DiseaseID 25714
先天性红皮病伴掌跖角化病、少毛症及高免疫球蛋白E
Erythroderma, Congenital, With Palmoplantar Keratoderma, Hypotrichosis, And Hyper-Ige
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Target: 2Links: 2
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 25714
- Core Entity Id
- 118282
- Source Entity Count
- 1
- Preferred Name
- Erythroderma, Congenital, With Palmoplantar Keratoderma, Hypotrichosis, And Hyper-Ige
- Name Cn
- 先天性红皮病伴掌跖角化病、少毛症及高免疫球蛋白E
- Name Pinyin
- Xian Tian Xing Hong Pi Bing Ban Zhang Zhi Jiao Hua Bing 、 Shao Mao Zheng Ji Gao Mian Yi Qiu Dan Bai E
- Name En
- Erythroderma, Congenital, With Palmoplantar Keratoderma, Hypotrichosis, And Hyper-Ige
- 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
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Erythroderma, Congenital, With Palmoplantar Keratoderma, Hypotrichosis, And Hyper-Ige
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Umls
C3809719
Sym Map
SMDE00006
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0