F2, coagulation factor II, thrombin, 2147

N. diseases: 61; N. variants: 24
Disease: Factor II deficiency ×
Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3203356
Disease: Factor II deficiency
Factor II deficiency 		0.400 GermlineCausalMutation disease ORPHANET A novel congenital dysprothrombinemia leading to defective prothrombin maturation. 25242243 2014
CUI: C3203356
Disease: Factor II deficiency
Factor II deficiency 		0.400 GermlineCausalMutation disease ORPHANET Congenital prothrombin deficiency: an update. 23852823 2013