Showing entry for Congenital hernia of foramen of Morgagni

General Disease Information
BXGD Id	BXGD005567
Disease Name	Congenital hernia of foramen of Morgagni
Disease CUI Id	C0265699
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
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations