Specific

Albright's hereditary osteodystrophy (AHO) atelosteogenesis type II (neonatal osseous dysplasia I) autosomal dominant syndactyly; nonsyndromic syndactyly Caffey's disease (infantile cortical hyperostosis) cleidocranial dysplasia cranioosteoarthropathy Crouzon syndrome (craniofacial dysostosis type 1, Crouzon craniofacial dysostosis) diastrophic dysplasia dyssegmental dysplasia Silverman-Handmaker type (DDSH) Ellis-van Creveld syndrome (chondroectodermal dysplasia) Grieg cephalopolysyndactyly syndrome hereditary rickets hypophosphatemic nephrolithiasis/osteoporosis type 1 inherited disorder of osteolysis; vanishing bone syndrome; osteolysis syndrome Jackson-Weiss syndrome Jansen-type metaphyseal chondrodysplasia juvenile Paget's disease; hyperostosis corticalis deformans juvenilis; hereditary hyperphosphatasia; chronic congenital idiopathic hyperphosphatasia nail-patella syndrome (onychoosteodysplasia) osteogenesis imperfecta; osteopsathyrosis; fragilitas ossium; Lobstein's disease (OI) osteopathia striata with cranial sclerosis osteoporosis pseudoglioma syndrome; osteogenesis imperfecta ocular form postaxial acrofacial dysostosis (Miller syndrome) primary hypertrophic osteoarthropathy (pachydermoperiostosis) progressive pseudorheumatoid arthropathy of childhood skeletal dysplasia Upington disease Weyers acrofacial dysostosis (Curry-Hall syndrome) X-linked hypophosphatemia

General

bone disease; osteopathia chronic musculoskeletal disease genetic disease