Showing entry for WARFARIN SENSITIVITY (disorder)



                               
General Disease Information
BXGD IdBXGD017154
Disease NameWARFARIN SENSITIVITY (disorder)
Disease CUI IdC2608079
MeSH Codes C16   C18  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations