All diseases

OMIM ID
271550
OMIM term:
SPONDYLOENCHONDRODYSPLASIA; SPENCD
Alternative terms:
SPONDYLOMETAPHYSEAL DYSPLASIA WITH ENCHONDROMATOUS CHANGES
SPONDYLOENCHONDROMATOSIS; SEM SPONDYLOENCHONDRODYSPLASIA WITH D-2-HYDROXYGLUTARIC ACIDURIA, INCLUDED
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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