MYH14

myosin heavy chain 14
OMIM: 608568
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Nonsyndromic Hearing Loss, Dominant, Deafness, autosomal dominant 4A, 600652, ?Peripheral neuropathy, myopathy, hoarseness, and hearing loss, 614369