F10, coagulation factor X, 2159

N. diseases: 228; N. variants: 44
Disease: Hereditary factor II deficiency disease ×
Source: ALL
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 		0.010 GeneticVariation disease BEFREE Prothrombin San Antonio: a single amino acid substitution at a factor Xa activation site (Arg320 to His) results in dysprothrombinemia. 10627484 2000