CNTN2

contactin 2
OMIM: 190197, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red CNTN2 in Early onset or syndromic epilepsy

Level 3: Inherited Epilepsy Syndromes
Level 2: Neurology and neurodevelopmental disorders
Version 5.10
Latest signed off version: v5.0 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood
  • review Not set
    Sources
    • Wessex and West Midlands GLH
    • NHS GMS
    • Radboud University Medical Center, Nijmegen
    Phenotypes
    • Epilepsy, familial adult myoclonic, 5