{"orpha":85333,"name":"X-linked intellectual disability-spastic paraplegia with iron deposits syndrome","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Arena syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Pelizaeus-Merzbacher disease","url":"https://raremap.alftech.space/d/ORPHA-85333/","orphanet_url":"https://www.orpha.net/en/disease/detail/85333","names":{"fr":{"name":"Syndrome de déficience intellectuelle liée à l'X-paraplégie spastique avec dépots de fer","synonyms":["Syndrome d'Arena"]},"de":{"name":"X-chromosomale Intelligenzminderung-spastische Paraplegie mit Eisenablagerung-Syndrom","synonyms":["Arena-Syndrom"]},"es":{"name":"Síndrome de discapacidad intelectual-paraplejía espástica con acúmulo de hierro ligado al cromosoma X","synonyms":["Síndrome de Arena"]},"it":{"name":"Sindrome disabilità cognitiva legata all'X-paraplegia spastica con depositi di ferro","synonyms":["Sindrome di Arena"]},"nl":{"name":"X-gebonden intellectuele achterstand - spastische paraplegie met ijzerdepositie-syndroom","synonyms":["Syndroom van Arena"]},"pt":{"name":"Perturbação do desenvolvimento intelectual-paraplegia espástica com depósitos de ferro ligada ao X","synonyms":["Síndrome Arena"]},"pl":{"name":"Niepełnosprawność intelektualna sprzężona z chromosomem X - spastyczna paraplegia z odkładaniem żelaza","synonyms":["Zespół Arena"]},"cs":{"name":"Syndrom zahrnující X-vázanou mentální retardaci a spastickou paraplegii s depozity železa","synonyms":["Arenův syndrom"]},"uk":{"name":"Синдром Х-зчепленої розумової відсталостї-спастичної параплегії з відкладеннями заліза","synonyms":["Синдром Арени"]},"zh":{"name":"X连锁智力障碍-痉挛性截瘫铁伴铁沉积综合征","synonyms":["Arena综合征"]},"tr":{"name":"X'e bağlı zihinsel yetersizlik-spastik parapleji ile seyreden demir birikintileri sendromu","synonyms":["Arena sendromu"]}},"xrefs":[{"source":"UMLS","code":"C2931491","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":702,"name":"Pelizaeus-Merzbacher disease"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}