- ... 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 ...
- ... 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 ...
- ... Hemophilia B XL Clinically indistinguishable from hemophilia A Diagnosis is based on factor IX clotting activity <40%. F11 Factor XI deficiency (OMIM 612416 ) AR AD Compound heterozygous & homozygous persons ...
- ... have activity <1%-15%. 1 A specific factor XI clotting assay establishes the diagnosis. F12 KLKB1 KNG1 Factor XII (OMIM 234000 ), prekallikrein (OMIM 612423 ), or high molecular-weight kininogen deficiencies (OMIM 228960 ) AR Not assoc w/clinical bleeding ...
- ... 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, ...
- ... usually do not experience abnormal bleeding or other symptoms. Factor XII deficiency is typically discovered during routine blood testing because ...
- ... COL11A1 gene are among many genetic and environmental factors that likely influence this complex disease. COBA1_HUMAN COLL6 collagen type XI alpha 1 collagen XI, alpha-1 polypeptide collagen, ...
- ... in women with von Willebrand's disease or factor XI deficiency. Br J Obstet Gynaecol. 1998 Mar; 105 :314– ... labor is not mandatory for women with severe factor XI deficiency. Blood Coagul Fibrinolysis. 2005 Jan; 16 :37–41. ...
- ... 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 ...
- ... see Multiple myeloma Plasma thromboplastin antecedent deficiency, see Factor XI deficiency Plasminogen activator inhibitor type 1 deficiency, see Complete ...
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