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immunodeficiency, common variable, 12

Disease Summary
Associated Targets (1)
Tclin

1


Mondo Description Any common variable immunodeficiency in which the cause of the disease is a mutation in the NFKB1 gene.
Uniprot Description A primary immunodeficiency characterized by antibody deficiency, hypogammaglobulinemia, recurrent bacterial infections and an inability to mount an antibody response to antigen.
Mondo Term and Equivalent IDs
MONDO:0014697:  immunodeficiency, common variable, 12
UMLS:C4225277: