MYH14, myosin heavy chain 14, 79784

N. diseases: 64; N. variants: 9
Disease: hearing impairment ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.030 GeneticVariation phenotype BEFREE Mutation of MYH14 can result in a range of neuromuscular phenotypes that includes a dHMN and hearing loss phenotype with variable age of onset.Muscle Nerve 56: 341-345, 2017. 27875632 2017
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.030 Biomarker phenotype BEFREE MYH14 encodes one of the heavy chains of the class II nonmuscle myosins, and it is localized within the autosomal dominant hearing impairment (DFNA4) critical region. 15015131 2004
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.030 GeneticVariation phenotype BEFREE Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation. 11938438 2002