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Summary Literature (0)
DOID:0081152 - common variable immunodeficiency 10


Disease Ontology Definition:A common variable immunodeficiency that has_material_basis_in heterozygous mutation in the NFKB2 gene on chromosome 10q24.

Synonyms:

Xenbase Genes : nfkb2



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

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