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Summary Literature (1)
DOID:3827 - congenital diaphragmatic hernia

Disease Ontology Definition:A diaphragm disease characterized by the lack of development of all or part of the diaphragm, which results in an abnormal opening that allows the stomach and intestines to move into the chest cavity and crowd the heart and lungs.

Synonyms: Diaphragmatic Hernia,

Xenbase Genes : zfpm2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0005711 - congenital diaphragmatic hernia


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): diaphragm disease (is_a), physical disorder (is_a)