OVOL2:Ensemblv90

ovo like zinc finger 2
OMIM: 616441, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green OVOL2 in Corneal Dystrophy


Level 2: Ophthalmological disorders
Version 1.13

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Corneal dystrophy, posterior polymorphous, 1, MIM# 122000
Tags
  • 5'UTR

Green OVOL2 in Mendeliome


Version 1.3802

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Corneal dystrophy, posterior polymorphous, 1, MIM# 122000
Tags
  • 5'UTR

Green OVOL2 in Corneal Dystrophy


Level 2: Ophthalmological disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green
Phenotypes
  • Corneal dystrophy, posterior polymorphous, 1, MIM# 122000
Tags
  • 5'UTR