{"orpha":183616,"name":"Genetic neuro-ophthalmological disease","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-183616/","orphanet_url":"https://www.orpha.net/en/disease/detail/183616","names":{"fr":{"name":"Maladie neuro-ophtalmologique génétique"},"de":{"name":"Neuro-ophthalmologische Krankheit, genetisch bedingte"},"es":{"name":"Enfermedad neuro-oftalmológica de origen genético"},"it":{"name":"Malattia genetica neuro-oftalmologica"},"nl":{"name":"Genetische neuro-oftalmologische ziekte"},"pt":{"name":"Doença neuro-oftalmológica genética"},"pl":{"name":"Genetyczna choroba neuro-oftalmologiczna"},"cs":{"name":"Geneticky podmíněná neuro-oftalmologická onemocnění"},"uk":{"name":"Генетично обумовлене нейроофтальмологічне захворювання"},"zh":{"name":"遗传性神经-眼疾病"},"tr":{"name":"Genetik nöro-oftalmolojik hastalık"}},"xrefs":[{"source":"UMLS","code":"C5680540","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":522504,"name":"Rare genetic disorder of the visual organs","classifications":[156]}],"children":[{"orpha":522506,"name":"Rare genetic brainstem or cerebellar disorder with ophthalmic involvement as a major feature","type":"Category"},{"orpha":522516,"name":"Rare genetic ocular motility/alignment disorder","type":"Category"},{"orpha":522508,"name":"Rare genetic ophthalmic disorder with cortical involvement","type":"Category"},{"orpha":522510,"name":"Rare genetic ophthalmic disorder with cranial nerve involvement","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}