MYH14, myosin heavy chain 14, 79784

N. diseases: 64; N. variants: 9
Disease: Congenital clubfoot ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.010 GeneticVariation disease BEFREE In this study, we hypothesized that a mutation in an embryonic or perinatal myosin gene could be associated with congenital idiopathic clubfoot. 20357587 2010