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GENATLAS PHENOTYPE |
last update : 16-05-2018 |
Symbol | FECD9 |
Location | 18q21.1 |
Name | corneal dystrophy, Fuchs endothelial 9 |
Corresponding gene | LOXHD1 |
Main clinical features |
|
Genetic determination | autosomal dominant |
Function/system disorder | eye |
Type | disease |
Remark(s) |