MAOB, monoamine oxidase B, 4129

N. diseases: 152; N. variants: 8
Disease: Motor disturbances ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2220255
Disease: Motor disturbances
Motor disturbances 		0.010 GeneticVariation phenotype BEFREE The aim of the study was to evaluate the effect of MAOB and COMT genetic polymorphism on effective daily dose of levodopa applied during the first 5 years of treatment, and to find out if a relationship exists between MAOB and COMT haplotypes and motor disturbances onset in PD patients treated with levodopa preparations. 15355491 2004