MYO7A, myosin VIIA, 4647

N. diseases: 104; N. variants: 194
Disease: Deaf-Blind Syndromes ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1955858
Disease: Deaf-Blind Syndromes
Deaf-Blind Syndromes 		0.010 GeneticVariation disease BEFREE 4), has been localized to the same chromosomal region, 11q14, as one of the loci, USH1B, underlying the recessive deaf-blind syndrome. 9171832 1997