jejunal atresia Gene Set

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)
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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