COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
Disease: Fatigue ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0015672
Disease: Fatigue
Fatigue 		0.030 GeneticVariation phenotype BEFREE In this pilot exploratory study, the primary aim was to determine whether genetic polymorphisms of tryptophan hydroxylase ( TPH1/TPH2), serotonin reuptake transporter ( SERT), or catechol-O-methyltransferase ( COMT) are associated with fatigue in women with IBS. 30309244 2019
CUI: C0015672
Disease: Fatigue
Fatigue 		0.030 GeneticVariation phenotype BEFREE Catechol-O-methyltransferase genotype (Val158met) modulates cancer-related fatigue and pain sensitivity in breast cancer survivors. 21898113 2012
CUI: C0015672
Disease: Fatigue
Fatigue 		0.030 GeneticVariation phenotype BEFREE Participants (n=63) completed self-report questionnaires and had COMT genotype determined before performing a standardized fatigue protocol to induce delayed onset muscle soreness. 18936597 2008