Agammaglobulinemia 2, autosomal recessive

MONDO:0013287

Any autosomal agammaglobulinemia in which the cause of the disease is a mutation in the IGLL1 gene.

Also known as: AGM2, IGLL1 autosomal agammaglobulinemia, agammaglobulinemia 2, autosomal recessive, agammaglobulinemia, autosomal recessive, due to IGLL1 defect, autosomal agammaglobulinemia caused by mutation in IGLL1, lambda 5 deficiency

41 clinical trials for this condition and its sub-types, 0 tagged with Agammaglobulinemia 2, autosomal recessive itself.

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↑ Autosomal agammaglobulinemia (1)

Including sub-types (41) Tagged with Agammaglobulinemia 2, autosomal recessive (0)

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