Search Ontology:
Human Disease
agammaglobulinemia 8B
- Term ID
- DOID:0081143
- Synonyms
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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/
- References
- Ontology
- Human Disease ( DOID:0081143 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models