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DOID:0081147 - common variable immunodeficiency 4
Disease Ontology Definition:A common variable immunodeficiency that has_material_basis_in homozygous mutation in the BAFFR gene (TNFRSF13C), which encodes the B-cell activating factor receptor, on chromosome 22q13.
Synonyms:
Xenbase Genes

MIM:613494 - IMMUNODEFICIENCY, COMMON VARIABLE, 4; CVID4 |
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)