MYL1

myosin light chain 1
OMIM: 160780
PanelMode of inheritanceDetails
2 panels
R-numbers: R83
Signed-off version 3.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
congenital myopathy
Component of the following Super Panels:
  • - Hypotonic infant
  • - Neuromuscular disorders
R-numbers: R81
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
congenital myopathy, Myopathy, congenital, with fast-twitch (type II) fiber atrophy, 618414