Home Page
References OMIM Gene GeneReviews HGMD HGNC
last update : 26-02-2009
Symbol KRTT
Location 11p13
Name keratitis hereditary
Corresponding gene PAX6
Main clinical features
  • childhood corneal clotting, characterized by recurrent stromal keratitis and vascularization
  • variation in the severity of the corneal changes, with generally more progressive keratitis among older affected persons
  • Genetic determination autosomal dominant
    Function/system disorder eye
    Type disease