Autosomal dominant combined variable immunodeficiency due to IRF2BP2 mutation

Autosomal dominant combined variable immunodeficiency due to interferon regulatory factor 2 binding protein 2 mutation (disorder)

active

Code	`1354420003`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20241201

Synonyms

Autosomal dominant CVID (combined variable immunodeficiency) due to IRF2BP2 deficiency
Autosomal dominant combined variable immunodeficiency due to IRF2BP2 deficiency
Autosomal dominant combined variable immunodeficiency due to interferon regulatory factor 2 binding protein 2 mutation

Parents (3)

11164009Autosomal dominant hereditary disorder disorder
191010004Common variable immunodeficiency disorder
363138005Hereditary disorder of immune system disorder

Children (0)

None (leaf concept).