MAOB, monoamine oxidase B, 4129

N. diseases: 152; N. variants: 8
Disease: Sporadic Parkinson disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4511452
Disease: Sporadic Parkinson disease
Sporadic Parkinson disease 		0.040 GeneticVariation disease BEFREE The catechol-O-methyltransferase and monoamine oxidase B polymorphisms and levodopa therapy in the Iranian patients with sporadic Parkinson's disease. 23093014 2012
CUI: C4511452
Disease: Sporadic Parkinson disease
Sporadic Parkinson disease 		0.040 GeneticVariation disease BEFREE Association of monoamine oxidase B and catechol-O-methyltransferase polymorphisms with sporadic Parkinson's disease in an Iranian population. 23319194 2012
CUI: C4511452
Disease: Sporadic Parkinson disease
Sporadic Parkinson disease 		0.040 GeneticVariation disease BEFREE The combined haplotype of the MAOB G (G/G) and COMTHL genotype showed a fourfold increase (p < 0.05) in the risk of PD in female patients in this Polish population. 15753616 2005
CUI: C4511452
Disease: Sporadic Parkinson disease
Sporadic Parkinson disease 		0.040 Biomarker disease BEFREE The effect of monoamine oxidase B (MAOB) and catechol-O-methyltransferase (COMT) polymorphisms on levodopa therapy in patients with sporadic Parkinson's disease. 15355491 2004