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GENATLAS PHENOTYPE |
last update : 26-10-2018 |
Symbol | CCA3 |
Location | 2q33.3 |
Name | cataract, congenital, cerulean type 3 |
Other name(s) |
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Corresponding gene | CRYGD |
Other symbol(s) | . CTRCT4 |
Main clinical features | moroccan family with early onset and fasting progression |
Genetic determination | autosomal dominant |
Function/system disorder | eye |
Type | disease |
Gene product |
Name | gamma D crystallin |
Remark(s) |