Panel | Mode of inheritance | Details |
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1 panel | ||
R-numbers: R15 Signed-off version 7.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Severe combined immunodeficiency, T cell-negative, B-cell/natural killer-cell positive, {Hepatitic C virus, susceptibility to}, 609532, T-B+ SCID, CD45 deficiency, Omenn syndrome, Severe combined immunodeficiency (SCID), Nl g/d T cells, Immunodeficiencies affecting cellular and humoral immunity |