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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
  • coronal craniosynostosis, very heterogeneous, with or without associated malformation
  • Genetic determination autosomal dominant
    Related entries DEL7P21, TWIST, ACS1
    Function/system disorder congenital malformation
    Type malformation
    Remark(s)