Visualize Submit Comment
Metadata
ID DOID:0080839
Name X-linked warfarin sensitivity
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.
https://pubmed.ncbi.nlm.nih.gov/29450643/
Xrefs

OMIM:301052

Parent Relationships

is_a inherited metabolic disorder

Add an item to the term tracker