{"orpha":98646,"name":"Renal disease with cataract","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-98646/","orphanet_url":"https://www.orpha.net/en/disease/detail/98646","names":{"fr":{"name":"Maladie rénale avec cataracte"},"de":{"name":"Katarakt mit assoziierter Nierenkrankheit"},"es":{"name":"Enfermedad renal con una posible catarata"},"it":{"name":"Cataratta associata a malattia renale"},"nl":{"name":"Renale ziekte met cataract"},"pt":{"name":"Doença renal com catarata"},"pl":{"name":"Choroba nerek z zaćmą"},"cs":{"name":"Onemocnění ledvin s kataraktou"},"uk":{"name":"Захворювання нирок з катарактою"},"zh":{"name":"肾脏疾病伴白内障"},"tr":{"name":"Katarakt ile seyreden böbrek hastalığı"}},"xrefs":[{"source":"UMLS","code":"C5681666","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":98641,"name":"Syndromic cataract","classifications":[189]},{"orpha":522548,"name":"Syndromic genetic cataract","classifications":[156]}],"children":[{"orpha":63,"name":"Alport syndrome","type":"Disease"},{"orpha":534,"name":"Oculocerebrorenal syndrome of Lowe","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}