ICD-10: M89

autosomal dominant Robinow syndrome 1 Miles-Carpenter syndrome Ehlers-Danlos syndrome spondylodysplastic type 2 ameloblastoma hereditary hypophosphatemic rickets with hypercalciuria autosomal dominant hypophosphatemic rickets acrofrontofacionasal dysostosis Van Maldergem syndrome obsolete peripheral dysostosis Gamstorp-Wohlfart syndrome acrocapitofemoral dysplasia Boomerang dysplasia Smith-McCort dysplasia sclerosteosis Ohdo syndrome, SBBYS variant Meier-Gorlin syndrome hypoparathyroidism-retardation-dysmorphism syndrome acrofacial dysostosis Rodriguez type chondrodysplasia Blomstrand type Cole-Carpenter syndrome Schimke immuno-osseous dysplasia autosomal dominant Robinow syndrome 2