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GTR Home > Conditions/Phenotypes > Immunoglobulin A deficiency 2

Summary

Any selective IgA deficiency disease in which the cause of the disease is a mutation in the TNFRSF13B gene. [from MONDO]

Genes See tests for all associated and related genes

  • Also known as: CD267, CVID, CVID2, IGAD2, RYZN, TACI, TNFRSF14B, TNFRSF13B
    Summary: TNF receptor superfamily member 13B

Clinical features

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