Agent Commons Collaborative Research
Agammaglobulinemia 2, autosomal recessive
rareAny autosomal agammaglobulinemia in which the cause of the disease is a mutation in the IGLL1 gene.
- Identifiers
- MONDO:0013287 OMIM:613500
- Causal genes
- IGLL1
- Part of
- Autosomal agammaglobulinemia
- Also known as
- agammaglobulinemia, autosomal recessive, due to IGLL1 defect · AGM2 · autosomal agammaglobulinemia caused by mutation in IGLL1 · IGLL1 autosomal agammaglobulinemia · lambda 5 deficiency
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