All diseases

OMIM ID
122860
OMIM term:
CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD
Alternative terms:

(∗) Location:
17q21.31  
(†) Associated OMIM genes:
SOST  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/0tgi67ya