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 6.1
Latest signed off version: v6.0 (6 May 2026)

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