MYH2

myosin heavy chain 2
OMIM: 160740
PanelMode of inheritanceDetails
2 panels
Component of the following Super Panels:
  • - Hypotonic infant
  • - Neuromuscular disorders
R-numbers: R81
Signed-off version 3.1
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Proximal myopathy and ophthalmoplegia, OMIM:605637, Myopathy, proximal, and ophthalmoplegia, MONDO:0011577
R-numbers: R21, R412
Signed-off version 2.4
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Proximal myopathy and ophthalmoplegia, OMIM:605637, Myopathy, proximal, and ophthalmoplegia, MONDO:0011577