1. Genes and Genomic Entities
  2. CDH11

CDH11

cadherin 11
OMIM: 600023, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Amber CDH11 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.181
Latest signed off version: v6.0 (30 Apr 2025)

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
Phenotypes
  • Teebi hypertelorism syndrome 2, OMIM:619736
  • Elsahy-Waters syndrome
Green CDH11 in DDG2P


Version 6.447
Latest signed off version: v6.0 (30 Apr 2025)

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


    Level 2: Developmental disorders
    Version 9.345
    Latest signed off version: v9.0 (30 Apr 2025)

    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