OBO ID: DOID:0080839 |
Term Name: | X-linked warfarin sensitivity | Search Ontology: | |
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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/ | ||
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Ontology: | Human Disease ( DOID:0080839 ) |
OTHER X-linked warfarin sensitivity PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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