Showing entry for Congenital chromosomal disease



                               
General Disease Information
BXGD IdBXGD000559
Disease NameCongenital chromosomal disease
Disease CUI IdC0008626
MeSH Codes C16  
Disease Class NameCongenital, 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