Agammaglobulinemia 5, autosomal dominant

Any autosomal agammaglobulinemia in which the cause of the disease is a mutation in the LRRC8A gene.

Also known as: LRRC8A autosomal agammaglobulinemia, agammaglobulinemia 5, autosomal dominant, autosomal agammaglobulinemia caused by mutation in LRRC8A, AGM5, agammaglobulinemia, autosomal dominant, due to Lrrc8A defect

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