- OMIM ID
-
166750
- OMIM term:
- OTODENTAL DYSPLASIA
- Alternative terms:
-
CHROMOSOME 11q13 DELETION SYNDROME
OTODENTAL SYNDROME OTODENTAL SYNDROME WITH COLOBOMA, INCLUDED
OCULOOTODENTAL SYNDROME, INCLUDED
- (∗) Location:
- 11q13
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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