Showing entry for Trisomy 11



                               
General Disease Information
BXGD IdBXGD008786
Disease NameTrisomy 11
Disease CUI IdC0432409
MeSH Codes C23   C16  
Disease Class NamePathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations