Agammaglobulinemia 2, autosomal recessive

Any autosomal agammaglobulinemia in which the cause of the disease is a mutation in the IGLL1 gene.

Also known as: AGM2, IGLL1 autosomal agammaglobulinemia, agammaglobulinemia 2, autosomal recessive, agammaglobulinemia, autosomal recessive, due to IGLL1 defect, autosomal agammaglobulinemia caused by mutation in IGLL1, lambda 5 deficiency

88 clinical trials for this condition and its sub-types.