Panel | Mode of inheritance | Details |
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1 panel | ||
R-numbers: R15 Signed-off version 6.12 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Immunodeficiency due to defect in MAPBP-interacting protein, 610798, Congenital neutropenia, Primary immunodeficiency syndrome due to p14 deficiency, Neutropenia, Hypogammaglobulinemia CD8 cytotoxicity, partial albinism, growth failure, Congenital defects of phagocyte number or function |