All diseases

OMIM ID
218330
OMIM term:
CRANIOECTODERMAL DYSPLASIA 1; CED1
Alternative terms:
SENSENBRENNER SYNDROME
LEVIN SYNDROME I
(∗) Location:
3q21.3-q22.1  
(†) Associated OMIM genes:
IFT122  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/dh22ybfk