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Concept information

disease > genetic disease > hereditary disease > genetic complement deficiency
disease > immunopathology > immune deficiency > genetic complement deficiency

Terme préférentiel

genetic complement deficiency  

Définition(s)

  • 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 (Wikidata)

Concept(s) générique(s)

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URI

http://data.loterre.fr/ark:/67375/VH8-B9PQQH41-T

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RDF/XML TURTLE JSON-LD Dernière modif. 14/05/2020