Agammaglobulinemia 3, autosomal recessive

Any autosomal agammaglobulinemia in which the cause of the disease is a mutation in the CD79A gene.

Also known as: CD79A autosomal agammaglobulinemia, agammaglobulinemia 3, autosomal recessive, autosomal agammaglobulinemia caused by mutation in CD79A, AGM3, agammaglobulinemia, autosomal recessive, due to Cd79A defect

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