DiseaseID 15587

联合氧化磷酸化缺陷4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: 1Target: 3Links: 4
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Record Fields

Scalar fields from the final disease record.

Disease Id
15587
Core Entity Id
73539
Source Entity Count
1
Preferred Name
Combined Oxidative Phosphorylation Deficiency 4
Name Cn
联合氧化磷酸化缺陷4型
Name Pinyin
Lian He Yang Hua Lin Suan Hua Que Xian 4 Xing
Name En
Combined Oxidative Phosphorylation Deficiency 4
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Do Class
genetic disease; disease of metabolism
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
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 4
Role
preferred
Name
COXPD4
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS017457
Omim
610678
Umls
C1857682
Sym Map
SMDE02350
Do Class
DOID:0014667DOID:630
Dis Ge Net
C1857682
Umls Sty
T047
Me Sh Class
C16C18
Tcmbank Disease
29497

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
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
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or Syndrome