COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
Disease: Acute onset pain ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0184567
Disease: Acute onset pain
Acute onset pain 		0.010 GeneticVariation phenotype BEFREE Specifically, SCD patients with the DRD3 homozygote genotypes, COMT 158 Met allele or Met/Met genotype, are more likely to have acute care utilization, an indicator of acute pain. 25102390 2014