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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 28/08/2006 |
Symbol | OPD1 |
Location | Xq28 |
Name | otopalatodigital syndrome, type 1 |
Other name(s) | OPD syndrome, type 1 |
Corresponding gene | FLNA |
Main clinical features |
|
Genetic determination | sex linked |
Function/system disorder | osteo-articular |
congenital malformation | |
Type | disease |
Gene product |
Name | filamin A |
Remark(s) |