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Results 1 - 10 of 23 for Inherited blood coagulation disorder
  1. ... factor X deficiency. Reduced quantity or function of coagulation factor X prevents blood from clotting normally, causing episodes of abnormal bleeding that can be severe.A non-inherited form of the disorder, called acquired factor X deficiency, is more common ...
  2. ... a group of disorders classified as rare bleeding disorders. ... chemical reactions that forms blood clots in response to injury. These mutations reduce ...
  3. Factor V Leiden thrombophilia is an inherited disorder of blood clotting. Factor V Leiden is the name of a specific gene mutation that results in thrombophilia, which is an ...
  4. ... a rare bleeding disorder. Researchers have identified an inherited form and a less severe form that is ... a person's lifetime.Signs and symptoms of inherited factor XIII deficiency begin soon after birth, usually ...
  5. ... people who have protein S deficiency and another inherited blood clotting disorder may have a higher risk ... kidney disorders. PROS1 Protein S deficiency is typically inherited in an autosomal dominant pattern, which means one ...
  6. ... on PubMed Asselta R, Tenchini ML, Duga S. Inherited defects of coagulation factor V: the hemorrhagic side. ... Sharifian R, Peyvandi F, Mannucci PM. Symptoms of inherited factor V deficiency in 35 Iranian patients. Br ...
  7. ... of the condition. F5 Factor V deficiency is inherited in an autosomal recessive pattern, which means both ... Sharifian R, Peyvandi F, Mannucci PM. Symptoms of inherited factor V deficiency in 35 Iranian patients. Br ...
  8. ... the condition.In some families, this condition is inherited in an autosomal dominant pattern, which means one ... acquired form of factor XI deficiency is not inherited and does not run in families. F11 deficiency ...
  9. ... known as acquired hemophilia, is not caused by inherited gene variants. This rare condition is characterized by ... F8 F9 Hemophilia A and hemophilia B are inherited in an X-linked recessive pattern. The genes ...
  10. ... in people without other serious medical problems, certain inherited muscle diseases (including central core disease, multiminicore disease, ... under study. CACNA1S RYR1 Malignant hyperthermia susceptibility is inherited in an autosomal dominant pattern, which means one ...
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