SYT15

synaptotagmin 15
OMIM: 608081, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red SYT15 in Congenital myaesthenic syndrome


Level 2: Neurology
Version 5.7
Latest signed off version: v5.0 (30 Apr 2025)

Component of the following Super Panels:

  • Hypotonic infant
  • Other rare neuromuscular disorders
  • review Not set
    Sources
    • Expert Review Red
    • NHS GMS
    • Wessex and West Midlands GLH