DiseaseID 26395
科凯恩综合征B型
Cockayne Syndrome B
MSH2017_2016_08_12:Caused by mutations of gene ERCC6.
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Symptom: 12Target: 18Links: 36
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26395
- Core Entity Id
- 118963
- Source Entity Count
- 1
- Preferred Name
- Cockayne Syndrome B
- Name Cn
- 科凯恩综合征B型
- Name Pinyin
- Ke Kai En Zong He Zheng B Xing
- Name En
- Cockayne Syndrome B
- 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
- MSH2017_2016_08_12:Caused by mutations of gene ERCC6.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Cockayne Syndrome B
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C0751038
Sym Map
SMDE03278
Etcm Disease
Cockayne Syndrome B
Itcmdb Generated
ITX-DISEASE-D38A5350F8CB
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Cockayne Syndrome B Details page
Basic Information
Disease Name
Cockayne Syndrome B
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Ear diseases;Eye diseases;Neuronal diseases;Skin diseases
Disease Definition
MSH2017_2016_08_12:Caused by mutations of gene ERCC6.