CDH11

cadherin 11
OMIM: 600023, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green CDH11 in Mendeliome


Version 1.1891

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Elsahy-Waters syndrome, MIM# 211380
  • Teebi hypertelorism syndrome

Green CDH11 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genetic Health Queensland
Phenotypes
  • Elsahy-Waters syndrome, MIM# 211380
  • Teebi hypertelorism syndrome

Green CDH11 in Mackenzie's Mission_Reproductive Carrier Screening


Level 2: Screening
Version 0.109

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Elsahy-Waters syndrome, 211380 (3), Autosomal recessive

Green CDH11 in Prepair 1000+


Level 2: Screening
Version 1.9

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Elsahy-Waters syndrome, 211380 (3), Autosomal recessive