All diseases

OMIM ID
311300
OMIM term:
OTOPALATODIGITAL SYNDROME, TYPE I; OPD1
Alternative terms:
OPD I SYNDROME
OPD SYNDROME 1 OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED
FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED
(∗) Location:
Xq28  
(†) Associated OMIM genes:
FLNA  
(‡) Associated MGI genes:
Flna  

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