SE-ATLAS

Severe combined immunodeficiency Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency Cernunnos-XLF deficiency Severe combined immunodeficiency due to adenosine deaminase deficiency Immunodeficiency by defective expression of MHC class I Immunodeficiency by defective expression of MHC class II DNA repair defect other than combined T-cell and B-cell immunodeficiencies Immunodeficiency due to selective anti-polysaccharide antibody deficiency Developmental delay-immunodeficiency-leukoencephalopathy-hypohomocysteinemia syndrome Genetic immune deficiency with skin involvement B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome Absent thumb-short stature-immunodeficiency syndrome Facial dysmorphism-immunodeficiency-livedo-short stature syndrome Immunodeficiency due to CD25 deficiency Autoinflammatory syndrome with immune deficiency Good syndrome Immunodeficiency due to MASP-2 deficiency CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome Immunodeficiency due to a complement regulatory deficiency Immunodeficiency due to a complement cascade component deficiency Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity Immunodeficiency due to a classical component pathway complement deficiency Immunodeficiency predominantly affecting antibody production Immune deficiency with skin involvement Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Immunodeficiency with factor I anomaly Non-severe combined immunodeficiency Immunodeficiency with isotype or light chain deficiencies with normal number of B-cells Immunodeficiency with factor H anomaly Acquired immunodeficiency Immunodeficiency due to a complement cascade protein anomaly Immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells FADD-related immunodeficiency Immunodeficiency due to ficolin3 deficiency Immunodeficiency-associated lymphoproliferative disease Familial hyperinflammatory lymphoproliferative immunodeficiency Hoyeraal-Hreidarsson syndrome Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies Hypohidrotic ectodermal dysplasia with immunodeficiency Immunodeficiency due to a late component of complement deficiency Griscelli syndrome