OBO ID: DOID:0080839
Term Name: X-linked warfarin sensitivity Search Ontology:
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)
OTHER X-linked warfarin sensitivity PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
F9 {Warfarin sensitivity} 301052
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None