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Metadata
ID	DOID:0081143
Name	agammaglobulinemia 8B
Definition	An agammaglobulinemia that is characterized by onset of recurrent infections in early childhood and that has_material_basis_in homozygous loss-of-function mutation in the TCF3 gene on chromosome 19p13. https://pubmed.ncbi.nlm.nih.gov/32384040/
Xrefs	MIM:619824
Parent Relationships	is_a agammaglobulinemia is_a autosomal recessive disease
Subclass Logical Relationships	existence starts during some Childhood onset has material basis in some autosomal recessive inheritance