Summary Literature (0)

DOID:2229 - factor XI deficiency

Disease Ontology Definition: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: Congenital factor XI deficiency, Hereditary factor XI deficiency disease, Rosenthal's disease, hemophilia C, plasma thromboplastin antecedent deficiency,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012897 - congenital factor XI deficiency

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee