Agammaglobulinemia 5, autosomal dominant

MONDO:0013290

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

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