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Human Disease

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
Ontology
Human Disease   ( DOID:0081143 )
Relationships
is a type of
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Genes Involved
Zebrafish Models