Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.420 Biomarker disease CTD_human We found significant previously unidentified signals (P < 5 × 10(-8)) associated with PSP risk at STX6, EIF2AK3 and MOBP. 21685912 2011
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.420 GeneticVariation disease GWASCAT We found significant previously unidentified signals (P < 5 × 10(-8)) associated with PSP risk at STX6, EIF2AK3 and MOBP. 21685912 2011
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.420 GeneticVariation disease BEFREE Meta-analysis revealed highly significant associations for PSP risk alleles of rs8070723 and rs1768208 with higher LRRC37A4 and MOBP brain levels, respectively. 27115769 2016
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.420 GeneticVariation disease GWASDB We found significant previously unidentified signals (P < 5 × 10(-8)) associated with PSP risk at STX6, EIF2AK3 and MOBP. 21685912 2011
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.420 GeneticVariation disease BEFREE We identify new CBD susceptibility loci and show that CBD and PSP share a genetic risk factor other than MAPT at 3p22 MOBP (myelin-associated oligodendrocyte basic protein). 26077951 2015
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.420 GeneticVariation disease GWASCAT Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases. 30089514 2018