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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 22/06/2006 |
Symbol | CRS |
Location | 7p21.1 |
HGNC id | 2369 |
Name | craniosynostosis, syndromatic 1 |
Other name(s) | craniosynostosis |
Corresponding gene | TWIST1 |
Other symbol(s) | CRS1, CRSR, CSOCRS, CSO |
Main clinical features |
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Genetic determination | autosomal dominant |
Related entries | DEL7P21, TWIST, ACS1 |
Function/system disorder | congenital malformation |
Type | malformation |
Remark(s) |