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

41 clinical trials for this condition and its sub-types, 0 tagged with Agammaglobulinemia 8, autosomal dominant itself.

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↑ Autosomal agammaglobulinemia (1)

Including sub-types (41) Tagged with Agammaglobulinemia 8, autosomal dominant (0)

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