{"orpha":140653,"name":"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-140653/","orphanet_url":"https://www.orpha.net/en/disease/detail/140653","names":{"fr":{"name":"Maladie neuro-ophtalmologique"},"de":{"name":"Neuro-ophthalmologische Krankheit"},"es":{"name":"Enfermedad neuro-oftalmológica"},"it":{"name":"Malattia neuro-oftalmica"},"nl":{"name":"Neuro-oftalmologische ziekte"},"pt":{"name":"Doença neuro-oftalmológica"},"pl":{"name":"Choroba neurooftalmologiczna"},"cs":{"name":"Neuro-oftalmologická onemocnění"},"uk":{"name":"Нейроофтальмологічні захворювання"},"zh":{"name":"神经-眼病"},"tr":{"name":"Nöro-oftalmolojik hastalık"}},"xrefs":[{"source":"MONDO","code":"15368","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680678","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19930","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":98691,"name":"OBSOLETE: Abnormal eye movements","status":"inactive"},{"type":"Referred to","orpha":98692,"name":"OBSOLETE: Nervous system anomaly with eye involvement","status":"inactive"}],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":520814,"name":"Rare disorder of the visual organs","classifications":[189]}],"children":[{"orpha":519341,"name":"Rare brainstem or cerebellar disorder with ophthalmic involvement as a major feature","type":"Category"},{"orpha":519355,"name":"Rare ocular motility/alignment disorder","type":"Category"},{"orpha":519343,"name":"Rare ophthalmic disorder with cortical involvement","type":"Category"},{"orpha":519349,"name":"Rare ophthalmic disorder with cranial nerve involvement","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}