MYO7A, myosin VIIA, 4647

N. diseases: 104; N. variants: 194
Disease: Deafness, Autosomal Dominant 12 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1832187
Disease: Deafness, Autosomal Dominant 12
Deafness, Autosomal Dominant 12 		0.010 GeneticVariation disease BEFREE The critical regions for the recessive deafness locus DFNB2 and the dominant locus DFNA11, which were previously localized to the long arm of chromosome 11, do not overlap with the candidate interval of DFNA12. 9150164 1997