CNTN4

contactin 4
OMIM: 607280, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red CNTN4 in Autism


Level 2: Neurology and neurodevelopmental disorders
Version 0.198

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Intellectual disability
  • SCA

Red CNTN4 in Mendeliome


Version 1.1891

review Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
  • Victorian Clinical Genetics Services

Red CNTN4 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • Intellectual disability
  • SCA