{"orpha":93443,"name":"Neonatal osteosclerotic dysplasia","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-93443/","orphanet_url":"https://www.orpha.net/en/disease/detail/93443","names":{"fr":{"name":"Ostéosclérose néonatale"},"de":{"name":"Dysplasie, neonatale osteosklerotische"},"es":{"name":"Displasia osteosclerótica neonatal"},"it":{"name":"Displasia osteosclerotica neonatale"},"nl":{"name":"Neonatale osteosclerotische dysplasie"},"pt":{"name":"Displasia osteosclerótica neonatal"},"pl":{"name":"Dysplazja osteosklerotyczna noworodków"},"cs":{"name":"Novorozenecké osteosklerotické dysplázie"},"uk":{"name":"Неонатальна остеосклеротична дисплазія"},"zh":{"name":"新生儿骨硬化性发育不良"},"tr":{"name":"Yenidoğan osteosklerotik displazi"}},"xrefs":[{"source":"MONDO","code":"0019702","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1300205","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93419,"name":"Rare bone disease"},"parents":[{"orpha":93444,"name":"Primary bone dysplasia with increased bone density","classifications":[147,156,199]}],"children":[{"orpha":50945,"name":"Blomstrand lethal chondrodysplasia","type":"Malformation syndrome"},{"orpha":1310,"name":"Caffey disease","type":"Malformation syndrome"},{"orpha":35107,"name":"Desmosterolosis","type":"Disease"},{"orpha":1832,"name":"Osteosclerotic bone dysplasia","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}