MB

myoglobin
OMIM: 160000, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red MB in Congenital myopathy


Level 2: Neurology
Version 6.45
Latest signed off version: v6.0 (30 Apr 2025)

Component of the following Super Panels:

  • Hypotonic infant
  • Other rare neuromuscular disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Other
    Phenotypes
    • Myopathy, sarcoplasmic body, OMIM:620286