Term Name: agammaglobulinemia 8B
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.
Ontology: Human Disease [DOID:0081143]   ( DOID:0081143 )

Relationships
is a type of: agammaglobulinemia autosomal recessive disease