zollinger-ellison syndrome Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A syndrome that is haracterized by the development of a one or more tumors (gastrinoma) in the pancreas, duodenum, or both that secrete excessive levels of gastrin, a hormone that stimulates production of acid by the stomach. (Human Disease Ontology, DOID_0050782)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002044
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Genes

2 genes associated with the zollinger-ellison syndrome phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MEN1 multiple endocrine neoplasia I
PIEZO2 piezo-type mechanosensitive ion channel component 2