Common Variable Immunodeficiency (CVID)

Alias:
Cvid
Idiopathic Immunoglobulin Deficiency
Acquired Hypogammaglobulinemia
Primary Hypogammaglobulinemia
Primary Antibody Deficiency
Common Variable Hypogammaglobulinemia
Common Variable Agammaglobulinemia
Common Variable Immune Deficiency
Immunodeficiency, Common Variable
Sporadic Hypogammaglobulinemia
Acquired Agammaglobulinemia
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Common Variable Immunodeficiency, also known as cvid, is related to immunodeficiency, common variable, 1 and immunodeficiency, common variable, 2. An important gene associated with Common Variable Immunodeficiency is TNFRSF13B (TNF Receptor Superfamily Member 13B), and among its related pathways/superpathways are ERK Signaling and Innate Immune System. The drugs Rifaximin and Budesonide have been mentioned in the context of this disorder. Affiliated tissues include t cells and b cells, and related phenotypes are chronic otitis media and recurrent respiratory infections
Related ID:
MESH:D017074

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
AD
All ages
<1/1000000
111
1401
38

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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