OBO ID: DOID:12177
Term Name: common variable immunodeficiency Search Ontology:
  • acquired agammaglobulinemia
  • acquired hypogammaglobulinemia
  • common variable agammaglobulinemia
  • CVID
  • sporadic hypogammaglobulinemia
Definition: An agammaglobulinemia that is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells and that esults in insufficient production of antibodies needed to respond to exposure of pathogens. (2)
  • GARD:6140
  • ICD10CM:D83
  • ICD9CM:279.06
  • MESH:D017074
  • OMIM:PS607594
  • ORDO:1572
  • SNOMEDCT_US_2022_03_01:191010004
  • UMLS_CUI:C0009447
Ontology: Human Disease   (DOID:12177)
OTHER common variable immunodeficiency PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available