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Query OMIM entry list
601687
KRT12
KERATIN 12
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Eye Diseases
Corneal Diseases
Corneal Dystrophies, Hereditary
Eye Diseases, Hereditary
Corneal Dystrophies, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Corneal Dystrophies, Hereditary
Database Center for Life Science
