Summary Literature (0)

DOID:12177 - common variable immunodeficiency

Disease Ontology Definition:An agammaglobulinemia that is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells and that esults in insufficient production of antibodies needed to respond to exposure of pathogens.

Synonyms: CVID, acquired agammaglobulinemia, acquired hypogammaglobulinemia, common variable agammaglobulinemia, sporadic hypogammaglobulinemia,

Echinobase Genes :


OMIM:

MIM:240500 - immunodeficiency, common variable, 2; cvid2

MIM:613493 - immunodeficiency, common variable, 3; cvid3

MIM:613495 - immunodeficiency, common variable, 5; cvid5

MIM:613496 - immunodeficiency, common variable, 6; cvid6

MIM:614700 - immunodeficiency, common variable, 8, with autoimmunity; cvid8

MIM:615577 - immunodeficiency, common variable, 10; cvid10

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee