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DOID:0081150 - common variable immunodeficiency 7
Disease Ontology Definition:A common variable immunodeficiency that has_material_basis_in compound heterozygous mutation in the CD21 gene (CR2) on chromosome 1q32.
Synonyms:
Xenbase Genes

MIM:614699 - IMMUNODEFICIENCY, COMMON VARIABLE, 7; CVID7 |
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)