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GENATLAS PHENOTYPE

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

Remark(s)