MYO7A, myosin VIIA, 4647

N. diseases: 104; N. variants: 194
Disease: Visual symptoms ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0422943
Disease: Visual symptoms
Visual symptoms 		0.010 GeneticVariation phenotype BEFREE This study examined the frequency of USH1 before the appearance of visual symptoms in Japanese deaf children by MYO7A mutation analysis. 23237960 2013