DOID:626 - complement deficiency
Disease Ontology Definition:A primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation.
Synonyms: Complement deficiency, Complement deficiency disease, Complement deficiency disease (disorder)
|MONDO:0003832 - complement deficiency|
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes : c2, c4a, c3, c5, c9, c6.2, c8a, c8b, c7, cfp, cfi, c6.1, c5.2
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): primary immunodeficiency disease (is_a)