Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders
0.430 Biomarker group HPO
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders
0.430 GeneticVariation group BEFREE This review will address Mn transport proteins, the newly discovered SLC30A10 mutations and their implications to Parkinsonism and Mn regulation. 23357421 2013
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders
0.430 GeneticVariation group BEFREE Our results provide novel insights into the mechanisms involved in the onset of a familial form of parkinsonism and highlight the possibility of using enhanced Mn efflux as a therapeutic strategy for the potential management of Mn-induced parkinsonism, including that occurring as a result of mutations in SLC30A10. 25319704 2014
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders
0.430 Biomarker group CTD_human Manganese-Induced Parkinsonism Is Not Idiopathic Parkinson's Disease: Environmental and Genetic Evidence. 26220508 2015
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders
0.430 GeneticVariation group BEFREE SLC30A10 Mutation Involved in Parkinsonism Results in Manganese Accumulation within Nanovesicles of the Golgi Apparatus. 30272946 2019