SYT15

synaptotagmin 15
OMIM: 608081, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Red SYT15 in Congenital myaesthenic syndrome Level 3: Neuromuscular disorders Level 2: Neurology and neurodevelopmental disorders Version 4.6 Latest signed off version: v4.5 (1 May 2024) 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

Panel

Reviews

Mode of inheritance

Details

Red SYT15 in Congenital myaesthenic syndrome

Level 3: Neuromuscular disorders
Level 2: Neurology and neurodevelopmental disorders
Version 4.6
Latest signed off version: v4.5 (1 May 2024)

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