All diseases

OMIM ID
218600
OMIM term:
BALLER-GEROLD SYNDROME; BGS
Alternative terms:
CRANIOSYNOSTOSIS WITH RADIAL DEFECTS
CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME
(∗) Location:
8q24.3  
(†) Associated OMIM genes:
RECQL4  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/fhf5skb7