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Disease Ontology Browser
complement deficiency (DOID:626)
Alliance: disease page
Synonyms: Complement deficiency disease
Alt IDs: ICD10CM:D84.1, MESH:D000081208, NCI:C4691, UMLS_CUI:C0272242
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.

Disease References using Mouse Models (5)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory