Combined immunodeficiencies
Notes: ADA deficiency NOS ; ADA deficiency with SCID ; Adenosine deaminase [ADA] deficiency with severe combined immunodeficiency ; ADA2 deficiency ; Adenosine deaminase deficiency type 2 ; Adenosine deaminase [ADA] deficiency type 1, NOS ; Adenosine deaminase [ADA] deficiency type 1, without SCID ; Adenosine deaminase [ADA] deficiency type 1, without severe combined immunodeficiency ; Partial ADA deficiency (type 1) ; Partial adenosine deaminase deficiency (type 1) ; Bare lymphocyte syndrome ; Multiple carboxylase deficiency ; Holocarboxylase synthetase deficiency ; Other multiple carboxylase deficiency ; Multiple carboxylase deficiency, unspecified ; p110d-activating mutation causing senescent T cells, lymphadenopathy, and immunodeficiency [PASLI] disease ; Severe combined immunodeficiency disorder [SCID] NOS ; autosomal recessive agammaglobulinemia (Swiss type) (D80.0) ; biotin-dependent carboxylase deficiency due to dietary deficiency of biotin (E53.8)