MYO7A, myosin VIIA, 4647

N. diseases: 104; N. variants: 194
Disease: Low frequency deafness ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0271514
Disease: Low frequency deafness
Low frequency deafness 		0.020 GeneticVariation disease BEFREE Here, we present the clinical, genetic and molecular characteristics of two large Chinese DFNA11 families with either high- or low-frequency hearing loss. 21150918 2011
CUI: C0271514
Disease: Low frequency deafness
Low frequency deafness 		0.020 GeneticVariation disease BEFREE Unusual phenotypes in autosomal dominant forms of deafness, include low frequency hearing loss in DFNA1 (HDIA1) and DFNA6/14/38 (WFS1), mid-frequency hearing loss in DFNA8/12 (TECTA), DFNA13 (COL11A2) and vestibular symptoms and signs in DFNA9 (COCH) and sometimes in DFNA11 (MYO7A). 12324385 2002