Showing entry for Congenital von Willebrand's disease



                               
General Disease Information
BXGD IdBXGD008199
Disease NameCongenital von Willebrand's disease
Disease CUI IdC0398610
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   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations