All diseases

OMIM ID
304110
OMIM term:
CRANIOFRONTONASAL SYNDROME; CFNS
Alternative terms:
CRANIOFRONTONASAL DYSPLASIA; CFND
CRANIOFRONTONASAL DYSOSTOSIS
(∗) Location:
Xq13.1  
(†) Associated OMIM genes:
EFNB1  
(‡) Associated MGI genes:
Efnb1  

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* quick link - http://q.sanger.ac.uk/cshh6rx8