| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A developmental defect resulting in abnormal closure, or atresia of the tubular structure of the jejunum. (Human Phenotype Ontology, HP_0005235) |
| External Link | https://www.disgenet.org/browser/0/1/0/C0266175 |
| Similar Terms | |
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3 genes associated with the disease Jejunal Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
