OBO ID: DOID:0081143 |
Term Name: | agammaglobulinemia 8B | Search Ontology: | |
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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/ | ||
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Ontology: | Human Disease ( DOID:0081143 ) |
OTHER agammaglobulinemia 8B PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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