DiseaseID 19315

联合氧化磷酸化缺陷24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: 6Target: 20Links: 30
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Record Fields

Scalar fields from the final disease record.

Disease Id
19315
Core Entity Id
77822
Source Entity Count
1
Preferred Name
Combined Oxidative Phosphorylation Deficiency 24
Name Cn
联合氧化磷酸化缺陷24型
Name Pinyin
Lian He Yang Hua Lin Suan Hua Que Xian 24 Xing
Name En
Combined Oxidative Phosphorylation Deficiency 24
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 24
Role
preferred
Name
COXPD24
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS023139
Omim
616239
Umls
C4015643
Sym Map
SMDE04373
Do Class
DOID:0014667DOID:630
Dis Ge Net
C4015643
Umls Sty
T047
Etcm Disease
Combined Oxidative Phosphorylation Deficiency 24
Tcmbank Disease
28876
Itcmdb Generated
ITX-DISEASE-E274437A9314

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Combined Oxidative Phosphorylation Deficiency 24 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 24
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