SE-ATLAS

Severe combined immunodeficiency Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency Cernunnos-XLF deficiency Immunodeficiency by defective expression of MHC class II Severe combined immunodeficiency due to adenosine deaminase deficiency Immunodeficiency by defective expression of MHC class I Absent thumb-short stature-immunodeficiency syndrome Immunodeficiency due to CD25 deficiency Immunodeficiency due to selective anti-polysaccharide antibody deficiency Developmental delay-immunodeficiency-leukoencephalopathy-hypohomocysteinemia syndrome Genetic immune deficiency with skin involvement Facial dysmorphism-immunodeficiency-livedo-short stature syndrome CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome Good syndrome Immunodeficiency due to MASP-2 deficiency Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity Immunodeficiency due to a complement regulatory deficiency Immunodeficiency due to a complement cascade component deficiency Immunodeficiency due to a classical component pathway complement deficiency T-B+ severe combined immunodeficiency due to JAK3 deficiency Autoinflammatory syndrome with immune deficiency Severe combined immunodeficiency due to DCLRE1C deficiency T-B+ severe combined immunodeficiency due to gamma chain deficiency Combined immunodeficiency-enteropathy spectrum Immune deficiency with skin involvement Combined immunodeficiency due to RELA haploinsufficiency Non-severe combined immunodeficiency Common variable immunodeficiency Pancytopenia due to IKZF1 mutations Acquired immunodeficiency Combined immunodeficiency due to OX40 deficiency Combined immunodeficiency due to DOCK8 deficiency Primary immunodeficiency with predisposition to severe viral infection Laron syndrome with immunodeficiency Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection Primary immunodeficiency due to a defect in adaptive immunity PLCG2-associated antibody deficiency and immune dysregulation Combined immunodeficiency due to STK4 deficiency Combined immunodeficiency due to CD70 deficiency Severe combined immunodeficiency due to LCK deficiency Combined immunodeficiency due to CARMIL2 deficiency Immunodeficiency predominantly affecting antibody production Combined immunodeficiency due to ITK deficiency Combined immunodeficiency due to LRBA deficiency Primary immunodeficiency due to a defect in innate immunity Immunodeficiency due to a complement cascade protein anomaly Combined immunodeficiency due to CARD11 deficiency FADD-related immunodeficiency Combined immunodeficiency due to FCHO1 deficiency Combined immunodeficiency due to CD3gamma deficiency Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome Griscelli syndrome Primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency DNA repair defect other than combined T-cell and B-cell immunodeficiencies Combined immunodeficiency due to CRAC channel dysfunction Omenn syndrome Severe combined immunodeficiency due to FOXN1 deficiency Nijmegen breakage syndrome Immunodeficiency syndrome with autoimmunity Combined immunodeficiency due to MALT1 deficiency Combined immunodeficiency due to GINS1 deficiency Combined immunodeficiency due to ZAP70 deficiency Autosomal recessive combined immunodeficiency due to complete IL6ST deficiency Immune dysregulation disease with immunodeficiency Neutrophil immunodeficiency syndrome Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome Severe combined immunodeficiency due to CORO1A deficiency PGM3-CDG Autosomal recessive combined immunodeficiency due to partial IL6ST deficiency Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency Combined immunodeficiency due to CD27 deficiency Immune deficiency due to impaired neutrophil phagocytosis and migration Immunodeficiency due to ficolin3 deficiency Autosomal dominant combined immunodeficiency due to partial IL6ST deficiency Familial hyperinflammatory lymphoproliferative immunodeficiency Immunodeficiency due to a late component of complement deficiency X-linked combined immunodeficiency due to SASH3 deficiency T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome Severe combined immunodeficiency due to complete RAG1/2 deficiency B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome T-B+ severe combined immunodeficiency due to CD45 deficiency T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta Autosomal recessive combined immunodeficiency due to IL6R deficiency Severe combined immunodeficiency due to CTPS1 deficiency Severe combined immunodeficiency due to IKK2 deficiency Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Immunodeficiency with factor I anomaly Periodic fever-immunodeficiency-thrombocytopenia syndrome Immunodeficiency with isotype or light chain deficiencies with normal number of B-cells Immunodeficiency with factor H anomaly T-B+ severe combined immunodeficiency Immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells T-B- severe combined immunodeficiency Combined immunodeficiency due to ORAI1 deficiency Combined immunodeficiency due to partial RAG1 deficiency Combined immunodeficiency due to STIM1 deficiency Immunodeficiency-associated lymphoproliferative disease Severe combined immunodeficiency due to DNA-PKcs deficiency NIK deficiency Hoyeraal-Hreidarsson syndrome Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies Hypohidrotic ectodermal dysplasia with immunodeficiency Combined immunodeficiency with granulomatosis Combined immunodeficiency due to DOCK2 deficiency T-cell immunodeficiency with thymic aplasia Autosomal dominant combined immunodeficiency due to ERBIN deficiency X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome Say-Barber-Miller syndrome Reticular dysgenesis Combined T and B cell immunodeficiency Deficiency in anterior pituitary function-variable immunodeficiency syndrome Primary immunodeficiency Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome Methylenetetrahydrofolate dehydrogenase 1 deficiency Spondylometaphyseal dysplasia with combined immunodeficiency RIDDLE syndrome Wiskott-Aldrich syndrome Early-onset autoimmunity-autoinflammation-immunodeficiency syndrome Primary immunodeficiency syndrome due to LAMTOR2 deficiency Short-limb skeletal dysplasia with severe combined immunodeficiency Other immunodeficiency syndromes due to defects in innate immunity T-cell immunodeficiency with epidermodysplasia verruciformis Severe combined immunodeficiency due to LAT deficiency Immunodeficiency due to absence of thymus Syndrome with combined immunodeficiency Combined immunodeficiency due to Moesin deficiency Combined immunodeficiency due to TFRC deficiency LIG4 syndrome Other immunodeficiency syndrome with predominantly antibody defects T+ B+ severe combined immunodeficiency Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome