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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 22/06/2006 |
Symbol | CVT |
Location | 2q31.1 |
Name | congenital vertical talus |
Other name(s) |
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Corresponding gene | HOXD10 |
Main clinical features |
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Genetic determination | autosomal dominant |
Function/system disorder | osteo-articular |
Type | disease |
Gene product |
Name | homeo box D10 |
Remark(s) |