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 )
Relationships
is a type of
has subtype
Other Pages
Genes Involved
Zebrafish Models