CDH4

cadherin 4
OMIM: 603006, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber CDH4 in Structural eye disease


Version 3.79
Latest signed off version: v3.0 (22 Mar 2023)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Iris coloboma, intellectual disability, and microcephaly