All diseases

OMIM ID
125400
OMIM term:
DENTIN DYSPLASIA, TYPE I; DTDP1
Alternative terms:
DENTIN DYSPLASIA, SHIELDS TYPE I
ROOTLESS TEETH
RADICULAR DENTIN DYSPLASIA DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH, INCLUDED
(∗) Location:
6q27  
(†) Associated OMIM genes:
SMOC2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/peok718g