All diseases

OMIM ID
257920
OMIM term:
3MC SYNDROME 1; 3MC1
Alternative terms:
OCULOPALATOSKELETAL SYNDROME
CRANIOSYNOSTOSIS WITH LID ANOMALIES
MICHELS SYNDROME, FORMERLY
(∗) Location:
3q27.3  
(†) Associated OMIM genes:
MASP1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/ee51vag9