Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
R-numbers: R15 Signed-off version 6.12 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes T-B- SCID, T-B+ SCID, Neutrophil immunodeficiency syndrome 608203, Neutrophil immunodeficiency syndrome, RAS-related C3 Bolutinum toxin substrate 2 deficiency (RAC2), Poor wound healing, leukocytosis, Congenital defects of phagocyte number or function, Reticular dysgenesis, Recurrent sinopulmonary infections, selective IgA defiency, poststreptococcal glomerulonephritis, urticaria |