ICD-10: M89.731

chromosome 18p deletion syndrome chromosome 4q21 deletion syndrome Cole-Carpenter syndrome Desbuquois dysplasia fibrochondrogenesis Schimke immuno-osseous dysplasia lethal congenital contracture syndrome 1 Char syndrome Ritscher-Schinzel syndrome hypertrichotic osteochondrodysplasia Cantu type Ritscher-Schinzel syndrome 2 Yunis-Varon syndrome XFE progeroid syndrome autosomal recessive Robinow syndrome autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 Wilson-Turner syndrome Miles-Carpenter syndrome Leri-Weill dyschondrosteosis obsolete peripheral dysostosis X-linked dominant hypophosphatemic rickets obsolete acroosteolysis Gamstorp-Wohlfart syndrome obsolete SC phocomelia syndrome obsolete Saldino-Noonan syndrome obsolete Majewski syndrome spondylocostal dysostosis brachydactyly ABCD syndrome Askin's tumor anauxetic dysplasia 1 atelosteogenesis Baller-Gerold syndrome Bamforth-Lazarus syndrome Birt-Hogg-Dube syndrome Bjornstad syndrome Boomerang dysplasia Dent disease AGAT deficiency Qazi Markouizos syndrome schneckenbecken dysplasia Ogden syndrome proximal symphalangism Ehlers-Danlos syndrome spondylodysplastic type 2 spondyloepimetaphyseal dysplasia, Pakistani type temtamy preaxial brachydactyly syndrome Marshall-Smith syndrome Koolen de Vries syndrome Townes-Brocks syndrome bone ameloblastoma phalanx chondroma autosomal dominant hypophosphatemic rickets bone benign neoplasm musculoskeletal system benign neoplasm acrofrontofacionasal dysostosis synpolydactyly MASA syndrome Smith-McCort dysplasia Simpson-Golabi-Behmel syndrome type 1 sclerosteosis omodysplasia Ohdo syndrome Ohdo syndrome, SBBYS variant CEDNIK syndrome glucocorticoid-induced osteoporosis acrofacial dysostosis Cincinnati type Galloway-Mowat syndrome 1 orofaciodigital syndrome III orofaciodigital syndrome IV orofaciodigital syndrome VIII orofaciodigital syndrome IX acrofacial dysostosis Rodriguez type acrofacial dysostosis, Catania type