Specific

agammaglobulinemia type 2 antiphospholipid syndrome (APS); Hughes syndrome autoimmune lymphoproliferative syndrome (ALPS, Canale-Smith syndrome) autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED); autoimmune polyglandular syndrome type 1; Whitaker's syndrome Chediak-Higashi syndrome combined immune deficiency; severe combined immunodeficiency disease (SCID CID) complement C2 deficiency eosinophil peroxidase deficiency familial candidiasis familial histiocytic reticulosis; familial hemophagocytic reticulosis; familial hemophagocytic lymphohistiocytosis; familial erythrophagocytic lymphohistiocytosis ficolin-3 deficiency Griscelli syndrome hereditary periodic fever syndrome; periodic fevers; recurrent fever syndrome; familial autoinflammatory disease hyper IgE recurrent infection syndrome autosomal recessive hypoglobulinemia & absent B-cells IRAK4 deficiency LFA-1 immunodeficiency disease Mendelian susceptibility to mycobacterial disease (MSMD); familial disseminated atypical mycobacterial infection recurrent invasive pneumococcal disease STAT1 deficiency

General

chronic immunologic disease genetic disease