MEG3

maternally expressed 3 (non-protein coding)
OMIM: 605636, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red MEG3 in Paediatric motor neuronopathies


Level 2: Neurology
Version 3.12
Latest signed off version: v3.9 (30 Apr 2025)

Component of the following Super Panels:

  • Hypotonic infant
  • Other rare neuromuscular disorders
  • review Not set
    Sources
    • Expert Review Red
    Tags
    • locus-type-rna-long-non-coding