DiseaseID 26420
科凯恩综合征A型
Cockayne Syndrome A
MSH2017_2016_08_12:Caused by mutations of gene CKN1.
Relationship Network
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Disease: 1Symptom: 12Target: 20Links: 36
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26420
- Core Entity Id
- 118988
- Source Entity Count
- 1
- Preferred Name
- Cockayne Syndrome A
- Name Cn
- 科凯恩综合征A型
- Name Pinyin
- Ke Kai En Zong He Zheng A Xing
- Name En
- Cockayne Syndrome A
- 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 CKN1.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Cockayne Syndrome A
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C0751039
Sym Map
SMDE03379
Etcm Disease
Cockayne Syndrome a
Itcmdb Generated
ITX-DISEASE-D405E42E9F74
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Cockayne Syndrome a Details page
Basic Information
Disease Name
Cockayne Syndrome a
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 CKN1.