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DOID:0081149 - common variable immunodeficiency 6
Disease Ontology Definition:A common variable immunodeficiency that has_material_basis_in homozygous mutation in the CD81 gene on chromosome 11p.
Synonyms:
Xenbase Genes : cd81
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)