All diseases

OMIM ID
123100
OMIM term:
CRANIOSYNOSTOSIS, TYPE 1; CRS1
Alternative terms:
CRANIOSYNOSTOSIS; CRS
CRANIOSTENOSIS SCAPHOCEPHALY, INCLUDED
OXYCEPHALY, INCLUDED
(∗) Location:
7p21.1  
(†) Associated OMIM genes:
TWIST1  
(‡) Associated MGI genes:
Axin2  

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