CDH11

cadherin 11
OMIM: 600023, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red CDH11 in Autism


Version 0.22

review Not set
Sources
  • Expert Review Red
  • SFARI

Green CDH11 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 3.1677
Latest signed off version: v3.2 (13 Feb 2020)

Component of the following Super Panels:

  • Hypotonic infant
  • Paediatric disorders
  • White matter disorders - childhood onset
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    • Expert Review Green
    • Expert Review Green
    • Literature
    Phenotypes
    • Elsahy-Waters syndrome, OMIM:211380
    • Teebi hypertelorism syndrome

    Green CDH11 in Severe Paediatric Disorders


    Version 1.127

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Next Generation Children Project
    • Expert Review Green
    • Expert list
    Phenotypes
    • Elsahy-Waters syndrome, 211380