MYH1

myosin heavy chain 1
OMIM: 160730, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red MYH1 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • rhabdomyolysis, MONDO:0005290

Red MYH1 in Rhabdomyolysis and Metabolic Myopathy


Level 2: Neurology and neurodevelopmental disorders
Version 1.6

Component of the following Super Panels:

  • Myopathy Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    • Literature
    Phenotypes
    • rhabdomyolysis, MONDO:0005290