Showing entry for Situs ambiguus



                               
General Disease Information
BXGD IdBXGD005705
Disease NameSitus ambiguus
Disease CUI IdC0266642
MeSH Codes C16   C15   C14  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id HP:0001507  
Human Phenotype Ontology TermGrowth abnormality
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations