{"orpha":98694,"name":"OBSOLETE: Spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare brainstem or cerebellar disorder with ophthalmic involvement as a major feature","url":"https://raremap.alftech.space/d/ORPHA-98694/","orphanet_url":"https://www.orpha.net/en/disease/detail/98694","names":{"fr":{"name":"OBSOLETE : Dégénérescence spinocérébelleuse et paraparésie spastique avec anomalie oculomotrice"},"de":{"name":"OBSOLET: Spinozerebelläre Degeneration und spastische Paraparese mit okulomotorischer Anomalie"},"es":{"name":"OBSOLETO: Degeneración espinocerebelosa y paraparesia espástica con anomalía oculomotora"},"it":{"name":"OBSOLETO: Degenerazione spinocerebellare e paraparesi spastica con anomalia oculomotoria"},"nl":{"name":"OBSOLEET: Spinocerebellaire degenerescentie en spastische paraparese met een oculomotorische anomalie"},"pt":{"name":"OBSOLETO: Degenerescência espinocerebelosa e paraparesia espástica com anomalia oculomotora"},"pl":{"name":"NIEAKTUALNE: Zwyrodnienie rdzeniowo-mózdzkowe i parapareza spastyczna z anomalia okoruchowa"},"cs":{"name":"NEAKTUÁLNÍ: Spinocerebelární degenerace a spastické paraparézy s okohybnou anomálií"},"uk":{"name":"ЗАСТАРІЛО: Спіноцеребеллярна дегенерація та спастичний парапарез з окоруховою аномалією"},"zh":{"name":"弃用：脊髓小脑变性和痉挛性截瘫伴眼球运动异常"},"tr":{"name":"Eski adı: Okülomotor anomali ile seyreden spinoserebellar dejeneresan ve spastik paraparezi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":519341,"name":"Rare brainstem or cerebellar disorder with ophthalmic involvement as a major feature"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}