| Dataset | GAD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A physical disorder characterized by a defect in the development of the abdominal wall muscles, resulting in the intestines, liver and other organs to remain outside of the abdomen in a sac. (Human Disease Ontology, DOID_0060327) |
| Similar Terms | |
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4 genes associated with the disease omphalocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
