Showing entry for Foramen Ovale, Patent

General Disease Information
BXGD Id	BXGD001067
Disease Name	Foramen Ovale, Patent
Disease CUI Id	C0016522
MeSH Codes	C16   C14
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0001626
Human Phenotype Ontology Term	Abnormality of the cardiovascular system
Disease Ontology Id	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations