{"orpha":183524,"name":"Rare genetic bone disease","type":"Category","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-183524/","orphanet_url":"https://www.orpha.net/en/disease/detail/183524","names":{"fr":{"name":"Maladie osseuse rare d'origine génétique"},"de":{"name":"Knochenkrankheit, genetisch bedingte, seltene"},"es":{"name":"Enfermedades óseas genéticas raras"},"it":{"name":"Malattia genetica rara dell'osso"},"nl":{"name":"Zeldzame genetische botziekte"},"pt":{"name":"Doença óssea genética rara"},"pl":{"name":"Rzadka choroba kości uwarunkowana genetycznie"},"cs":{"name":"Vzácná geneticky podmíněná onemocnění kostí"},"uk":{"name":"Рідкісне генетично обумовлене захворювання кісток"},"zh":{"name":"罕见遗传性骨病"},"tr":{"name":"Nadir genetik kemik hastalığı"}},"xrefs":[{"source":"MONDO","code":"15958","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680561","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93419,"name":"Rare bone disease"},"parents":[{"orpha":98053,"name":"Rare genetic disease","classifications":[156]}],"children":[{"orpha":235832,"name":"Congenital vascular bone syndrome","type":"Clinical group"},{"orpha":404568,"name":"Dysostosis of genetic origin","type":"Category"},{"orpha":93448,"name":"Lysosomal storage disease with skeletal involvement","type":"Category"},{"orpha":399380,"name":"Osteonecrosis of genetic origin","type":"Category"},{"orpha":364526,"name":"Primary bone dysplasia","type":"Category"},{"orpha":364803,"name":"Rare bone disease related to a common gene or pathway defect","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}