All diseases

OMIM ID
175700
OMIM term:
GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; GCPS
Alternative terms:

(∗) Location:
7p14.1  
(†) Associated OMIM genes:
GLI3  
(‡) Associated MGI genes:
Gli3  

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* quick link - http://q.sanger.ac.uk/mtm27xjz