Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79784
Gene Symbol: MYH14
MYH14
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.320 Biomarker CLINGEN Interestingly, all reported cases to date of MYH14-related nonsyndromic hearing loss with detailed phenotypes have demonstrated mild-to-moderate progressive hearing loss with postlingual onset. 28221712

2017

Entrez Id: 79784
Gene Symbol: MYH14
MYH14
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.320 Biomarker CLINGEN Loss of Myh14 Increases Susceptibility to Noise-Induced Hearing Loss in CBA/CaJ Mice. 28101381

2016

Entrez Id: 79784
Gene Symbol: MYH14
MYH14
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.320 Biomarker CLINGEN Genetic association of MYH genes with hereditary hearing loss in Korea. 27393652

2016

Entrez Id: 79784
Gene Symbol: MYH14
MYH14
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.320 Biomarker CLINGEN Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric population. 25719458

2015

Entrez Id: 79784
Gene Symbol: MYH14
MYH14
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.320 Biomarker CLINGEN Whole-exome sequencing to decipher the genetic heterogeneity of hearing loss in a Chinese family with deaf by deaf mating. 25289672

2014

Entrez Id: 79784
Gene Symbol: MYH14
MYH14
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.320 Biomarker CLINGEN Candidate gene association study for noise-induced hearing loss in two independent noise-exposed populations. 19183343

2009

Entrez Id: 79784
Gene Symbol: MYH14
MYH14
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.320 Biomarker CLINGEN Genetic heterogeneity of deafness phenotypes linked to DFNA4. 16222661

2005

Entrez Id: 79784
Gene Symbol: MYH14
MYH14
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.320 Biomarker CLINGEN Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4). 15015131

2004