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agammaglobulinemia 8A
Summary
- Definition
- An agammaglobulinemia that has_material_basis_in heterozygous dominant-negative mutation in the TCF3 gene on chromosome 19p13.
- Super Class
- agammaglobulinemia autosomal dominant disease
External Links
- Disease Ontology
- DOID:0081140
- Mondo Disease Ontology
- OMIM
