{"orpha":522546,"name":"Rare genetic disorder with lens opacification","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-522546/","orphanet_url":"https://www.orpha.net/en/disease/detail/522546","names":{"fr":{"name":"Maladie génétique rare d'opacification du cristallin"},"de":{"name":"Seltene genetische Krankheit mit Opakifikation der Linse"},"es":{"name":"Trastorno genético raro con opacificación de la lente"},"it":{"name":"Malattia genetica rara con opacizzazione della lente"},"nl":{"name":"Zeldzame genetische stoornis met lensopacificatie","synonyms":["Zeldzame genetische stoornis met vertroebeling van de ooglens"]},"pt":{"name":"Doença genética rara com opacificação do cristalino"},"pl":{"name":"Rzadka choroba uwarunkowana genetycznie ze zmętnieniem soczewek"},"cs":{"name":"Vzácná genetická porucha s opacitou čočky"},"uk":{"name":"Рідкісне генетично обумовлене захворювання з помутнінням кришталика"},"zh":{"name":"罕见遗传性疾病伴有晶状体混浊"},"tr":{"name":"Lens opasifikasyonu ile seyreden nadir genetik bozukluk"}},"xrefs":[{"source":"UMLS","code":"C5681419","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":183607,"name":"Genetic lens and zonula anomaly","classifications":[156]}],"children":[{"orpha":91492,"name":"Early onset non-syndromic cataract","type":"Disease"},{"orpha":522548,"name":"Syndromic genetic cataract","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}