Human genes for factor XI deficiency
Factor XI deficiency [DOID:2229]
A blood coagulation disease that is characterized by deficiency of factor XI clotting factor and mild prolonged bleeding, especially of mucosal sites following trauma, and has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation of the coagulation factor XI gene of chromosome 4q35.2.
Synonyms: factor XI deficiency, DOID:2229, factor XI deficiencies, Congenital factor XI deficiency, hemophilia C ...
Linkouts: OMIM