Common variable immunodeficiency

Common variable immunodeficiency (disorder)

active

Code	`191010004`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20230731

Synonyms

CVID - common variable immunodeficiency
Idiopathic immunoglobulin deficiency
Primary antibody deficiency
Primary hypogammaglobulinaemia
Primary hypogammaglobulinemia

Parents (2)

414030009Disorder of immune structure disorder
58606001Primary immune deficiency disorder disorder

Children (18)

1354420003Autosomal dominant combined variable immunodeficiency due to IRF2BP2 mutation disorder
1354416002Autosomal dominant combined variable immunodeficiency due to NFKB1 mutation disorder
1354480001Autosomal dominant combined variable immunodeficiency due to SEC61A1 mutation disorder
1352026003Autosomal dominant combined variable immunodeficiency due to TWEAK mutation disorder
1354472008Autosomal recessive combined variable immunodeficiency due to ARHGEF1 mutation disorder
1352023006Autosomal recessive combined variable immunodeficiency due to BAFF receptor deficiency disorder
1354483004Autosomal recessive combined variable immunodeficiency due to PIK3CG mutation disorder
1351960005Autosomal recessive common variable immunodeficiency due to CD20 mutation disorder
1351961009Autosomal recessive common variable immunodeficiency due to CD21 mutation disorder
1351267003Autosomal recessive common variable immunodeficiency due to CD81 deficiency disorder
1354596000Autosomal recessive common variable immunodeficiency due to POU2AF1 mutation disorder
1356782005Autosomal recessive common variable immunodeficiency due to RAC2 deficiency disorder
23238000Common variable agammaglobulinaemia disorder
1351268008Common variable immunodeficiency due to TACI deficiency disorder
191013002Common variable immunodeficiency with autoantibodies to B- or T-cells disorder
191011000Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions disorder
191012007Common variable immunodeficiency with predominant immunoregulatory T-cell disorders disorder
1351642008X-linked common variable immunodeficiency due to SH3KBP1 deficiency disorder