agammaglobulinemia 8B

Term ID

DOID:0081143

Synonyms

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/

References

• OMIM:619824

Ontology

Human Disease   ( DOID:0081143 )