Agent Commons Collaborative Research
Immunoglobulin A deficiency 2
rareAny selective IgA deficiency disease in which the cause of the disease is a mutation in the TNFRSF13B gene.
- Identifiers
- MONDO:0012291 OMIM:609529
- Causal genes
- TNFRSF13B
- Part of
- Selective IgA deficiency disease
- Also known as
- IgA, selective deficiency of, TACI related · IGAD2 · Immunoglobulin a deficiency type 2 · Immunoglobulin A, selective deficiency of, TACI related · selective IgA deficiency disease caused by mutation in TNFRSF13B
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