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Summary Literature (0)
DOID:0081154 - common variable immunodeficiency 12

Disease Ontology Definition:A common variable immunodeficiency that is characterized by recurrent infections and associated with hypogammaglobulinemia and that has_material_basis_in heterozygous mutation in the NFKB1 gene on chromosome 4q24.

Synonyms:

Xenbase Genes : nfkb1



Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): common variable immunodeficiency (is_a)