All diseases

OMIM ID
164200
OMIM term:
OCULODENTODIGITAL DYSPLASIA; ODDD
Alternative terms:
ODD SYNDROME
OCULODENTOOSSEOUS DYSPLASIA; ODOD
(∗) Location:
6q22.31  
(†) Associated OMIM genes:
GJA1  
(‡) Associated MGI genes:
Gja1  

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