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Summary Literature (0)
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 - foregut duodenum mesentery

MIM:
MIM:142340 - DIAPHRAGMATIC HERNIA, CONGENITAL
MIM:222400 - DIAPHRAGMATIC HERNIA 2; DIH2
MIM:610187 - DIAPHRAGMATIC HERNIA 3; DIH3

Other Model Organisms: Alliance, 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)