Showing entry for Von willebrand factor, deficiency

General Disease Information
BXGD Id	BXGD017904
Disease Name	Von willebrand factor, deficiency
Disease CUI Id	C2930849
MeSH Codes	C16   C15
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations