{"orpha":519325,"name":"OBSOLETE: Syndromic inherited retinal disorder","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Syndromic retinal dystrophy"],"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 genetic retinal disorder","url":"https://raremap.alftech.space/d/ORPHA-519325/","orphanet_url":"https://www.orpha.net/en/disease/detail/519325","names":{"fr":{"name":"OBSOLETE : Maladie rétinienne héréditaire syndromique"},"de":{"name":"OBSOLET: Syndromale hereditäre retinale Störung","synonyms":["OBSOLET: Netzhautdystrophie, syndromale","OBSOLET: Syndromale Netzhautdystrophie"]},"es":{"name":"OBSOLETO: Trastorno retiniano hereditario sindrómico","synonyms":["OBSOLETO: Distrofia retiniana sindrómica"]},"it":{"name":"OBSOLETO: Patologia retinica sindromica ereditaria","synonyms":["OBSOLETO: Distrofia retinica sindromica"]},"nl":{"name":"OBSOLEET: Syndromale erfelijke aandoening van retina","synonyms":["NIET ZELDZAME ZIEKTE IN EUROPA: Syndromale retinale dystrofie","NIET ZELDZAME ZIEKTE IN EUROPA: Syndromale erfelijke aandoening van netvlies"]},"pt":{"name":"OBSOLETO: Doença retiniana hereditária sindromática"},"pl":{"name":"NIEAKTUALNE: Dziedziczna syndromiczna choroba siatkówki","synonyms":["NIEAKTUALNE: Zespół dystrofii siatkówki"]},"cs":{"name":"NEAKTUÁLNÍ: Syndromická dědičná porucha sítnice","synonyms":["NEAKTUÁLNÍ: Syndromická dystrofie sítnice"]},"uk":{"name":"Синдромне спадкове захворювання сітківки","synonyms":["Синдромальна дистрофія сітківки"]},"zh":{"name":"综合征性遗传性视网膜病变","synonyms":["综合性视网膜营养不良"]},"tr":{"name":"Sendromik kalıtsal retina bozukluğu","synonyms":["Sendromik retina distrofisi"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":522572,"name":"Rare genetic retinal disorder"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}