DiseaseID 3062

联合氧化磷酸化缺陷32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: 1Formula: 12Target: 18Links: 36
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
3062
Core Entity Id
3464
Source Entity Count
1
Preferred Name
Combined Oxidative Phosphorylation Deficiency 32
Name Cn
联合氧化磷酸化缺陷32型
Name Pinyin
Lian He Yang Hua Lin Suan Hua Que Xian 32 Xing
Name En
Combined Oxidative Phosphorylation Deficiency 32
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
Suppressed

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Combined Oxidative Phosphorylation Deficiency 32
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS030028
Omim
617664
Do Class
DOID:0014667DOID:630
Dis Ge Net
C4540029
Umls Sty
T047
Etcm Disease
Combined Oxidative Phosphorylation Deficiency 32
Itcmdb Generated
ITX-DISEASE-E5AD01EDA010

Attributes

Merged source attributes and domain-specific metadata.

Page Title
Disease Combined Oxidative Phosphorylation Deficiency 32 Details page
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Combined Oxidative Phosphorylation Deficiency 32
Global Category
Genetic diseases;Metabolic diseases
Anatomical Category
Neuronal diseases
Dis Ge Net Disease Type
disease