Agammaglobulinemia 4, autosomal recessive

MONDO:0013289

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

Also known as: AGM4, B cell linker protein deficiency, BLNK autosomal agammaglobulinemia, agammaglobulinemia 4, autosomal recessive, agammaglobulinemia, autosomal recessive, due to Blnk defect, autosomal agammaglobulinemia caused by mutation in BLNK

41 clinical trials for this condition and its sub-types, 0 tagged with Agammaglobulinemia 4, autosomal recessive itself.

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↑ Autosomal agammaglobulinemia (1)

Including sub-types (41) Tagged with Agammaglobulinemia 4, autosomal recessive (0)

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