F7 deficiency is a rare blood clotting disorder which varies in severity between affected individuals. Patients may suffer from episodes of epistaxis, menorrhagia, hemarthrosis, intramuscular hematomas and hematuria.
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Coagulation defects, purpura and other haemorrhagic conditions
Autosomal recessive
13q34
F7 deficiency is a rare blood clotting disorder which varies in severity between affected individuals. Patients may suffer from episodes of epistaxis, menorrhagia, hemarthrosis, intramuscular hematomas and hematuria.