Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 7Herb: 6Target: 17Links: 37
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 32399
- Core Entity Id
- 192333
- Source Entity Count
- 1
- Preferred Name
- Fibrinogen Deficiency, Congenital
- Name Cn
- 先天性纤维蛋白原缺乏症
- Name Pinyin
- Xian Tian Xing Xian Wei Dan Bai Yuan Que Fa Zheng
- Name En
- Fibrinogen Deficiency, 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
Fibrinogen Deficiency, Congenital
Role
preferred
Source
ETCM_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Etcm Disease
Fibrinogen Deficiency, Congenital
Itcmdb Generated
ITX-DISEASE-A5644B03A670
Attributes
Merged source attributes and domain-specific metadata.
Page Title
Disease Fibrinogen Deficiency, Congenital Details page
Basic Information
Disease Name
Fibrinogen Deficiency, Congenital
Global Category
Rare diseases
Anatomical Category
Blood diseases