/agammaglobulinemia 8, autosomal dominant

agammaglobulinemia 8, autosomal dominant

Rare Disease

MONDO:0014840

Also Known As

AGM8TCF3 autosomal agammaglobulinemiaagammaglobulinemia 8, autosomal dominantagammaglobulinemia 8, autosomal dominant; AGM8autosomal agammaglobulinemia caused by mutation in TCF3agammaglobulinemia, autosomal dominant, due to TCF3 defect

Definition

Any autosomal agammaglobulinemia in which the cause of the disease is a mutation in the TCF3 gene.

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Associated Genes

TCF3 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:616941 ↗

GARD

GARD:16171 ↗

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