Showing entry for Peutz-Jeghers Syndrome



                               
General Disease Information
BXGD IdBXGD002297
Disease NamePeutz-Jeghers Syndrome
Disease CUI IdC0031269
MeSH Codes C16   C06   C04   C17  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:7   DOID:14566  
Disease Ontology Class Namedisease of anatomical entity; disease of cellular proliferation
Disorder Network disorder-protein-compound-food associations