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imunodeficiencia kombinovaná ťažká
Record number d016511 Date 06.06.2025 Type M - MESH Topical term imunodeficiencia kombinovaná ťažká Other term English (Pseudonym) Bare Lymphocyte Syndrome
English (Pseudonym) Immunodeficiency, Severe Combined
English (Pseudonym) Omenn Syndrome
Slovak (Pseudonym) Omennov syndróm
Slovak (Pseudonym) SCID
Slovak (Pseudonym) syndróm nahých lymfocytov
UDC C16.320.798.750C16.614.815C18.452.284.800C20.673.795.750 Note 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). 
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