All diseases

OMIM ID
607812
OMIM term:
CRANIOLENTICULOSUTURAL DYSPLASIA; CLSD
Alternative terms:

(∗) Location:
14q21.1  
(†) Associated OMIM genes:
SEC23A  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/suno6eo2