DiseaseID 26294
X连锁联合免疫缺陷
Combined Immunodeficiency, X-Linked
NCI2016_02D:Rare congenital disorder inherited as an X-linked defect characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels.|MSH2017_2016_08_12:Forms of comb
Relationship Network
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Disease: 1Herb: 5Symptom: 2Target: 16Links: 31
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26294
- Core Entity Id
- 118862
- Source Entity Count
- 1
- Preferred Name
- Combined Immunodeficiency, X-Linked
- Name Cn
- X连锁联合免疫缺陷
- Name Pinyin
- X Lian Suo Lian He Mian Yi Que Xian
- Name En
- Combined Immunodeficiency, X-Linked
- 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
- NCI2016_02D:Rare congenital disorder inherited as an X-linked defect characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels.|MSH2017_2016_08_12:Forms of combined immunodeficiency caused by mutations in the gene for INTERLEUKIN RECEPTOR COMMON GAMMA SUBUNIT. Both severe and non-severe subtypes of the disease have been identified.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Combined Immunodeficiency, X-Linked
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C1279481
Sym Map
SMDE02856
Etcm Disease
Combined Immunodeficiency, X-Linked
Itcmdb Generated
ITX-DISEASE-84F8E192F3BE
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Combined Immunodeficiency, X-Linked Details page
Basic Information
Disease Name
Combined Immunodeficiency, X-Linked
Global Category
Genetic diseases
Anatomical Category
Immune diseases
Disease Definition
NCI2016_02D:Rare congenital disorder inherited as an X-linked defect characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels.|MSH2017_2016_08_12:Forms of combined immunodeficiency caused by mutations in the gene for INTERLEUKIN RECEPTOR COMMON GAMMA SUBUNIT. Both severe and non-severe subtypes of the disease have been identified.