Immunoglobulin A deficiency 2
MONDO:0012291Any selective IgA deficiency disease in which the cause of the disease is a mutation in the TNFRSF13B gene.
Also known as: Immunoglobulin a deficiency type 2, TNFRSF13B selective IgA deficiency disease, immunoglobulin a deficiency 2, selective IgA deficiency disease caused by mutation in TNFRSF13B, IGAD2, IMMUNOGLOBULIN A deficiency 2, IgA, selective deficiency of, TACI related, IgA, selective deficiency of, TACI-related
88 clinical trials for this condition and its sub-types.
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