OBO ID: DOID:626
Term Name: complement deficiency Search Ontology:
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 )
OTHER complement deficiency PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None