{"orpha":716367,"name":"Rare isolated non-progressive generalized retinal disorder","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"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-716367/","orphanet_url":"https://www.orpha.net/en/disease/detail/716367","names":{"fr":{"name":"Maladie rare isolée rétinienne non-progressive généralisée"},"de":{"name":"Seltene isolierte nicht-progrediente generalisierte Retinopathie"},"es":{"name":"Trastorno retiniano generalizado no progresivo aislado raro"},"it":{"name":"Retinopatia generalizzata rara isolata non progressiva"},"nl":{"name":"Zeldzame geïsoleerde niet-progressieve gegeneraliseerde aandoening van retina"},"pt":{"name":"Rare isolated non-progressive generalized retinal disorder"},"pl":{"name":"Rzadkie izolowane niepostępujące uogólnione zaburzenie siatkówki"},"cs":{"name":"Rare isolated non-progressive generalized retinal disorder"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":716364,"name":"Rare non-progressive generalized retinal disorder","classifications":[156,189]}],"children":[{"orpha":49382,"name":"Achromatopsia","type":"Disease"},{"orpha":16,"name":"Blue cone monochromatism","type":"Disease"},{"orpha":75374,"name":"Bradyopsia","type":"Disease"},{"orpha":215,"name":"Congenital stationary night blindness","type":"Clinical group"},{"orpha":363989,"name":"Familial benign flecked retina","type":"Disease"},{"orpha":99179,"name":"Kandori fleck retina","type":"Malformation syndrome"},{"orpha":75378,"name":"Oligocone trichromacy","type":"Disease"},{"orpha":714041,"name":"Straatsma syndrome","type":"Disease"},{"orpha":90001,"name":"X-linked cone dysfunction syndrome with myopia","type":"Disease"},{"orpha":792,"name":"X-linked retinoschisis","type":"Malformation syndrome"},{"orpha":178333,"name":"Åland Islands eye disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}