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Summary Literature (0)
DOID:0081146 - common variable immunodeficiency 3

Disease Ontology Definition:A common variable immunodeficiency that has_material_basis_in homozygous or compound heterozygous mutation in the CD19 gene on chromosome 16p11.2.

Synonyms:

Xenbase Genes : cd19



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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): common variable immunodeficiency (is_a)