SE-ATLAS

Primary bone dysplasia with progressive ossification of skin, skeletal muscle, fascia, tendons and ligaments Campomelia, Cumming type Primary intraosseous venous malformation Primary bone dysplasia Osteogenesis imperfecta type 4 Idiopathic phalangeal acro-osteolysis Familial ossifying fibroma Osteochondrosis Adamantinoma Oncogenic osteomalacia Severe lateral tibial bowing-short stature-mild winged scapula-mild facial dysmorphism syndrome Otopalatodigital syndrome spectrum disorder Primary bone dysplasia with micromelia Osteogenesis imperfecta type 5 Maffucci syndrome Epiphysiolysis of the hip Congenital bowing of long bones-short stature-dolichomacrocephaly-ocular hypertelorism syndrome Digestive tract malformation Chondromyxoid fibroma Neural tube defect Diaphragmatic or abdominal wall malformation Dysostosis Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia Spondylometaphyseal dysplasia Osteogenesis imperfecta Dysostosis with limb anomaly as a major feature Rare bone disease Ciliopathies with major skeletal involvement Solitary bone cyst Non-syndromic diaphragmatic or abdominal wall malformation Syndromic diaphragmatic or abdominal wall malformation Multiple metaphyseal dysplasia Multiple epiphyseal dysplasia and pseudoachondroplasia Campomelic dysplasia Syndromic anorectal malformation Spondylodysplastic dysplasia Acromesomelic dysplasia Acromelic dysplasia Campomelic dysplasia and related disorders Mesomelic and rhizo-mesomelic dysplasia Primary bone dysplasia with multiple joint dislocations Non-syndromic anorectal malformation Malformation of the neurenteric canal, spinal cord and column Slender bone dysplasia Gastroduodenal malformation FGFR2-related bent bone dysplasia Chondrodysplasia punctata Congenital vascular bone syndrome Intestinal malformation Primary bone dysplasia with increased bone density Primary bone dysplasia with defective bone mineralization Primary bone dysplasia with decreased bone density Primary osteolysis 22q11.2 deletion syndrome Lysosomal storage disease with skeletal involvement Cleidocranial dysplasia and isolated cranial ossification defect Ollier disease Primary bone dysplasia with disorganized development of skeletal components Dysostosis with predominant vertebral and costal involvement Dysostosis with predominant craniofacial involvement Patellar dysostosis Angioosteohypertrophic syndrome Sagliker syndrome Kyphomelic dysplasia Craniosynostosis Short stature-advanced bone age-early-onset osteoarthritis syndrome Familial osteochondritis dissecans OSLAM syndrome Osteochondritis dissecans Lethal chondrodysplasia Blount disease Bone sarcoma Kosaki overgrowth syndrome Rectal duplication Autosomal dominant polycystic kidney disease Multiple osteochondromas Autosomal recessive polycystic kidney disease Anorectal malformation Parastremmatic dwarfism Non-syndromic diaphragmatic or thoracic malformation Esophageal malformation Osteogenesis imperfecta type 1 Stüve-Wiedemann syndrome Weismann-Netter syndrome Neural tube closure defect Osteonecrosis Inverse Klippel-Trénaunay syndrome Congenital pseudoarthrosis of the clavicle Gorham-Stout disease Osteoblastoma Diaphyseal medullary stenosis-bone malignancy syndrome Osteogenesis imperfecta type 2 Rare bone tumor Angioosteohypotrophic syndrome Osteogenesis imperfecta type 3 Avascular necrosis Large congenital melanocytic nevus Neurocutaneous melanocytosis