All diseases

OMIM ID
165590
OMIM term:
OROFACIODIGITAL SYNDROME X; OFD10
Alternative terms:
OFDS X
ORAL-FACIAL-DIGITAL SYNDROME, TYPE X
OROFACIODIGITAL SYNDROME WITH FIBULAR APLASIA
ORAL-FACIAL-DIGITAL SYNDROME WITH FIBULAR APLASIA
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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