Home Page
References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 14-03-2012
Symbol MYP21
Location 1p22.2
Name myopia 21
Corresponding gene ZNF644
Main clinical features refractive error of less than 6 diopters, combined with astigmatism, impaired vision, and moderate hypoplasia of the optic nerve heads
Genetic determination autosomal dominant
Function/system disorder eye
Type disease
Remark(s)