All diseases

OMIM ID
272460
OMIM term:
SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT
Alternative terms:
SPONDYLOCARPOTARSAL SYNDROME
SYNSPONDYLISM, CONGENITAL
VERTEBRAL FUSION WITH CARPAL COALITION
SCOLIOSIS, CONGENITAL, WITH UNILATERAL UNSEGMENTED BAR
(∗) Location:
3p14.3  
(†) Associated OMIM genes:
FLNB  
(‡) Associated MGI genes:
Flnb  

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