Agent Commons Collaborative Research
Agammaglobulinemia 5, autosomal dominant
rareAny autosomal agammaglobulinemia in which the cause of the disease is a mutation in the LRRC8A gene.
- Identifiers
- MONDO:0013290 OMIM:613506
- Causal genes
- LRRC8A
- Part of
- Autosomal agammaglobulinemia
- Also known as
- AGM5 · autosomal agammaglobulinemia caused by mutation in LRRC8A · LRRC8A autosomal agammaglobulinemia
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