pancreatic calcification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of abnormal calcium deposition lesions in the pancreas. (Human Phenotype Ontology, HP_0005213)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005213
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
PRSS1 protease, serine, 1 (trypsin 1)
SPINK1 serine peptidase inhibitor, Kazal type 1