1. Genes and Genomic Entities
  2. MYMX

MYMX

myomixer, myoblast fusion factor
Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green MYMX in Congenital myopathy


Level 2: Neurology
Version 7.81
Latest signed off version: v7.77 (12 Aug 2026)

Component of the following Super Panels:

  • Hypotonic infant
  • Other rare neuromuscular disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    • Literature
    Phenotypes
    • Carey-Fineman-Ziter syndrome 2, OMIM:619941
    • Carey-Fineman-Ziter syndrome 2, MONDO:0100292
    Amber MYMX in Fetal anomalies


    Level 2: Fetal (including NIPD)
    Version 8.26
    Latest signed off version: v8.0 (12 Aug 2026)

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Amber
    Phenotypes
    • Carey-Fineman-Ziter syndrome 2
    • OMIM:619941