Home Page

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)