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Concept information

disease > hemopathy > coagulopathy > afibrinogenemia

Preferred term

afibrinogenemia  

Definition

  • Congenital afibrinogenemia is a rare, genetically inherited blood fibrinogen disorder in which the blood does not clot normally due to the lack of fibrinogen, a blood protein necessary for coagulation. (Wikipedia)

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URI

http://data.loterre.fr/ark:/67375/VH8-JBMTKFD7-J

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