{"orpha":717330,"name":"Rare genetic isolated non-progressive predominantly macular 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-717330/","orphanet_url":"https://www.orpha.net/en/disease/detail/717330","names":{"fr":{"name":"Maladie génétique rare isolée avec atteinte non-progressive prédominante de la macula"},"de":{"name":"Seltene genetische isolierte nicht-progrediente Makulopathie"},"es":{"name":"Trastorno genético raro predominantemente macular no progresivo aislado"},"it":{"name":"Malattia genetica rara non progressiva a predominanza maculare isolata"},"nl":{"name":"Zeldzame genetische geïsoleerde niet-progressieve aandoening van voornamelijk macula","synonyms":["Zeldzame genetische geïsoleerde niet-progressieve aandoening van voornamelijk gele vlek","Zeldzame genetische geïsoleerde niet-progressieve overwegend maculaire aandoening"]},"pt":{"name":"Rare genetic isolated non-progressive predominantly macular disorder"},"pl":{"name":"Rzadkie genetycznie uwarunkowane izolowane niepostępujące zaburzenie dotyczące głównie plamki"},"cs":{"name":"Rare genetic isolated non-progressive predominantly macular disorder"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":717327,"name":"Rare genetic non-progressive predominantly macular disorder","classifications":[156]}],"children":[{"orpha":98945,"name":"Coloboma of macula","type":"Morphological anomaly"},{"orpha":519398,"name":"Isolated foveal hypoplasia","type":"Morphological anomaly"},{"orpha":75327,"name":"North Carolina macular dystrophy","type":"Disease"},{"orpha":178333,"name":"Åland Islands eye disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}