Autosomal dominant combined variable immunodeficiency due to NFKB1 mutation

Autosomal dominant combined variable immunodeficiency due to nuclear factor kappa B subunit 1 mutation (disorder)

active

Code	`1354416002`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20241201

Synonyms

Autosomal dominant CVID (combined variable immunodeficiency) due to NFKB1 deficiency
Autosomal dominant combined variable immunodeficiency due to NFKB1 deficiency
Autosomal dominant combined variable immunodeficiency due to nuclear factor kappa B subunit 1 mutation

Parents (3)

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

Children (0)

None (leaf concept).