|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A developmental defect resulting in abnormal closure, or atresia of the tubular structure of the jejunum. (Human Phenotype Ontology, HP_0005235)|
|Downloads & Tools|
1 genes associated with the jejunal atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|RFX6||regulatory factor X, 6|