OBO ID: DOID:0081143
Term Name: agammaglobulinemia 8B Search Ontology:
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:
OTHER agammaglobulinemia 8B PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TCF3 Agammaglobulinemia 8B, autosomal recessive 619824
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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