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| Term | X-linked warfarin sensitivity | ID (Ontology) | DOID:0080839 (Human Disease) |
| 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. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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disease of metabolism__ genetic disease________| inherited metabolic disorder |__X-linked warfarin sensitivity 1 rec. |
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| Is a | inherited metabolic disorder | ||
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| MIM:301052 | |||