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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 05-07-2017 |
Symbol | EVR7 |
Location | 3p22.1 |
Name | familial exudative vitreoretinopathy 7 |
Corresponding gene | CTNNB1 |
Main clinical features |
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Genetic determination | autosomal dominant |
Function/system disorder | eye |
Type | disease |
Remark(s) |