ICD-10: M89.73

Hirata disease monogenic disease obsolete peripheral dysostosis mulibrey nanism campomelic dysplasia obsolete acroosteolysis obsolete SC phocomelia syndrome congenital disorder of glycosylation type I ABCD syndrome Askin's tumor anauxetic dysplasia 1 atelosteogenesis Baller-Gerold syndrome Bart-Pumphrey syndrome Boomerang dysplasia brachydactyly-syndactyly syndrome schneckenbecken dysplasia Meckel syndrome CHARGE syndrome Perrault syndrome Townes-Brocks syndrome bone benign neoplasm osteoblastoma acrofrontofacionasal dysostosis Adams-Oliver syndrome Smith-McCort dysplasia sclerosteosis omodysplasia CEDNIK syndrome hypoparathyroidism-retardation-dysmorphism syndrome acrofacial dysostosis Cincinnati type Stormorken syndrome Galloway-Mowat syndrome 1 Hennekam syndrome Cole-Carpenter syndrome Desbuquois dysplasia fibrochondrogenesis MEDNIK syndrome EAST syndrome Char syndrome Ritscher-Schinzel syndrome Holzgreve-Wagner-Rehder Syndrome Ritscher-Schinzel syndrome 1 Ritscher-Schinzel syndrome 2 Yunis-Varon syndrome Nance-Horan syndrome ulnar-mammary syndrome autosomal recessive Robinow syndrome autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 3 Miles-Carpenter syndrome Leri-Weill dyschondrosteosis osteoporosis-pseudoglioma syndrome orofaciodigital syndrome XI orofaciodigital syndrome IX acrofacial dysostosis Rodriguez type acrofacial dysostosis, Catania type chondrodysplasia Blomstrand type chromosomal deletion syndrome