All diseases

OMIM ID
304120
OMIM term:
OTOPALATODIGITAL SYNDROME, TYPE II; OPD2
Alternative terms:
OPD II SYNDROME
OPD SYNDROME 2
CRANIOORODIGITAL SYNDROME
FACIOPALATOOSSEOUS SYNDROME; FPO
(∗) Location:
Xq28  
(†) Associated OMIM genes:
FLNA  
(‡) Associated MGI genes:
Flna  

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