{"orpha":404568,"name":"Dysostosis of genetic origin","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-404568/","orphanet_url":"https://www.orpha.net/en/disease/detail/404568","names":{"fr":{"name":"Dysostose d'origine génétique"},"de":{"name":"Dysostose, genetisch bedingte"},"es":{"name":"Disostosis de origen genético"},"it":{"name":"Disostosi di origine genetica"},"nl":{"name":"Dysostose van genetische oorsprong"},"pt":{"name":"Disostose genética"},"pl":{"name":"Dyzostoza pochodzenia genetycznego"},"cs":{"name":"Dysostózy genetického původu"},"uk":{"name":"Генетично обумовлений дизостоз"},"zh":{"name":"遗传性骨发育不全"},"tr":{"name":"Genetik kökenli disostoz"}},"xrefs":[{"source":"MONDO","code":"18454","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681144","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":404584,"name":"Rare genetic bone development disorder","classifications":[156]},{"orpha":183524,"name":"Rare genetic bone disease","classifications":[156]}],"children":[{"orpha":66630,"name":"Congenital pseudoarthrosis of the clavicle","type":"Disease"},{"orpha":1531,"name":"Craniosynostosis","type":"Category"},{"orpha":404571,"name":"Dysostosis of genetic origin with limb anomaly as a major feature","type":"Category"},{"orpha":93453,"name":"Dysostosis with predominant craniofacial involvement","type":"Category"},{"orpha":93454,"name":"Dysostosis with predominant vertebral and costal involvement","type":"Category"},{"orpha":93455,"name":"Patellar dysostosis","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}