All diseases

OMIM ID
106600
OMIM term:
TOOTH AGENESIS, SELECTIVE, 1; STHAG1
Alternative terms:
HYPODONTIA/OLIGODONTIA 1; HYD1
SECOND PREMOLARS AND THIRD MOLARS, ABSENCE OF
TOOTH AGENESIS, FAMILIAL TOOTH AGENESIS, SELECTIVE, WITH OROFACIAL CLEFT, INCLUDED
HYPODONTIA/OLIGODONTIA WITH OROFACIAL CLEFT, INCLUDED
(∗) Location:
4p16.2  
(†) Associated OMIM genes:
MSX1  
(‡) Associated MGI genes:
Msx1   Pax9  

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