{"orpha":183601,"name":"OBSOLETE: Rare genetic refraction anomaly","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare refraction anomaly","url":"https://raremap.alftech.space/d/ORPHA-183601/","orphanet_url":"https://www.orpha.net/en/disease/detail/183601","names":{"fr":{"name":"OBSOLETE : Anomalie génétique rare de la réfraction"},"de":{"name":"OBSOLET: Refraktionsanomalie, genetisch bedingte, seltene"},"es":{"name":"OBSOLETO: Anomalía genética rara de refracción"},"it":{"name":"OBSOLETO: Anomalia genetica rara della rifrazione"},"nl":{"name":"OBSOLEET: Zeldzame genetische refractieanomalie"},"pt":{"name":"OBSOLETO: Anomalia de refração genética rara"},"pl":{"name":"NIEAKTUALNE: Rzadka genetyczna wada refrakcji"},"cs":{"name":"NEAKTUÁLNÍ: Vzácné dědičné refrakční anomálie"},"uk":{"name":"ЗАСТАРІЛО: Рідкісна генетично обумовлена аномалія рефракції"},"zh":{"name":"弃用：罕见遗传性折射异常"},"tr":{"name":"Eski adı: Nadir genetik kırılma anomalisi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":98618,"name":"Rare refraction anomaly"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}