Agammaglobulinemia 8, autosomal dominant

MONDO:0014840

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

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