COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
Disease: Vertigo ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0042571
Disease: Vertigo
Vertigo 		0.010 GeneticVariation phenotype BEFREE In the ED in the hours after MVC, individuals with a COMT pain vulnerable genotype were more likely to report moderate-to-severe musculoskeletal neck pain (76 versus 41%, RR = 2.11 (1.33-3.37)), moderate or severe headache (61 versus 33%, RR = 3.15 (1.05-9.42)), and moderate or severe dizziness (26 versus 12%, RR = 1.97 (1.19-3.21)). 20688576 2011