Spondyloepiphyseal dysplasia, Nishimura type (Orphanet_163649, an Orphanet rare-disease nomenclature term) can be described as follows. Spondyloepiphyseal dysplasia Nishimura type is characterized by spondyloepiphyseal dysplasia, craniosynostosis, cataracts, cleft palate and intellectual deficit. Also known as: Spondyloepiphyseal dysplasia - craniosynostosis - cleft palate - cataract - intellectual disability.