All diseases

OMIM ID
123500
OMIM term:
CROUZON SYNDROME
Alternative terms:
CRANIOFACIAL DYSOSTOSIS, TYPE I; CFD1
CROUZON CRANIOFACIAL DYSOSTOSIS
(∗) Location:
10q26.13  
(†) Associated OMIM genes:
FGFR2  
(‡) Associated MGI genes:
Bey   Fgfr2  

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* quick link - http://q.sanger.ac.uk/wkn30sod