Showing entry for Perimembranous ventricular septal defect



                               
General Disease Information
BXGD IdBXGD007709
Disease NamePerimembranous ventricular septal defect
Disease CUI IdC0344925
MeSH Codes C16   C14  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id HP:0001626  
Human Phenotype Ontology TermAbnormality of the cardiovascular system
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations