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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, hemophilia C, Hereditary factor XI deficiency disease, plasma thromboplastin antecedent deficiency, Rosenthal's disease
Echinobase Genes
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Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee