcmbank Disease
14371
Itcmdb Generated
ITX-DISEASE-39C34920B682

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Combined Oxidative Phosphorylation Deficiency 13 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 13
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Neuronal diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome