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) |