Genetic Basis of Primary Immunodeficiency Disorders (Q167536): Difference between revisions

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description / endescription / en
This cluster of papers focuses on the genetic basis and clinical manifestations of primary immunodeficiency disorders, including immune dysregulation, Th17 cell deficiency, common variable immunodeficiency, and defects in the interferon-? pathway
"Genetic causes of weakened immune systems."

Revision as of 13:47, 30 August 2024

"Genetic causes of weakened immune systems."
  • Primary Immunodeficiency
  • Genetic Mutations
  • Immune Dysregulation
  • Human Inborn Errors
  • Th17 Cell Deficiency
  • Common Variable Immunodeficiency
  • Hematopoietic Stem Cell Transplantation
  • Interferon-? Pathway Defects
  • B Cell Abnormalities
  • Immunoglobulin Replacement Therapy
Language Label Description Also known as
English
Genetic Basis of Primary Immunodeficiency Disorders
"Genetic causes of weakened immune systems."
  • Primary Immunodeficiency
  • Genetic Mutations
  • Immune Dysregulation
  • Human Inborn Errors
  • Th17 Cell Deficiency
  • Common Variable Immunodeficiency
  • Hematopoietic Stem Cell Transplantation
  • Interferon-? Pathway Defects
  • B Cell Abnormalities
  • Immunoglobulin Replacement Therapy

Statements