Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
R-numbers: R15 Signed-off version 6.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Immunodeficiency, common variable, 3 613493, hypogammaglobulinemia, Immunodeficiency, common variable, 3, Common variable immunodeficiency disorders (CVID), Isolated IgG subclass deficiency, Recurrent infections, may have glomerulonephritis, Predominantly Antibody Deficiencies |