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agammaglobulinemia
Pathology:
- immunodeficiency disorder
- developmental defects in maturation of B-cells
Genetics:
- see Bruton-type agammaglobulinemia
- chromosomal translocation t(9;20)(q33.2;q12) involving LRRC8 is a cause of non-Bruton type agammaglobulinemia
Specific
agammaglobulinemia type 2
Bruton type agammaglobulinemia
X-linked agammaglobulinemia
General
hypogammaglobulinemia; immunoglobulin deficiency
Database Correlations
OMIM 601495