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Prothrombin deficiency
- Prothrombin deficiency is a bleeding disorder that slows the blood clotting process. People with this condition often experience ...
- ... the F2 gene have been found to cause prothrombin deficiency, a bleeding disorder that slows the clotting process. ... of the variants that are known to cause prothrombin deficiency eliminate prothrombin function. Researchers believe that some prothrombin ...
- ... is not inherited. F7 deficiency Hypoproconvertinemia Proconvertin deficiency Prothrombin conversion accelerator deficiency Serum prothrombin conversion accelerator deficiency Genetic Testing Registry: ...
- ... Hoek B, Rosendaal FR. Factor V Leiden mutation, prothrombin gene mutation, and deficiencies in coagulation inhibitors associated with Budd-Chiari syndrome ...
- ... Glucose-6-phosphate dehydrogenase deficiency , also called G6PD deficiency Hereditary hemochromatosis Transthyretin amyloidosis Hereditary thrombophilia: prothrombin thrombophilia and factor V Leiden thrombophilia Alzheimer's ...
- ... Serum Prothrombin Conversion Accelerator, Proconvertin, Stable Factor, ... Deficiency Study Group. Factor VII deficiency: clinical manifestation of ...
- ... in conversion of an important coagulation protein called prothrombin to its active form, ... called factor XI deficiency. This disorder, while usually mild, can cause nosebleeds, ...
- ... factors to convert an important coagulation protein called prothrombin to its active form, ... factor X deficiency. This disorder commonly causes nosebleeds, easy bruising, bleeding ...
