COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
Disease: Dyspepsia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0013395
Disease: Dyspepsia
Dyspepsia 		0.010 GeneticVariation phenotype LHGDN The data suggest that the COMT genotype seems to influence the susceptibility of dyspepsia when it interacts with gender and age. 18705311 2008