All diseases

OMIM ID
612913
OMIM term:
OROFACIODIGITAL SYNDROME XI; OFD11
Alternative terms:
OFDS XI
ORAL-FACIAL-DIGITAL SYNDROME, TYPE XI
ORAL-FACIAL-DIGITAL SYNDROME WITH SKELETAL ANOMALIES
GABRIELLI SYNDROME
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/nrwy3ke9