Showing entry for Congenital malrotation of intestine



                               
General Disease Information
BXGD IdBXGD004406
Disease NameCongenital malrotation of intestine
Disease CUI IdC0221210
MeSH Codes C23   C16   C06  
Disease Class NamePathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id HP:0025031  
Human Phenotype Ontology TermAbnormality of the digestive system
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations