MIDN, midnolin, 90007

N. diseases: 3; N. variants: 0
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.020 Biomarker disease BEFREE In the present study, we aimed to replicate the genetic association between MIDN and PD in a large British population cohort. 31588691 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.020 AlteredExpression disease BEFREE Midnolin is a novel regulator of parkin expression and is associated with Parkinson's Disease. 28724963 2017