ELOVL7, ELOVL fatty acid elongase 7, 79993

N. diseases: 13; N. variants: 4
Disease: Multiple System Atrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0393571
Disease: Multiple System Atrophy
Multiple System Atrophy 		0.100 GeneticVariation phenotype GWASCAT A genome-wide association study in multiple system atrophy. 27629089 2016