1. Genes and Genomic Entities
  2. CDH11

CDH11

cadherin 11
OMIM: 600023, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Red CDH11 in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI
Green CDH11 in DDG2P


Version 3.87
Latest signed off version: v3.1 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • CDH11-related, OMIM:211380
    Green CDH11 in Intellectual disability - microarray and sequencing

    Level 3: Neurodevelopmental disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 5.532
    Latest signed off version: v5.0 (22 Mar 2023)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  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 1.184

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