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Complement component 3 deficiency

Disease definition

Complement component 3 deficiency is a rare, genetic, primary immunodeficiency characterized by susceptibility to infection (mainly by gram negative bacteria) due to extremely low C3 plasma levels. Patients typically present recurrent episodes of sinusitis, tonsillitis, and/or otitis, as well as upper and lower respiratory tract infections (including pneumonia) and skin infections, such as erythema multiforme. Autoimmune disease resembling systemic lupus erythematosus and mesangiocapillary or membranoproliferative glomerulonephritis may develop, resulting in renal failure.


Classification level: Disorder
  • Synonym(s):
    • C3 deficiency
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: Childhood
  • ICD-10: D84.1
  • OMIM: 613779
  • UMLS: C3151071
  • MeSH: -
  • GARD: 10625  10626  9521  9526
  • MedDRA: -

Additional information

Further information on this disease

Specialised Social Services

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