Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0403823
Disease: Asthenozoospermia
Asthenozoospermia
0.020 GeneticVariation disease BEFREE T26248G-transversion mutation in exon7 of the putative methyltransferase Nsun7 gene causes a change in protein folding associated with reduced sperm motility in asthenospermic men. 24384068 2015
CUI: C0403823
Disease: Asthenozoospermia
Asthenozoospermia
0.020 GeneticVariation disease BEFREE In the present study, we investigated the possible association between the genetic polymorphisms in exon7 of NSUN7 and asthenospermia in a Chinese Han population. 26345859 2015