{"orpha":665,"name":"Albright hereditary osteodystrophy","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Pseudohypoparathyroidism","url":"https://raremap.alftech.space/d/ORPHA-665/","orphanet_url":"https://www.orpha.net/en/disease/detail/665","names":{"fr":{"name":"Ostéodystrophie héréditaire d'Albright"},"de":{"name":"Albright-Osteodystrophie, hereditäre","synonyms":["Osteodystrophie, hereditäre Albright'sche"]},"es":{"name":"Osteodistrofia hereditaria de Albright"},"it":{"name":"Osteodistrofia ereditaria di Albright"},"nl":{"name":"Albright erfelijke osteodystrofie"},"pt":{"name":"Osteodistrofia hereditária de Albright"},"pl":{"name":"Dziedziczna osteodystrofia Albrighta"},"cs":{"name":"Albrightova hereditární osteodystrofie"},"uk":{"name":"Спадкова остеодистрофія Олбрайта"},"zh":{"name":"Albright遗传性骨营养不良症"},"tr":{"name":"Albright kalıtsal osteodistrofisi"}},"xrefs":[{"source":"UMLS","code":"C2931404","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":97593,"name":"Pseudohypoparathyroidism"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}