Showing entry for Congenital digestive system anomalies

General Disease Information
BXGD Id	BXGD005607
Disease Name	Congenital digestive system anomalies
Disease CUI Id	C0266015
MeSH Codes	C16   C06
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0025031
Human Phenotype Ontology Term	Abnormality of the digestive system
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations