Showing entry for Hereditary factor XII deficiency disease



                               
General Disease Information
BXGD IdBXGD006349
Disease NameHereditary factor XII deficiency disease
Disease CUI IdC0272334
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:630  
Disease Ontology Class Namegenetic disease
Disorder Network disorder-protein-compound-food associations