familial dysfibrinogenemia https://github.com/monarch-initiative/mondo/issues/4521 https://rarediseases.info.nih.gov/diseases/2004/dysfibrinogenemia https://www.malacards.org/card/dysfibrinogenemia_congenital https://www.malacards.org/card/familial_dysfibrinogenemia GARD:0002004 congenital dysfibrinogenemia MEDGEN:82901 dysfibrinogenemia, familial UMLS:C0272350 NCIT:C131659 hypodysfibrinogenemia OMIM:616004 dysfibrinogenemia MONDO:0014452 Orphanet:98881 SCTID:111589005 Familial dysfibrinogenemia is a coagulation disorder characterized by a bleeding tendency due to a functional anomaly of circulating fibrinogen. ICD9:286.3 familial dysfibrinogenemia congenital fibrinogen deficiency