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Severe Combined Immunodeficiency with Absence of T and B Cells

MedGen UID:
364745
•Concept ID:
C1883020
•
Disease or Syndrome

Definition

An inherited, severe immunodeficiency disorder characterized by abnormalities in the development and function of T and B cell immunity. The peripheral T and B lymphocytes are absent or in very low counts. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVSevere Combined Immunodeficiency with Absence of T and B Cells

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