YY1AP1, YY1 associated protein 1, 55249

N. diseases: 35; N. variants: 10
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 Identification of YY1AP1 mutations as a cause of FMD indicates that this condition can result from underlying genetic variants that significantly alter the phenotype of vascular smooth muscle cells. 27939641 2017