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MIRAGE
X-linked warfarin sensitivity

Summary
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.
Super Class
inherited metabolic disorder
Disease Ontology
DOID:0080839
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2158 F9 coagulation factor IX
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P00740 Coagulation factor IX
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 8, 2025