APOE, apolipoprotein E, 348

N. diseases: 1049; N. variants: 62
Disease: Visuospatial deficit ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2921138
Disease: Visuospatial deficit
Visuospatial deficit 		0.010 GeneticVariation phenotype BEFREE This specific pattern of visuospatial deficit was found to be independent of apolipoprotein E genotype and closely resembles what has recently been termed vascular mild cognitive impairment, in turn associated with subtle sub-cortical vascular changes. 20858969 2010