MYH14, myosin heavy chain 14, 79784

N. diseases: 64; N. variants: 9
Disease: Peripheral Neuropathy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy 		0.020 GeneticVariation group BEFREE The R941L mutation in MYH14 disrupts mitochondrial fission and associates with peripheral neuropathy. 31231018 2019
CUI: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy 		0.020 GeneticVariation group 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