Showing entry for Congenital diaphragmatic hernia

General Disease Information
BXGD Id	BXGD004775
Disease Name	Congenital diaphragmatic hernia
Disease CUI Id	C0235833
MeSH Codes	C23   C16
Disease Class Name	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0003549   HP:0003011
Human Phenotype Ontology Term	Abnormality of connective tissue; Abnormality of the musculature
Disease Ontology Id	DOID:7
Disease Ontology Class Name	disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations