{"orpha":98657,"name":"OBSOLETE: Genetic vitreous-retinal disease","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 retinal disorder","url":"https://raremap.alftech.space/d/ORPHA-98657/","orphanet_url":"https://www.orpha.net/en/disease/detail/98657","names":{"fr":{"name":"OBSOLETE : Maladie génétique de la rétine et du vitré"},"de":{"name":"OBSOLET: Vitreoretinale Krankheit, genetisch bedingte"},"es":{"name":"OBSOLETO: Enfermedad vitreorretiniana genética"},"it":{"name":"OBSOLETO: Malattia vitreo-retinica"},"nl":{"name":"OBSOLEET: Genetische vitreoretinale ziekte"},"pt":{"name":"OBSOLETO: Doença vítreo-retiniana"},"pl":{"name":"NIEAKTUALNE: Genetyczna choroba witreoretinalna"},"cs":{"name":"NEAKTUÁLNÍ: Geneticky podmíněné vitreoretinální choroby"},"uk":{"name":"ЗАСТАРІЛО: Генетично обумовлене захворювання скловидного тіла та сітківки"},"zh":{"name":"弃用：遗传性玻璃质-视网膜疾病"},"tr":{"name":"Eski adı: Genetik vitreus(vitröz)-retina hastalığı"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":519315,"name":"Rare retinal disorder"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}