F2, coagulation factor II, thrombin, 2147

N. diseases: 61; N. variants: 24
Disease: Hereditary factor II deficiency disease ×
Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0272317
Disease: Hereditary factor II deficiency disease
Hereditary factor II deficiency disease 		0.500 GermlineCausalMutation disease ORPHANET A novel congenital dysprothrombinemia leading to defective prothrombin maturation. 25242243 2014
CUI: C0272317
Disease: Hereditary factor II deficiency disease
Hereditary factor II deficiency disease 		0.500 GermlineCausalMutation disease ORPHANET Congenital prothrombin deficiency: an update. 23852823 2013