All diseases

OMIM ID
311200
OMIM term:
OROFACIODIGITAL SYNDROME I; OFD1
Alternative terms:
ORAL-FACIAL-DIGITAL SYNDROME, TYPE I
OFDS I
PAPILLON-LEAGE AND PSAUME SYNDROME
(∗) Location:
Xp22.2  
(†) Associated OMIM genes:
OFD1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/x5yh3iga