Home Page |
References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 26-10-2018 |
Symbol | CATM2 |
Location | 22q12 |
Name | cataract with associated microphthalmia 2 |
Other name(s) |
|
Corresponding gene | CRYBA4 |
Other symbol(s) | CTRCT23 |
Main clinical features | microphthalmia, microcornea, and congenital cataract |
Genetic determination | autosomal dominant |
Function/system disorder | eye |
Type | disease |
Remark(s) |