MYH14, myosin heavy chain 14, 79784

N. diseases: 64; N. variants: 9
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0019825
Disease: Hoarseness
Hoarseness
0.110 Biomarker phenotype BEFREE Although mutations in MYH14 have been shown to cause nonsyndromic autosomal dominant hearing loss (DFNA4), the peripheral neuropathy, myopathy, and hoarseness have not been associated with MYH14. 21480433 2011
CUI: C0019825
Disease: Hoarseness
Hoarseness
0.110 Biomarker phenotype HPO