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Summary Literature (0)
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.

Synonyms:

Xenbase Genes :


OMIM:
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)