SERPIND1, serpin family D member 1, 3053

N. diseases: 60; N. variants: 5
Disease: Dysfibrinogenemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1260903
Disease: Dysfibrinogenemia
Dysfibrinogenemia 		0.010 Biomarker disease BEFREE Three families with antithrombin deficiency, 35 with protein C, 60 with protein S, four with plasminogen, four with heparin cofactor II, seven with combined deficiencies and one family with dysfibrinogenemia were included in the analysis. 9607121 1998