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Results 1 - 10 of 35 for Congenital factor V deficiency
  1. ... s disease Parahemophilia Proaccelerin deficiency Genetic Testing Registry: Congenital factor V deficiency Congenital factor V deficiency National Organization for Rare ...
  2. ... Specific bleeding disorders include: Acquired platelet function defects Congenital platelet function defects Disseminated intravascular coagulation (DIC) Prothrombin deficiency Factor V deficiency Factor VII deficiency Factor X deficiency Factor ...
  3. Bleeding Disorders (National Library of Medicine)  
    Normally, if you get hurt, your body forms a blood clot to stop the bleeding. For blood to clot, your body needs cells called platelets and proteins known as clotting ...
  4. Blood Clots (National Library of Medicine)  
    What is a blood clot? A blood clot is a mass of blood that forms when platelets, proteins, and cells in the blood stick together. When you get hurt, your ...
  5. ... Testing Registry: Factor XIII, A subunit, deficiency of Congenital factor XIII deficiency ... Biswas A, Ivaskevicius V, Thomas A, Oldenburg J. Coagulation factor XIII deficiency. ...
  6. Rare Clotting Factor Deficiencies (World Federation of Hemophilia)  
    Bleeding Disorders/Specifics ... Bleeding Disorders ... Vitamin K/Learn More ... Vitamin K ... World Federation of Hemophilia
  7. Anemia is a condition in which the body does not have enough healthy red blood cells. Red blood cells provide oxygen to body tissues. ...
  8. Cerebral Venous Sinus Thrombosis (CVST) (Johns Hopkins Medicine)  
    Blood Clots/Specifics ... Blood Clots ... Johns Hopkins Medicine ... Cerebral venous sinus thrombosis occurs when a blood clot forms in the brain’s venous sinuses. This ...
  9. ... be altered in congenital leptin deficiency are unknown.Congenital leptin deficiency is a rare cause of obesity. Researchers are studying the factors involved in more common forms of obesity. LEP ...
  10. ... Glucose-6-phosphate dehydrogenase deficiency , also called G6PD deficiency Hereditary hemochromatosis Transthyretin amyloidosis Hereditary thrombophilia: prothrombin thrombophilia and factor V Leiden thrombophilia Alzheimer's disease Parkinson's disease ...
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