CNTN6

contactin 6
OMIM: 607220, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red CNTN6 in Mendeliome


Version 1.2302

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, CNTN6-related
Tags
  • disputed

Red CNTN6 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.63

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, CNTN6-related
Tags
  • disputed