Sphincter of Oddi Dysfunction Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A gallbladder disease characterized by altered tonus of the sphincter of Oddi, disturbance in the coordination of contraction of the biliary ducts, and/or reduction in the speed of emptying of the biliary tree. (Human Disease Ontology, DOID_4140)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D046628
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Genes

2 genes/proteins associated with the disease Sphincter of Oddi Dysfunction from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
OPRM1 opioid receptor, mu 1 1.35098
OPRK1 opioid receptor, kappa 1 1.24687