{"orpha":519315,"name":"Rare retinal 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-519315/","orphanet_url":"https://www.orpha.net/en/disease/detail/519315","names":{"fr":{"name":"Maladie rétinienne rare"},"de":{"name":"Seltene Krankheit der Retina"},"es":{"name":"Trastorno retiniano raro"},"it":{"name":"Patologia retinica rara"},"nl":{"name":"Zeldzame aandoening van retina","synonyms":["Zeldzame aandoening van netvlies"]},"pt":{"name":"Doença retiniana rara"},"pl":{"name":"Rzadka choroba siatkówki"},"cs":{"name":"Vzácná porucha sítnice"},"uk":{"name":"Рідкісне захворювання сітківки"},"zh":{"name":"罕见视网膜病变"},"tr":{"name":"Nadir retina bozukluğu"}},"xrefs":[{"source":"UMLS","code":"C5681377","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":98657,"name":"OBSOLETE: Genetic vitreous-retinal disease","status":"inactive"},{"type":"Referred to","orpha":98661,"name":"OBSOLETE: Syndromic rod-cone dystrophy","status":"inactive"}],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":519311,"name":"Rare disorder of the posterior segment of the eye","classifications":[189]}],"children":[{"orpha":716358,"name":"Rare generalized retinal disorder","type":"Category"},{"orpha":519313,"name":"Rare macular disorder","type":"Category"},{"orpha":716290,"name":"Rare predominantly chorioretinal disorder","type":"Category"},{"orpha":519317,"name":"Rare retinal vasculopathy","type":"Category"},{"orpha":98668,"name":"Vitreoretinopathy","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}