- OMIM ID
-
184250
- OMIM term:
- SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK
- Alternative terms:
-
SEMD, STRUDWICK TYPE
SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE
SMED, STRUDWICK TYPE
SMED, TYPE I
STRUDWICK SYNDROME
DAPPLED METAPHYSIS SYNDROME
SPONDYLOMETAPHYSEAL DYSPLASIA; SMD
SEMDC
- (∗) Location:
- 12q13.11
- (†) Associated OMIM genes:
- COL2A1
- (‡) Associated MGI genes:
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