| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A developmental defect resulting in abnormal closure, or atresia of the tubular structure of the jejunum. (Human Phenotype Ontology, HP_0005235) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0005235 |
| Similar Terms | |
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1 genes associated with the jejunal atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| RFX6 | regulatory factor X, 6 |
