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GENATLAS PHENOTYPE

last update : 11-02-2014

Symbol	KTCN9
Location	20p13
Name	keratoconus 9
Corresponding gene	SLC4A11
Main clinical features	thinning and anterior protrusion of the cornea that results in altered refractive powers and loss of visual acuity
Genetic determination	autosomal dominant
Function/system disorder	eye
Type	disease

Remark(s)