SE-ATLAS

Severe combined immunodeficiency due to DNA-PKcs deficiency Severe combined immunodeficiency Severe combined immunodeficiency due to CORO1A deficiency Combined immunodeficiency due to CRAC channel dysfunction Combined immunodeficiency due to LRBA deficiency Hereditary angioedema Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection C1 inhibitor deficiency Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency Hereditary angioedema type 1 Severe combined immunodeficiency due to DCLRE1C deficiency Immunoglobulin heavy chain deficiency Transient hypogammaglobulinemia of infancy X-linked agammaglobulinemia Hyper-IgM syndrome with susceptibility to opportunistic infections Cernunnos-XLF deficiency Hyper-IgM syndrome type 4 Leukocyte adhesion deficiency type II T-B+ severe combined immunodeficiency due to JAK3 deficiency T-cell immunodeficiency with thymic aplasia T-B+ severe combined immunodeficiency due to gamma chain deficiency Severe combined immunodeficiency due to adenosine deaminase deficiency Immunodeficiency by defective expression of MHC class I Common variable immunodeficiency 22q11.2 deletion syndrome Immunodeficiency by defective expression of MHC class II Autosomal agammaglobulinemia Combined immunodeficiency due to CARD11 deficiency Omenn syndrome Wiskott-Aldrich syndrome X-linked lymphoproliferative disease Combined immunodeficiency due to ZAP70 deficiency WHIM syndrome Hyper-IgE syndrome Hereditary angioedema type 2 Severe combined immunodeficiency due to IKK2 deficiency LIG4 syndrome T-B+ severe combined immunodeficiency T-B- severe combined immunodeficiency Purine nucleoside phosphorylase deficiency Agammaglobulinemia