Disease-gene associations mined from literature

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 ...

Linkouts:  OMIM