DiseaseID 26331
伴IgM增高的免疫缺陷1型
Immunodeficiency With Hyper-Igm, Type 1
MSH2017_2016_08_12:An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND.
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: 1Herb: 1Symptom: 9Target: 17Links: 34
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26331
- Core Entity Id
- 118899
- Source Entity Count
- 1
- Preferred Name
- Immunodeficiency With Hyper-Igm, Type 1
- Name Cn
- 伴IgM增高的免疫缺陷1型
- Name Pinyin
- Ban Igm Zeng Gao De Mian Yi Que Xian 1 Xing
- Name En
- Immunodeficiency With Hyper-Igm, Type 1
- 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:An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Immunodeficiency With Hyper-Igm, Type 1
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C0398689
Sym Map
SMDE02997
Etcm Disease
Immunodeficiency with Hyper-Igm, Type 1
Itcmdb Generated
ITX-DISEASE-1106CE49D3F3
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Immunodeficiency with Hyper-Igm, Type 1 Details page
Basic Information
Disease Name
Immunodeficiency with Hyper-Igm, Type 1
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Immune diseases
Disease Definition
MSH2017_2016_08_12:An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND.