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5,620 results
  1. ... should. Factor X is one such coagulation factor. Factor X deficiency is often caused by an inherited defect in the factor X gene. This is called inherited factor X deficiency. Bleeding ranges from mild to severe depending on ...
  2. ... published></health-condition-summary><health-condition-summary ><name >Factor X deficiency</name><ghr-page >https://medlineplus.gov/genetics/condition/ ...
  3. ... Soulier Syndrome Factor V Deficiency Factor VII Deficiency Factor X Deficiency Factor XI Deficiency Factor XII Deficiency Factor XIII ... Resistance Afibrinogenemia Factor V Deficiency Factor VII Deficiency Factor X Deficiency Factor XI Deficiency Factor XII Deficiency Factor XIII ...
  4. ... Factor VII Deficiency C15.378.100.100.320 Factor X Deficiency C15.378.100.100.325 Factor XI Deficiency ... Factor VII Deficiency C15.378.100.141.320 Factor X Deficiency C15.378.100.141.325 Factor XI Deficiency ...
  5. ... Factor VII Deficiency C15.378.100.100.320...........................................Factor X Deficiency C15.378.100.100.325...........................................Factor XI Deficiency ...
  6. With bleeding disorders, there is a problem with blood clotting. It may be hard to stop the bleeding. Read about bleeding disorders and treatments. ... Normally, if ...
  7. ... topic><topic ><url >https://medlineplus.gov/genetics/condition/factor-x-deficiency</url><title >Factor X deficiency</title><other_names ><other_name >Congenital Stuart factor ...
  8. ... Prothrombin deficiency Factor V deficiency Factor VII deficiency Factor X deficiency Factor XI deficiency (hemophilia C) Glanzmann disease Hemophilia A ...
  9. ... Liang Z, Moons L, et al. Blood coagulation factor X deficiency causes partial embryonic lethality and fatal neonatal bleeding ... CA, Kadir RA. Pregnancy in women with congenital factor VII deficiency. Haemophilia. 2006 Jul; 12 :413–6. X-4, X-5. [ PubMed : 16834743 ] 940. Kushtagi P, ...
  10. ... Willebrand disease , factor V deficiency (OMIM 227400 ), or factor X deficiency (OMIM 227600 ); maternal warfarin use; or thrombophilia (most often heterozygosity for factor V Leiden mutation) (see Factor V Leiden Thrombophilia ). ...
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