{"orpha":1852,"name":"OBSOLETE: X-linked retinal dysplasia","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Norrie disease","url":"https://raremap.alftech.space/d/ORPHA-1852/","orphanet_url":"https://www.orpha.net/en/disease/detail/1852","names":{"fr":{"name":"OBSOLETE : Dysplasie rétinienne liée à l'X"},"de":{"name":"OBSOLET: Retinadysplasie, X-chromosomale"},"es":{"name":"OBSOLETO: Displasia retiniana ligada al cromosoma X"},"it":{"name":"OBSOLETO: Displasia retinica legata all'X"},"nl":{"name":"OBSOLEET: X-gebonden retinale dysplasie","synonyms":["NIET ZELDZAME ZIEKTE IN EUROPA: X-gebonden retinadysplasie","NIET ZELDZAME ZIEKTE IN EUROPA: X-gebonden dysplasie van netvlies"]},"pt":{"name":"OBSOLETO: Displasia da retina ligada ao X","synonyms":["OBSOLETO: Retinopatia ligada ao X"]},"pl":{"name":"NIEAKTUALNE: Dysplazja siatkówki sprzężona z chromosomem X"},"cs":{"name":"NEAKTUÁLNÍ: X-vázaná retinální dysplázie"},"uk":{"name":"Х-зчеплена дисплазія сітківки","definition":"A rare genetic eye disease characterized by abnormal proliferation of retinal tissue resulting in the formation of retinal folds, thereby causing gliosis and, clinically, variable degrees of visual impairment. No clinical findings other than those associated with the eyes have been demonstrated."},"zh":{"name":"X连锁视网膜发育不良"},"tr":{"name":"X'e bağlı retina displazisi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":649,"name":"Norrie disease"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}