{"orpha":93419,"name":"Rare bone disease","type":"Category","group":"Group of disorders","status":"active","flags":["Head of classification"],"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-93419/","orphanet_url":"https://www.orpha.net/en/disease/detail/93419","names":{"fr":{"name":"Maladie osseuse rare"},"de":{"name":"Knochenkrankheit, seltene"},"es":{"name":"Enfermedad ósea rara"},"it":{"name":"Malattia ossea rara"},"nl":{"name":"Zeldzame botziekte"},"pt":{"name":"Doença óssea, rara"},"pl":{"name":"Rzadkie choroby kości"},"cs":{"name":"Vzácná onemocnění kostí"},"uk":{"name":"Рідкісне захворювання кісток"},"zh":{"name":"罕见骨病"},"tr":{"name":"Nadir kemik hastalığı"}},"xrefs":[{"source":"UMLS","code":"C5681602","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[{"orpha":235832,"name":"Congenital vascular bone syndrome","type":"Clinical group"},{"orpha":364559,"name":"Dysostosis","type":"Category"},{"orpha":168621,"name":"Dysplasia of head of femur, Meyer type","type":"Disease"},{"orpha":647823,"name":"Idiopathic pregnancy-associated osteoporosis","type":"Disease"},{"orpha":93448,"name":"Lysosomal storage disease with skeletal involvement","type":"Category"},{"orpha":352540,"name":"Oncogenic osteomalacia","type":"Disease"},{"orpha":399158,"name":"Osteonecrosis","type":"Category"},{"orpha":364526,"name":"Primary bone dysplasia","type":"Category"},{"orpha":68411,"name":"Rare bone tumor","type":"Category"},{"orpha":300493,"name":"Sagliker syndrome","type":"Particular clinical situation in a disease or syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}