Human genes for factor XI deficiency
Factor XI deficiency [DOID:2229]
Haemophilia C is a mild form of haemophilia affecting both sexes. However, it predominantly occurs in Jews of Ashkenazi descent. It is the fourth most common coagulation disorder after von Willebrand's disease and haemophilia A and B. In the USA it is thought to affect 1 in 100,000 of the adult population, making it 10% as common as haemophilia A.
Synonyms: factor XI deficiency, DOID:2229, Congenital factor XI deficiency, Hereditary factor XI deficiency disease (disorder), Rosenthal's disease ...