Search Ontology:
Human Disease

X-linked warfarin sensitivity

Term ID
DOID:0080839
Synonyms
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/
References
Ontology
Human Disease   ( DOID:0080839 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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