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imunodeficiencia kombinovaná ťažká
Č. záznamu d016511 Dátum 06.06.2025 Typ M Tematický termín imunodeficiencia kombinovaná ťažká Iný termín Angličtina (Pseudonym) Bare Lymphocyte Syndrome
Angličtina (Pseudonym) Immunodeficiency, Severe Combined
Angličtina (Pseudonym) Omenn Syndrome
Slovenčina (Pseudonym) Omennov syndróm
Slovenčina (Pseudonym) SCID
Slovenčina (Pseudonym) syndróm nahých lymfocytov
MDT C16.320.798.750C16.614.815C18.452.284.800C20.673.795.750 Poznámka 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). predmetové heslo
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