DiseaseID 26204
免疫缺陷伴高IgM，3型
Immunodeficiency With Hyper-Igm, Type 3
MSH2017_2016_08_12:Hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 ANTIGEN.
Relationship Network
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Disease: 1Symptom: 1Target: 18Links: 25
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26204
- Core Entity Id
- 118772
- Source Entity Count
- 1
- Preferred Name
- Immunodeficiency With Hyper-Igm, Type 3
- Name Cn
- 免疫缺陷伴高IgM，3型
- Name Pinyin
- Mian Yi Que Xian Ban Gao Igm，3 Xing
- Name En
- Immunodeficiency With Hyper-Igm, Type 3
- 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:Hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 ANTIGEN.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Immunodeficiency With Hyper-Igm, Type 3
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C1720957
Sym Map
SMDE02397
Etcm Disease
Immunodeficiency with Hyper-Igm, Type 3
Itcmdb Generated
ITX-DISEASE-558D1BD15138
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Immunodeficiency with Hyper-Igm, Type 3 Details page
Basic Information
Disease Name
Immunodeficiency with Hyper-Igm, Type 3
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Immune diseases
Disease Definition
MSH2017_2016_08_12:Hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 ANTIGEN.