SE-ATLAS

Adult idiopathic neutropenia Tumor necrosis factor receptor 1 associated periodic syndrome Complement component 3 deficiency NLRP3-associated autoinflammatory disease Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency Herpes simplex virus encephalitis Hyper-IgE syndrome Kabuki syndrome Hemophagocytic syndrome Good syndrome Immunodeficiency predominantly affecting antibody production Neutrophil immunodeficiency syndrome Activated PI3K-delta syndrome Deafness-lymphedema-leukemia syndrome Severe combined immunodeficiency due to IKK2 deficiency Susceptibility to infection due to TYK2 deficiency Hyper-IgM syndrome type 2 Idiopathic CD4 lymphocytopenia Common variable immunodeficiency Selective IgM deficiency IgG4-related disease Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency X-linked agammaglobulinemia Combined immunodeficiency due to partial RAG1 deficiency Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity Chronic mucocutaneous candidiasis 22q11.2 deletion syndrome Combined immunodeficiency due to CD3gamma deficiency Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency Chronic granulomatous disease Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies Autoimmune lymphoproliferative syndrome Cyclic neutropenia