| Svéd | Magyar orvosi |
|---|
| faktor V | V-ös faktor [serum proaccelerin]infoFactor V, serum proaccelerin, a protein of the coagulation system |
| faktor V-brist | V-ös faktorhiányinfoFactor V deficiency, a bleeding disorder that is passed down through families |
| faktor VI | VI-os faktor [véralvadás egyik tényezője] [serum accelerin]infoFactor VI, intrinsic factor a glycoprotein secreted by the parietal cells of the gastric glands, necessary for the absorption of cyanocobalamin |
| faktor VI-bris | VI-os faktorhiányinfoFactor V deficiency, deficiency of absorption of cyanocobalamin |
| faktor VII | VII-es faktorinfoFactor VII, FVII, proconvertin, a coagulation factor formed in the kidney under the influence of vitamin K |
| faktor VII-brist | VII-es faktorhiányinfoFactor VII deficiency, Alexander's disease, a type of clotting disorder |
| faktor VIII | VIII-as faktorinfoFactor VIII, antihemophilic factor, an essential blood-clotting protein |
| faktor VIII-brist | VIII-as faktorhiányinfoFactor VIII deficiency, hemophilia A |
| avsaknad av faktor VIII infoklassisk hemofili | factor VIII hiány [classical hemophilia]infohemophilia A, classical hemophilia, classic hemophilia, factor VIII deficiency |
| human koagulationsfaktor VII | humán VII. véralvadási faktor [Factor VII coagulationis humanus]infohuman factor VII, coagulation factor VII, one of the proteins that causes blood to clot in the coagulation cascade, and in humans is coded for by the gene F7 |
| human koagulationsfaktor VIII | humán VIII. véralvadási faktor [Factor VIII coagulationis humanus]infohuman factor VIII, antihemophilic factor, the protein that is deficient or defective in patients with classical hemophilia and Von Willebrand syndrome |
| medfödd faktor VIII störning | kongenitális VIII-as faktor rendellenesség [f.r.]infocongenital factor VIII disorder, hemophilia A, a hereditary bleeding disorder caused by a lack of blood clotting factor VIII. Without enough factor VIII, the blood cannot clot properly to control bleeding |
