ICD-10: M89.541

monogenic disease obsolete peripheral dysostosis Carney complex Charcot-Marie-Tooth disease type 4 Charcot-Marie-Tooth disease type X obsolete Saldino-Noonan syndrome obsolete Majewski syndrome cranioectodermal dysplasia brachydactyly Askin's tumor anauxetic dysplasia 1 atelosteogenesis Baller-Gerold syndrome Bart-Pumphrey syndrome Bjornstad syndrome Boomerang dysplasia brachydactyly-syndactyly syndrome brachyolmia Brody myopathy Ogden syndrome tarsal-carpal coalition syndrome Ehlers-Danlos syndrome spondylodysplastic type 2 Perrault syndrome Marshall-Smith syndrome autosomal dominant hypophosphatemic rickets janus kinase-3 deficiency autoimmune disease of musculoskeletal system obsolete skeletal system benign neoplasm Kennedy's disease Warburg micro syndrome Van Maldergem syndrome Smith-McCort dysplasia sclerosteosis omodysplasia CEDNIK syndrome Native American myopathy hypoparathyroidism-retardation-dysmorphism syndrome Galloway-Mowat syndrome 1 Hennekam syndrome orofaciodigital syndrome IV orofaciodigital syndrome VII orofaciodigital syndrome IX chondrodysplasia Blomstrand type chromosome 19q13.11 deletion syndrome Cole-Carpenter syndrome MEDNIK syndrome EAST syndrome Schimke immuno-osseous dysplasia Char syndrome Ritscher-Schinzel syndrome 3MC syndrome 3 Yunis-Varon syndrome Nance-Horan syndrome Muenke Syndrome autosomal recessive Robinow syndrome autosomal dominant Robinow syndrome 1 Miles-Carpenter syndrome osteoporosis-pseudoglioma syndrome Potocki-Lupski syndrome