1. Genes and Genomic Entities
  2. CNTN2

CNTN2

contactin 2
OMIM: 190197, Gene2Phenotype

1 panel

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


Level 2: Neurology
Version 8.173
Latest signed off version: v8.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Wessex and West Midlands GLH
    • NHS GMS
    • Radboud University Medical Center, Nijmegen
    Phenotypes
    • Epilepsy, early-onset, 5, with or without developmental delay, OMIM:615400