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imunodeficiencia kombinovaná ťažká

  1. Subject h.imunodeficiencia kombinovaná ťažká
    Subject h.Severe Combined Immunodeficiency
    Entry termsOmennov syndróm
    SCID
    syndróm nahých lymfocytov
    English X referencesBare Lymphocyte Syndrome
    Immunodeficiency, Severe Combined
    Omenn Syndrome
    Scope note in EnglishGroup 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).
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