Showing entry for Acquired von Willebrand's disease



                               
General Disease Information
BXGD IdBXGD006357
Disease NameAcquired von Willebrand's disease
Disease CUI IdC0272362
MeSH Codes C16   C15  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:7  
Disease Ontology Class Namedisease of anatomical entity
Disorder Network disorder-protein-compound-food associations