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agammaglobulinemia 8B
Summary
- 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.
- Super Class
- agammaglobulinemia autosomal recessive disease
External Links
- Disease Ontology
- DOID:0081143
- Mondo Disease Ontology
- OMIM
