COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
Disease: Ablepharon ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266574
Disease: Ablepharon
Ablepharon 		0.010 GeneticVariation disease BEFREE Neurotypical (N = 91) adults were genotyped for the COMT Val158Met polymorphism, completed the Schizotypal Personality Questionnaire (SPQ), and had eyes open resting-state EEG recorded for 4 min. 30084963 2019