CD2AP, CD2 associated protein, 23607

N. diseases: 113; N. variants: 14
Disease: Fibromuscular Dysplasia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0016052
Disease: Fibromuscular Dysplasia
Fibromuscular Dysplasia 		0.010 GeneticVariation disease BEFREE In a 3rd cohort (Ncases = 506, Ncontrols = 876) the genetic locus of one of these upstream disease drivers, CD2-associated protein (CD2AP), was independently validated as being associated with risk of having FMD (odds ratios  = 1.36; P = 0.0003). 31424497 2020