Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4629
Gene Symbol: MYH11
MYH11
CUI: C0852949
Disease: Arteriopathic disease
Arteriopathic disease 		0.010 GeneticVariation 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