SERPIND1, serpin family D member 1, 3053

N. diseases: 60; N. variants: 5
Disease: Factor V Leiden mutation ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		0.010 GeneticVariation disease BEFREE The heparin cofactor II gene alteration was associated with, in one patient, the factor V Leiden mutation and, in the other, type I protein C deficiency. 8902986 1996