DiseaseID 26394
Caspase-8缺乏症
Caspase 8 Deficiency
MSH2017_2016_08_12:Autoimmune lymphoproliferative syndrome due to mutations in CASPASE 8 gene.
Relationship Network
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Disease: 1Symptom: 4Target: 20Links: 28
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26394
- Core Entity Id
- 118962
- Source Entity Count
- 1
- Preferred Name
- Caspase 8 Deficiency
- Name Cn
- Caspase-8缺乏症
- Name Pinyin
- Caspase-8 Que Fa Zheng
- Name En
- Caspase 8 Deficiency
- 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:Autoimmune lymphoproliferative syndrome due to mutations in CASPASE 8 gene.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Caspase 8 Deficiency
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C1846545
Sym Map
SMDE03275
Etcm Disease
Caspase 8 Deficiency
Itcmdb Generated
ITX-DISEASE-908FD98E2E28
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Caspase 8 Deficiency Details page
Basic Information
Disease Name
Caspase 8 Deficiency
Global Category
Genetic diseases;Infectious diseases;Rare diseases
Anatomical Category
Blood diseases;Immune diseases
Disease Definition
MSH2017_2016_08_12:Autoimmune lymphoproliferative syndrome due to mutations in CASPASE 8 gene.