All diseases

OMIM ID
119600
OMIM term:
CLEIDOCRANIAL DYSPLASIA; CCD
Alternative terms:
CLEIDOCRANIAL DYSOSTOSIS; CLCD CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED
CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED
(∗) Location:
6p21.1  
(†) Associated OMIM genes:
RUNX2  
(‡) Associated MGI genes:
Ccd   Runx2  

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