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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 (disorder),
Echinobase Genes
:
c3
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
primary immunodeficiency disease (is_a)