Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Blood Coagulation Disorders
CUI: C0005779
Disease: Blood Coagulation Disorders
0.010 GeneticVariation BEFREE Our results suggest that, in addition to amyloid deposition, the G654A gelsolin gene defect causes altered gelsolin-mediated cellular mechanisms, which may contribute, e.g., to bleeding tendency in AGel amyloidosis patients. 10744159 2000