ICD-10: M89.561

Simpson-Golabi-Behmel syndrome type 1 omodysplasia Rapp-Hodgkin syndrome Stormorken syndrome Vici syndrome Galloway-Mowat syndrome 1 chondrodysplasia Blomstrand type chromosome 6q24-q25 deletion syndrome Cole-Carpenter syndrome Warsaw breakage syndrome Barber-Say syndrome Yunis-Varon syndrome XFE progeroid syndrome chondrodysplasia-pseudohermaphroditism syndrome lethal congenital contracture syndrome 4 autosomal recessive Robinow syndrome Leri-Weill dyschondrosteosis mesocestoidiasis obsolete peripheral dysostosis hypophosphatemia mulibrey nanism Gamstorp-Wohlfart syndrome Charcot-Marie-Tooth disease type 1 Charcot-Marie-Tooth disease type 3 obsolete Majewski syndrome anauxetic dysplasia 1 atelosteogenesis Baller-Gerold syndrome Bamforth-Lazarus syndrome Boomerang dysplasia Ogden syndrome Ehlers-Danlos syndrome spondylodysplastic type 2 fibroma Townes-Brocks syndrome bone benign neoplasm osteoblastoma Warburg micro syndrome MASA syndrome Smith-McCort dysplasia