Immunoglobulin A deficiency 2

Any 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

41 clinical trials for this condition and its sub-types, 0 tagged with Immunoglobulin A deficiency 2 itself.