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Summary Literature (0)
DOID:0081140 - agammaglobulinemia 8A

Disease Ontology Definition:An agammaglobulinemia that has_material_basis_in heterozygous dominant-negative mutation in the TCF3 gene on chromosome 19p13.

Synonyms:

Xenbase Genes : tcf3



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): agammaglobulinemia (is_a), autosomal dominant disease (is_a)