Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
R-numbers: R15 Signed-off version 7.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Immunodeficiency 8, Combined immunodeficiency, hypogammaglobulinaemia, combined immunodeficiency, Coronin-1A deficiency, Atypical Severe Combined Immunodeficiency (Atypical SCID), Severe combined immunodeficiency (SCID), Omenn syndrome, Detectable thymus, EBV, Immunodeficiencies affecting cellular and humoral immunity |