Group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an X-linked or autosomal recessive defect. Mutations occurring in many different genes cause human Severe Combined Immunodeficiency (SCID).
SCID — Svår kombinerad immundefekt — Omenns syndrom — Familjär retikuloendotelios
Combined Immunodeficiencies, Severe — Combined Immunodeficiency, Severe — Immunodeficiencies, Severe Combined — Severe Combined Immunodeficiencies — Immunodeficiency Syndrome, Severe Combined — Severe Combined Immunodeficiency Syndrome — Severe Combined Immunologic Deficiency — Immunologic Deficiency, Severe Combined — Severe Combined Immune Deficiency — Immunodeficiency, Severe Combined — Bare Lymphocyte Syndrome — Bare Lymphocyte Syndromes — Lymphocyte Syndrome, Bare — Lymphocyte Syndromes, Bare — Syndrome, Bare Lymphocyte — Syndromes, Bare Lymphocyte — Omenn Syndrome — Syndrome, Omenn — Reticuloendotheliosis, Familial — Familial Reticuloendothelioses — Familial Reticuloendotheliosis — Reticuloendothelioses, Familial — Omenn's Syndrome — Omenns Syndrome — Syndrome, Omenn's