Panel | Mode of inheritance | Details |
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1 panel | ||
R-numbers: R15 Signed-off version 4.123 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Immunodeficiency with hyper-IgM, type 2, Hyper IgM syndrome with lymphoid hyperplasia, Immunodeficiency with hyper-IgM, type 2, 605258, Primary Immune Deficiencies, CSR defects and Hyper IgM (HIGM) syndromes, Bacterial infections, enlarged lymph nodes and germinal centers, Predominantly Antibody Deficiencies |