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Concept information

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Primary Immunodeficiency Diseases > Severe Combined Immunodeficiency
Immune System Diseases > Immunologic Deficiency Syndromes > Primary Immunodeficiency Diseases > Severe Combined Immunodeficiency
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

Terme préférentiel

Severe Combined Immunodeficiency  

Type

  • mesh:Descriptor

Définition

  • 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).

Concept générique

Concepts spécifiques

Synonyme(s)

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

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-PW81FNPK-1

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RDF/XML TURTLE JSON-LD Date de création 03/01/1991, dernière modification le 17/06/2019