H01725  Primary immunodeficiency disease
       H02526  Disorders of adaptive immunity
       H00085  Agammaglobulinemias
       H02308  Immunodeficiency-centromeric instability-facial anomalies syndrome
       H00086  Hyper IgM syndromes, autosomal recessive type
       H00088  Common variable immunodeficiency
       H00093  Combined immunodeficiency
       H00091  T-B+Severe combined immunodeficiency
       H00092  T-B-Severe combined immunodeficiency
       H01128  Reticular dysgenesis
       H01244  T+B+Severe combined immunodeficiencies (SCIDs)
       H02309  Adenosine deaminase deficiency
       H02554  Omenn syndrome
       H00984  Bare lymphocyte syndrome type1
       H00985  Bare lymphocyte syndrome type2
       H00087  Other humoral immunodeficiencies
       H00924  Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation
       H01181  T-cell immunodeficiency congenital alopecia and nail dystrophy
       H01387  Activated PI3K-delta syndrome
       H02015  LIG4 syndrome
       H02133  Vici syndrome
       H02585  Roifman-Chitayat syndrome
       H01971  IPEX syndrome
       H00108  Autoimmune lymphoproliferative syndromes
       H01969  X-linked lymphoproliferative syndrome
       H01970  Lymphoproliferative syndrome
       H00109  Familial hemophagocytic lymphohistiocytosis
       H02491  Immunoskeletal dysplasia with neurodevelopmental abnormalities
       H02574  BILU syndrome
       H00064  Ataxia telangiectasia
       H00094  Immunodeficiency associated with DNA repair defects
       H00962  RIDDLE syndrome
       H01344  Nijmegen breakage syndrome
       H01346  Bloom syndrome
       H02014  Ataxia-telangiectasia-like syndrome
       H00580  Schimke immunoosseous dysplasia
       H01264  Hepatic venoocclusive disease with immunodeficiency
       H01968  Hyper-IgE syndrome