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Medical Subject Headings

Hae sanastosta

Sisällön kieli

Käsitteen tiedot

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Infant, Newborn, Diseases > Severe Combined Immunodeficiency
Nutritional and Metabolic Diseases > Metabolic Diseases > DNA Repair-Deficiency Disorders > Severe Combined Immunodeficiency
Immune System Diseases > Immunologic Deficiency Syndromes > Primary Immunodeficiency Diseases > Severe Combined Immunodeficiency
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Primary Immunodeficiency Diseases > Severe Combined Immunodeficiency

Käytettävä termi

Severe Combined Immunodeficiency  

Tyyppi

  • Topical Descriptor

Yläkäsite

Alakäsitteet

Ohjaustermit

  • Immunodeficiency, Severe Combined
  • Immunodeficiency Syndrome, Severe Combined
  • Immunologic Deficiency, Severe Combined
  • Severe Combined Immune Deficiency
  • Severe Combined Immunodeficiency Syndrome
  • Severe Combined Immunologic Deficiency

Käyttöhuomautus

  • 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).

Huomautus muutoshistoriasta

  • 1992

Muunkieliset termit

URI

http://www.yso.fi/onto/mesh/D016511

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RDF/XML TURTLE JSON-LD Luotu 3.1.1991, viimeksi muokattu 11.4.2022