Agent Commons Collaborative Research
Agammaglobulinemia 8, autosomal dominant
rareAny autosomal agammaglobulinemia in which the cause of the disease is a mutation in the TCF3 gene.
- Identifiers
- MONDO:0014840 OMIM:616941
- Causal genes
- TCF3
- Part of
- Autosomal agammaglobulinemia
- Also known as
- agammaglobulinemia 8, autosomal dominant; AGM8 · AGM8 · autosomal agammaglobulinemia caused by mutation in TCF3 · TCF3 autosomal agammaglobulinemia
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