WRN, WRN RecQ like helicase, 7486

N. diseases: 172; N. variants: 89
Disease: Atherosclerosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.120 GeneticVariation disease BEFREE We report on a familial case of atypical Werner syndrome (a progeroid syndrome with Werner syndrome phenotype but without typical RECQL2 mutation) presenting with acute ischemic cerebral disease or peripheral artery disease associated with diffuse atherosclerosis, attributable to transmission of a novel LMNA mutation. 19095983 2009
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.120 GeneticVariation disease BEFREE Previous studies have identified specific polymorphisms within WRN that may modulate the risk of atherosclerosis. 11186893 2000
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.120 Biomarker disease HPO