|OBO ID: DOID:0080839|
|Term Name:||X-linked warfarin sensitivity||Search 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. https://pubmed.ncbi.nlm.nih.gov/29450643/|
|Ontology:||Human Disease (DOID:0080839)|
|is a type of:||
OTHER X-linked warfarin sensitivity PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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