congenital diaphragmatic hernia Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description 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. (Human Disease Ontology, DOID_3827)
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Genes

2 genes involed in the disease congenital diaphragmatic hernia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
GATA4 GATA binding protein 4
ZFPM2 zinc finger protein, FOG family member 2