Search Ontology:
Human Disease
complement deficiency
- Term ID
- DOID:626
- Synonyms
-
- Complement deficiency disease
- 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. http://en.wikipedia.org/wiki/Complement_deficiency
- References
-
- ICD10CM:D84.1
- MESH:D000081208
- NCI:C4691
- SNOMEDCT_US_2023_03_01:191014008
- UMLS_CUI:C0272242
- Ontology
- Human Disease ( DOID:626 )
- is a type of
-
- has subtype
Other Pages
Genes Involved
Zebrafish Models