DiseaseID 32596

先天性Horner综合征

Horner Syndrome, Congenital

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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: 19Herb: 12Target: 16Links: 55
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Record Fields

Scalar fields from the final disease record.

Disease Id
32596
Core Entity Id
192530
Source Entity Count
1
Preferred Name
Horner Syndrome, Congenital
Name Cn
先天性Horner综合征
Name Pinyin
Xian Tian Xing Horner Zong He Zheng
Name En
Horner Syndrome, Congenital
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disgenet Type
Mesh Class
Do Class
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
Horner Syndrome, Congenital
Role
preferred
Source
ETCM_v2
Preferred
Yes

Cross References

Trusted external identifiers retained for this final record.

Etcm Disease
Horner Syndrome, Congenital
Itcmdb Generated
ITX-DISEASE-E4FC627F34D5

Attributes

Merged source attributes and domain-specific metadata.

Page Title
Disease Horner Syndrome, Congenital Details page
Basic Information
Disease Name
Horner Syndrome, Congenital
Global Category
Fetal diseases;Rare diseases
Anatomical Category
Eye diseases;Neuronal diseases