CNTN3

contactin 3
OMIM: 601325, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red CNTN3 in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI
Red CNTN3 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.13
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Victorian Clinical Genetics Services
    • Literature