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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, Complement deficiency disease (disorder)
Xenbase Genes
:
c2,
c4a,
c3,
c5,
c9,
c6.2,
c8a,
c8b,
c7,
cfp,
cfi,
c6,
c5.2
| MONDO:0003832 - esophagus muscle |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
primary immunodeficiency disease (is_a)