ICD-10: Q79.8

Meier-Gorlin syndrome acrofacial dysostosis, Catania type chondrodysplasia Blomstrand type chromosome 3q29 microdeletion syndrome chromosome 17q21.31 duplication syndrome MEDNIK syndrome Schimke immuno-osseous dysplasia Barber-Say syndrome lethal congenital contracture syndrome 2 Ritscher-Schinzel syndrome 1 lethal congenital contracture syndrome 3 lethal congenital contracture syndrome 4 EEC syndrome Wilson-Turner syndrome obsolete Brooks-Wisniewski-Brown syndrome Poland syndrome obsolete physical disorder OBSOLETED TERM Farber lipogranulomatosis Loeys-Dietz syndrome Gamstorp-Wohlfart syndrome obsolete SC phocomelia syndrome acrocapitofemoral dysplasia Allan-Herndon-Dudley syndrome Bamforth-Lazarus syndrome dyskinetic cerebral palsy Brooke-Spiegler syndrome funisitis PSPH deficiency Qazi Markouizos syndrome proximal symphalangism multiple synostoses syndrome cone dystrophy spondyloepiphyseal dysplasia with congenital joint dislocations acrofrontofacionasal dysostosis omodysplasia oculodentodigital dysplasia