DOID:0080839 - X-linked warfarin sensitivity
Disease Ontology Definition:An inherited metabolic disorder that is characterized by bleeding complications when given warfarin for anticoagulation and that has_material_basis_in variation in the F9 gene on chromosome Xq27.
Xenbase Genes :
|OMIM:301052 - WARFARIN SENSITIVITY, X-LINKED|
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): inherited metabolic disorder (is_a)