ICD-10: M89.732

osteoporosis-pseudoglioma syndrome Carpenter syndrome MASA syndrome Smith-McCort dysplasia Simpson-Golabi-Behmel syndrome type 1 omodysplasia oculodentodigital dysplasia Meier-Gorlin syndrome CEDNIK syndrome Galloway-Mowat syndrome 1 Hennekam syndrome orofaciodigital syndrome III orofaciodigital syndrome VII orofaciodigital syndrome VIII orofaciodigital syndrome IX acrofacial dysostosis, Catania type chondrodysplasia Blomstrand type Cole-Carpenter syndrome fibrochondrogenesis MEDNIK syndrome Barber-Say syndrome lethal congenital contracture syndrome 2 Char syndrome Holzgreve-Wagner-Rehder Syndrome Ritscher-Schinzel syndrome 1 Ritscher-Schinzel syndrome 2 Yunis-Varon syndrome Nance-Horan syndrome ulnar-mammary syndrome Muenke Syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 3 Miles-Carpenter syndrome Leri-Weill dyschondrosteosis obsolete peripheral dysostosis mulibrey nanism campomelic dysplasia obsolete acroosteolysis Gamstorp-Wohlfart syndrome obsolete SC phocomelia syndrome obsolete Saldino-Noonan syndrome obsolete Majewski syndrome spondylocostal dysostosis cranioectodermal dysplasia anauxetic dysplasia 1 Baller-Gerold syndrome Bjornstad syndrome Boomerang dysplasia Bowen-Conradi syndrome brachydactyly-syndactyly syndrome brachyolmia Dent disease schneckenbecken dysplasia proximal symphalangism fibular hypoplasia and complex brachydactyly Ehlers-Danlos syndrome spondylodysplastic type 2 spondyloepimetaphyseal dysplasia, Pakistani type temtamy preaxial brachydactyly syndrome Marshall-Smith syndrome Koolen de Vries syndrome bone ameloblastoma hereditary hypophosphatemic rickets with hypercalciuria bone benign neoplasm osteoblastoma acrofrontofacionasal dysostosis Adams-Oliver syndrome Baraitser-Winter syndrome