{"orpha":717324,"name":"Rare genetic isolated progressive generalized retinal disorder","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Non-syndromic inherited retinal dystrophy","Non-syndromic IRD"],"definition":null,"note":"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.","url":"https://raremap.alftech.space/d/ORPHA-717324/","orphanet_url":"https://www.orpha.net/en/disease/detail/717324","names":{"fr":{"name":"Maladie génétique rare isolée rétinienne progressive généralisée","synonyms":["Dystrophie héréditaire de la rétine non syndromique"]},"de":{"name":"Seltene genetische isolierte progrediente generalisierte Retinopathie","synonyms":["Nicht-syndromale hereditäre Netzhautdystrophie"]},"es":{"name":"Trastorno retiniano generalizado progresivo aislado genético raro","synonyms":["Distrofia retiniana hereditaria no sindrómica","DRH no sindrómica"]},"it":{"name":"Retinopatia genetica rara progressiva generalizzata isolata","synonyms":["IRD non sindromica","Distrofia retinica ereditaria non sindromica"]},"nl":{"name":"Zeldzame genetische geïsoleerde progressieve gegeneraliseerde aandoening van retina","synonyms":["Niet-syndromale erfelijke retinadystrofie","Niet-syndromale IRD","Zeldzame genetische geïsoleerde progressieve gegeneraliseerde aandoening van netvlies"]},"pt":{"name":"Rare genetic isolated progressive generalized retinal disorder"},"pl":{"name":"Rzadkie genetycznie uwarunkowane postępujące uogólnione zaburzenie dotyczące siatkówki","synonyms":["Non-syndromic inherited retinal dystrophy","Non-syndromic IRD"]},"cs":{"name":"Rare genetic isolated progressive generalized retinal disorder","synonyms":["Non-syndromic inherited retinal dystrophy","Non-syndromic IRD"]}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":717321,"name":"Rare genetic progressive generalized retinal disorder","classifications":[156]},{"orpha":716410,"name":"Rare isolated progressive generalized retinal disorder","classifications":[189]}],"children":[{"orpha":139455,"name":"Autosomal recessive bestrophinopathy","type":"Disease"},{"orpha":85128,"name":"Bothnia retinal dystrophy","type":"Disease"},{"orpha":209932,"name":"Cone dystrophy with supernormal rod response","type":"Disease"},{"orpha":1872,"name":"Cone rod dystrophy","type":"Disease"},{"orpha":53540,"name":"Goldmann-Favre syndrome","type":"Disease"},{"orpha":67042,"name":"Late-onset retinal degeneration","type":"Disease"},{"orpha":65,"name":"Leber congenital amaurosis","type":"Disease"},{"orpha":247834,"name":"Occult macular dystrophy","type":"Disease"},{"orpha":1871,"name":"Progressive cone dystrophy","type":"Disease"},{"orpha":352718,"name":"Progressive retinal dystrophy due to retinol transport defect","type":"Disease"},{"orpha":397758,"name":"Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies","type":"Disease"},{"orpha":791,"name":"Retinitis pigmentosa","type":"Disease"},{"orpha":52427,"name":"Retinitis punctata albescens","type":"Disease"},{"orpha":364055,"name":"Severe early-childhood-onset retinal dystrophy","type":"Disease"},{"orpha":827,"name":"Stargardt disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}