ICD-10: M89.76

autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 3 Leri-Weill dyschondrosteosis osteoporosis-pseudoglioma syndrome chondrodysplasia Blomstrand type Desbuquois dysplasia fibrochondrogenesis MEDNIK syndrome Schimke immuno-osseous dysplasia Barber-Say syndrome lethal congenital contracture syndrome 2 Holzgreve-Wagner-Rehder Syndrome Ritscher-Schinzel syndrome 2 3MC syndrome 1 Yunis-Varon syndrome Nance-Horan syndrome lethal congenital contracture syndrome 4 autosomal recessive Robinow syndrome autosomal dominant Robinow syndrome 2 obsolete Actinomadura madurae infectious disease obsolete peripheral dysostosis campomelic dysplasia Gamstorp-Wohlfart syndrome obsolete SC phocomelia syndrome obsolete Majewski syndrome brachydactyly acrocapitofemoral dysplasia anauxetic dysplasia 1 atelosteogenesis Baller-Gerold syndrome Bart-Pumphrey syndrome Bowen-Conradi syndrome brachyolmia PSAT deficiency Qazi Markouizos syndrome schneckenbecken dysplasia Meckel syndrome Kahrizi syndrome spondyloepiphyseal dysplasia with congenital joint dislocations Perrault syndrome Marshall-Smith syndrome bone ameloblastoma janus kinase-3 deficiency Adams-Oliver syndrome Smith-McCort dysplasia Simpson-Golabi-Behmel syndrome type 1 omodysplasia Rapp-Hodgkin syndrome CEDNIK syndrome orofaciodigital syndrome III orofaciodigital syndrome VIII acrofacial dysostosis Rodriguez type