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38 results
  1. ... copy of the mutated gene and have partial factor XI deficiency; they rarely show severe signs and symptoms of the condition. In some families, this condition ...
  2. ... people with this disorder have few if any symptoms. The most common feature of factor XI deficiency is prolonged bleeding after trauma or surgery, especially ...
  3. ... mild or moderate hemophilia B. A specific factor XI clotting assay establishes the diagnosis. Factor XII (OMIM 234000 ), prekallikrein (OMIM 612423 ), or high molecular-weight kininogen deficiencies (OMIM 228960 ) do not cause clinical bleeding but ...
  4. ... on official, secure websites. Explore the signs and symptoms, genetic cause, and inheritance pattern of various health conditions. ... F10 deficiency, see Factor X deficiency F11 deficiency, see Factor XI deficiency F7 deficiency, see Factor VII deficiency FA, ...
  5. ... Romano-Ward syndrome Rosacea Rosenthal factor deficiency, see Factor XI deficiency Rosenthal syndrome, see Factor XI deficiency Rosenthal's disease, see Factor XI deficiency Rothmund-Thomson ...
  6. ... see Multiple myeloma Plasma thromboplastin antecedent deficiency, see Factor XI deficiency Plasminogen activator inhibitor type 1 deficiency, see Complete ...
  7. ... topic><topic ><url >https://medlineplus.gov/genetics/condition/factor-xi-deficiency</url><title >Factor XI deficiency</title><other_names ><other_name >F11 deficiency</other_ ...
  8. ... Hereditary hemochromatosis Haemophilia, see Hemophilia Haemophilia C, see Factor XI deficiency Hailey-Hailey disease Hajdu-Cheney syndrome HAL deficiency, ...
  9. ... 4 NP_055059.2 Shi et al [2017] Factor XI deficiency (OMIM 612416 ) AD AR F11 c.403G>T ... 73. [ PubMed : 23990280 ] Gomez K, Bolton-Maggs P. Factor XI deficiency. Haemophilia. 2008; 14 :1183–9. [ PubMed : 18312365 ] Horani ...
  10. ... V deficiency Factor VII deficiency Factor X deficiency Factor XI deficiency (hemophilia C) Glanzmann disease Hemophilia A Hemophilia B Idiopathic thrombocytopenic purpura (ITP) Von Willebrand disease (types I, II, and III)
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