KRT3

keratin 3
OMIM: 148043, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green KRT3 in Corneal Dystrophy


Level 2: Ophthalmological disorders
Version 1.20

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Meesmann corneal dystrophy 2, MIM# 618767

Green KRT3 in Mendeliome


Version 1.4220

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Meesmann corneal dystrophy 2, MIM# 618767