{"orpha":519298,"name":"Rare scleral disorder","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-519298/","orphanet_url":"https://www.orpha.net/en/disease/detail/519298","names":{"fr":{"name":"Maladie rare de la sclérotique"},"de":{"name":"Seltene Krankheit der Sklera"},"es":{"name":"Trastorno raro de la esclerótica"},"it":{"name":"Patologia sclerale rara"},"nl":{"name":"Zeldzame aandoening van sclera"},"pt":{"name":"Doença rara da esclera"},"pl":{"name":"Rzadka choroba twardówki"},"cs":{"name":"Vzácná porucha skléry"},"uk":{"name":"Рідкісний склеральний розлад"},"zh":{"name":"罕见的巩膜病变"},"tr":{"name":"Nadir skleral bozukluk"}},"xrefs":[{"source":"UMLS","code":"C5681369","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":520814,"name":"Rare disorder of the visual organs","classifications":[189]}],"children":[{"orpha":519296,"name":"Rare disorder with pigmented sclera","type":"Category"},{"orpha":648559,"name":"Rare scleritis","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}