Showing entry for COWDEN-LIKE SYNDROME (disorder)



                               
General Disease Information
BXGD IdBXGD017334
Disease NameCOWDEN-LIKE SYNDROME (disorder)
Disease CUI IdC2676500
MeSH Codes C16   C04   C18  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; 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