Agammaglobulinemia 8, autosomal dominant

Any autosomal agammaglobulinemia in which the cause of the disease is a mutation in the TCF3 gene.

Also known as: AGM8, TCF3 autosomal agammaglobulinemia, agammaglobulinemia 8, autosomal dominant, agammaglobulinemia 8, autosomal dominant; AGM8, autosomal agammaglobulinemia caused by mutation in TCF3, agammaglobulinemia, autosomal dominant, due to TCF3 defect

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