CUI Disease Vocabulary Name in Vocabulary Code
C0272350 Dysfibrinogenemia, Congenital DO factor VII deficiency 2215
C0272350 Dysfibrinogenemia, Congenital DO factor V deficiency 2216
C0272350 Dysfibrinogenemia, Congenital ICD10CM Proaccelerin deficiency D68.2
C0272350 Dysfibrinogenemia, Congenital ICD10CM AC globulin deficiency D68.2
C0272350 Dysfibrinogenemia, Congenital ICD10CM Owren's disease D68.2
C0272350 Dysfibrinogenemia, Congenital ICD10CM Hypoproconvertinemia D68.2
C0272350 Dysfibrinogenemia, Congenital ICD10CM Dysfibrinogenemia (congenital) D68.2
C0272350 Dysfibrinogenemia, Congenital ICD10CM Congenital afibrinogenemia D68.2
C0272350 Dysfibrinogenemia, Congenital ICD10CM Deficiency of factor V [labile] D68.2
C0272350 Dysfibrinogenemia, Congenital ICD10CM Deficiency of factor VII [stable] D68.2
C0272350 Dysfibrinogenemia, Congenital ICD10CM Deficiency of factor X [Stuart-Prower] D68.2
C0272350 Dysfibrinogenemia, Congenital ICD10CM Deficiency of factor XII [Hageman] D68.2
C0272350 Dysfibrinogenemia, Congenital ICD10CM Deficiency of factor II [prothrombin] D68.2
C0272350 Dysfibrinogenemia, Congenital ICD10CM Deficiency of factor I [fibrinogen] D68.2
C0272350 Dysfibrinogenemia, Congenital MONDO familial dysfibrinogenemia 0014452
C0272350 Dysfibrinogenemia, Congenital MONDO familial hypodysfibrinogenemia 0016638
C0272350 Dysfibrinogenemia, Congenital MSH Dysfibrinogenemia, Congenital C562727
C0272350 Dysfibrinogenemia, Congenital OMIM DYSFIBRINOGENEMIA, CONGENITAL 616004
C0272350 Dysfibrinogenemia, Congenital OMIM HYPODYSFIBRINOGENEMIA, CONGENITAL 616004
C0272350 Dysfibrinogenemia, Congenital ORDO Familial hypodysfibrinogenemia 248408
C0272350 Dysfibrinogenemia, Congenital ORDO Familial dysfibrinogenemia 98881