{"orpha":98618,"name":"Rare refraction anomaly","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-98618/","orphanet_url":"https://www.orpha.net/en/disease/detail/98618","names":{"fr":{"name":"Anomalie rare de la réfraction"},"de":{"name":"Refraktionsstörung, seltene"},"es":{"name":"Anomalía rara de la refracción"},"it":{"name":"Anomalia rara della rifrazione"},"nl":{"name":"Zeldzame refractieanomalie"},"pt":{"name":"Anomalia refrativa, rara"},"pl":{"name":"Rzadka wada refrakcji"},"cs":{"name":"Vzácné refrakční anomálie"},"uk":{"name":"Рідкісна аномалія рефракції"},"zh":{"name":"罕见折光异常"},"tr":{"name":"Nadir kırma kusuru anomalisi"}},"xrefs":[{"source":"UMLS","code":"C5681677","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":98620,"name":"OBSOLETE: Syndromic myopia","status":"inactive"},{"type":"Referred to","orpha":183601,"name":"OBSOLETE: Rare genetic refraction anomaly","status":"inactive"}],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":101435,"name":"Rare genetic eye disease","classifications":[156]},{"orpha":97966,"name":"Rare ophthalmic disorder","classifications":[189]}],"children":[{"orpha":98621,"name":"Rare hyperopia and astigmatism","type":"Category"},{"orpha":98619,"name":"Rare isolated myopia","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}