{"orpha":227786,"name":"OBSOLETE: Familial flecked retinopathy","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Hereditary flecked retinopathy"],"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-227786/","orphanet_url":"https://www.orpha.net/en/disease/detail/227786","names":{"fr":{"name":"OBSOLETE : Rétinopathie en tache familiale","synonyms":["OBSOLETE : Rétinopathie en tache héréditaire"]},"de":{"name":"OBSOLET: Retinopathie, gefleckte, familiäre Form","synonyms":["OBSOLET: Retinopathie, gefleckte, hereditäre"]},"es":{"name":"OBSOLETO: Retinopatía moteada familiar","synonyms":["OBSOLETO: Retinopatía moteada hereditaria"]},"it":{"name":"OBSOLETO: Retinite pigmentosa familiare","synonyms":["OBSOLETO: Retinite pigmentosa ereditaria"]},"nl":{"name":"OBSOLEET: Familiale gespikkelde retinopathie","synonyms":["OBSOLEET: Erfelijke gespikkelde retinopathie"]},"pt":{"name":"OBSOLETO: Retinopatia em listras familiar"},"pl":{"name":"NIEAKTUALNE: Rodzinna retinopatia plamkowata","synonyms":["NIEAKTUALNE: Dziedziczna retinopatia plamkowata"]},"cs":{"name":"NEAKTUÁLNÍ: Familární tečkovaná retinopatie","synonyms":["NEAKTUÁLNÍ: Hereditární tečkovaná retinopatie"]},"uk":{"name":"ЗАСТАРІЛО: Сімейна крапчаста ретинопатія","synonyms":["Спадкова крапчаста ретинопатія: спадкова крапчаста ретинопатія"]},"zh":{"name":"弃用：家族性斑点性视网膜病变","synonyms":["家族性斑点性视网膜病变"]},"tr":{"name":"Eski adı: ailesel benekli retinopati","synonyms":["Kalıtsal benekli retinopati"]}},"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}