Term Name:	common variable immunodeficiency 2
Synonyms:
Definition:	A common variable immunodeficiency that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the TNFRSF13B gene, which encodes the transmembrane activator and CAML interactor (TACI), on chromosome 17p11.2.
Ontology:	Human Disease [DOID:0081145]   ( DOID:0081145 )