Showing entry for Umbilical hernia



                               
General Disease Information
BXGD IdBXGD001317
Disease NameUmbilical hernia
Disease CUI IdC0019322
MeSH Codes C23   C16   C13  
Disease Class NamePathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id HP:0025031   HP:0003549  
Human Phenotype Ontology TermAbnormality of the digestive system; Abnormality of connective tissue
Disease Ontology Id DOID:7   DOID:0080015  
Disease Ontology Class Namedisease of anatomical entity; physical disorder
Disorder Network disorder-protein-compound-food associations