- OMIM ID
-
143095
- OMIM term:
- SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS
- Alternative terms:
-
HUMEROSPINAL DYSOSTOSIS; HSD
SPONDYLOEPIPHYSEAL DYSPLASIA, OMANI TYPE
CHONDRODYSPLASIA WITH MULTIPLE DISLOCATIONS; CDMD
- (∗) Location:
- 10q22.1
- (†) Associated OMIM genes:
- CHST3
- (‡) Associated MGI genes:
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