Disease-gene associations mined from literature

Human genes for congenital diaphragmatic hernia

Congenital diaphragmatic hernia [DOID:3827]

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:  congenital diaphragmatic hernia,  DOID:3827,  Diaphragmatic Hernia

Linkouts:  OMIM #1 #2 #3 #4