{"orpha":98666,"name":"OBSOLETE: Unclassified primitive or secondary maculopathy","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 genetic retinal disorder","url":"https://raremap.alftech.space/d/ORPHA-98666/","orphanet_url":"https://www.orpha.net/en/disease/detail/98666","names":{"fr":{"name":"OBSOLETE : Maculopathie primaire ou secondaire non classifiée"},"de":{"name":"OBSOLET: Makulopathie, primäre oder sekundäre, sonstige"},"es":{"name":"OBSOLETO: Maculopatía primaria o secundaria no clasificada"},"it":{"name":"OBSOLETO: Maculopatia primaria o secondaria non classificata"},"nl":{"name":"OBSOLEET: Niet-geclassificeerde primitieve of secundaire maculopathie"},"pt":{"name":"OBSOLETO: Maculopatia primária ou secundária, outras"},"pl":{"name":"NIEAKTUALNE: Niesklasyfikowana makulopatia pierwotna lub wtórna"},"cs":{"name":"NEAKTUÁLNÍ: Neklasifikované primitivní nebo sekundární makulopatie"},"uk":{"name":"ЗАСТАРІЛО: некласифікована первинна або вторинна макулопатія"},"zh":{"name":"弃用：未分类原发性或继发性黄斑病变"},"tr":{"name":"Eski adı: Sınıflandırılmamış primitif veya sekonder makülopati"}},"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}