NFKB2

nuclear factor kappa B subunit 2
OMIM: 164012
PanelMode of inheritanceDetails
3 panels
R-numbers: R163
Signed-off version 1.10
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Immunodeficiency, common variable, 10 615577
R-numbers: R15
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Immunodeficiency, common variable, 10 615577, Hypogammaglobuliaemia, immune dysregulation, central adrenal insufficiency, Common variable immunodeficiency disorders (CVID), Unclassified antibody deficiency, Recurrent sinopulmonary infections, alopecia and endorinopathies, Predominantly Antibody Deficiencies
R-numbers: R189
Signed-off version 1.3
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Immunodeficiency, common variable, 10, 615577, Bronchiectasis