PARK7, Parkinsonism associated deglycase, 11315

N. diseases: 161; N. variants: 15
Disease: Presenile dementia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		0.020 GeneticVariation disease BEFREE Atypical features in patients from Group I include, for example, a slower disease course (PARK2, PARK6, PARK7) or dementia (PARK1/4, PARK14). 19735092 2009
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		0.020 GeneticVariation disease BEFREE Our results suggest it is unlikely that haploinsufficiency in the DJ-1 gene imparts an increased risk for dementia. 15542239 2004