All diseases

OMIM ID
183900
OMIM term:
SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA; SEDC
Alternative terms:
SED CONGENITA
SPONDYLOEPIPHYSEAL DYSPLASIA, CONGENITAL TYPE
(∗) Location:
12q13.11  
(†) Associated OMIM genes:
COL2A1  
(‡) Associated MGI genes:
Col2a1   Hapln1  

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