Disease: Congenital hypofibrinogenemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2584774
Disease: Congenital hypofibrinogenemia
Congenital hypofibrinogenemia 		0.300 Biomarker disease CTD_human BSEP inhibition: in vitro screens to assess cholestatic potential of drugs. 22120137 2012