All diseases

OMIM ID
271665
OMIM term:
SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE
Alternative terms:
SMED-SL
SMED, SHORT LIMB-HAND TYPE
SMED, TYPE II
SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-ABNORMAL CALCIFICATION TYPE
SMED, SHORT LIMB-ABNORMAL CALCIFICATION TYPE
SMED-SL/AC
(∗) Location:
1q23.3  
(†) Associated OMIM genes:
DDR2  
(‡) Associated MGI genes:

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