DYM, dymeclin, 54808

N. diseases: 155; N. variants: 31
Disease: Arteriopathic disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0852949
Disease: Arteriopathic disease
Arteriopathic disease 		0.010 GeneticVariation group BEFREE Human MYH11 gene mutations provide the first example of a direct change in a specific SMC protein leading to an inherited arterial disease. 16444274 2006