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Metadata
ID	DOID:0081140
Name	agammaglobulinemia 8A
Definition	An agammaglobulinemia that has_material_basis_in heterozygous dominant-negative mutation in the TCF3 gene on chromosome 19p13. https://pubmed.ncbi.nlm.nih.gov/32384040/
Xrefs	MIM:616941
Parent Relationships	is_a agammaglobulinemia is_a autosomal dominant disease