{"orpha":101435,"name":"Rare genetic eye disease","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Rare genetic ophthalmologic disease"],"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-101435/","orphanet_url":"https://www.orpha.net/en/disease/detail/101435","names":{"fr":{"name":"Maladie génétique rare de l'oeil","synonyms":["Maladie génétique rare des yeux","Maladie ophtalmologique génétique rare"]},"de":{"name":"Augenkrankheit, genetisch bedingte"},"es":{"name":"Enfermedades oculares genéticas raras"},"it":{"name":"Malattia oculare genetica"},"nl":{"name":"Zeldzame genetische oogziekte","synonyms":["Genetische oftalmologische ziekte"]},"pt":{"name":"Doença ocular, genética"},"pl":{"name":"Rzadkie genetyczne choroby oczu","synonyms":["Genetyczna choroba oftalmologiczna"]},"cs":{"name":"Vzácná geneticky podmíněná onemocnění oka","synonyms":["Vzácné genetické oftalmologické onemocnění"]},"uk":{"name":"Рідкісне генетично обумовлене захворювання очей","synonyms":["Рідкісне генетичне офтальмологічне захворювання"]},"zh":{"name":"罕见遗传性眼病","synonyms":["罕见遗传性眼科疾病"]},"tr":{"name":"Nadir genetik göz hastalığı","synonyms":["Nadir genetik oftalmolojik hastalık"]}},"xrefs":[{"source":"MONDO","code":"15107","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680375","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19782","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":98053,"name":"Rare genetic disease","classifications":[156]}],"children":[{"orpha":98658,"name":"Color-vision disease","type":"Category"},{"orpha":183619,"name":"Genetic eye tumor","type":"Category"},{"orpha":522504,"name":"Rare genetic disorder of the visual organs","type":"Category"},{"orpha":98618,"name":"Rare refraction anomaly","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}