ICD-10: Q71.813

chromosome 17p13.1 deletion syndrome Desbuquois dysplasia fibrochondrogenesis Goldberg-Shprintzen syndrome Schimke immuno-osseous dysplasia Ritscher-Schinzel syndrome Ritscher-Schinzel syndrome 1 Nance-Horan syndrome lethal congenital contracture syndrome 3 lethal congenital contracture syndrome 4 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 3 Miles-Carpenter syndrome monogenic disease campomelic dysplasia Gamstorp-Wohlfart syndrome obsolete SC phocomelia syndrome Charcot-Marie-Tooth disease type X obsolete Saldino-Noonan syndrome brachydactyly acrocapitofemoral dysplasia Allan-Herndon-Dudley syndrome Baller-Gerold syndrome brachyolmia obsolete Opitz-GBBB syndrome proximal symphalangism temtamy preaxial brachydactyly syndrome Perrault syndrome Van Maldergem syndrome Smith-McCort dysplasia acrofacial dysostosis Cincinnati type Galloway-Mowat syndrome 1 Hennekam syndrome orofaciodigital syndrome III acrofacial dysostosis Rodriguez type acrofacial dysostosis, Patagonia type chondrodysplasia Blomstrand type