rs6025, F5

N. diseases: 43
Disease: Acquired porencephaly ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Acquired porencephaly
CUI: C0151860
Disease: Acquired porencephaly
0.010 GeneticVariation BEFREE The Arg506 to Gln mutation, factor V, protein C, protein S, antithrombin, antiphospholipid antibodies and lipoprotein (a) (Lp(a)) were retrospectively measured in neonates and children with porencephaly (n = 24). 9577282 1998