CNTN3

contactin 3
OMIM: 601325, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red CNTN3 in Mendeliome


Version 1.2374

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, CNTN3-related

Red CNTN3 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.83

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, CNTN3-related