MYO6, myosin VI, 4646

N. diseases: 66; N. variants: 22
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0395971
Disease: Dominant sensorineural hearing loss
Dominant sensorineural hearing loss
0.020 GeneticVariation disease BEFREE Clinical and audiological examination was done in 2 Belgian families with autosomal dominant sensorineural hearing loss (SNHL) linked to DFNA22. 19893302 2010
CUI: C0395971
Disease: Dominant sensorineural hearing loss
Dominant sensorineural hearing loss
0.020 GeneticVariation disease BEFREE Linkage analysis revealed linkage to locus DFNA22 in two Belgian families 1 and 2 with autosomal dominant sensorineural hearing loss. 18212818 2008