X-Linked Warfarin Sensitivity
Disease ID: disease_node_17533
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| Dbxref | MIM:301052 |
|---|---|
| Subclassof | DOID_655 |
| Data Source | DOID |
| Doid Label | X-linked warfarin sensitivity |
| Doid Description | 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. |
| Disease Node Id | disease_node_17533 |
| Doid Id | DOID_0080839 |
| Label | X-Linked Warfarin Sensitivity |
- Outgoing r'ship
SUBCLASS_OFto/from Metabolism, Inborn Errors(ID:disease_node_5171) (Disease)