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GTR Home > Conditions/Phenotypes > Agammaglobulinemia 3, autosomal recessive

Summary

Any autosomal agammaglobulinemia in which the cause of the disease is a mutation in the CD79A gene. [from MONDO]

Genes See tests for all associated and related genes

  • Also known as: IGA, IGAlpha, MB-1, MB1, CD79A
    Summary: CD79a molecule

Clinical features

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