{"orpha":717336,"name":"Rare genetic isolated 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-717336/","orphanet_url":"https://www.orpha.net/en/disease/detail/717336","names":{"fr":{"name":"Maladie génétique rare isolée avec atteinte progressive prédominante de la macula"},"de":{"name":"Seltene genetische isolierte progrediente Makulopathie"},"es":{"name":"Trastorno genético raro predominantemente macular progresivo aislado"},"it":{"name":"Malattia genetica rara progressiva a predominanza maculare isolata"},"nl":{"name":"Zeldzame genetische geïsoleerde progressieve aandoening van voornamelijk macula","synonyms":["Zeldzame genetische geïsoleerde progressieve aandoening van voornamelijk gele vlek","Zeldzame genetische geïsoleerde progressieve overwegend maculaire aandoening"]},"pt":{"name":"Rare genetic isolated progressive predominantly macular disorder"},"pl":{"name":"Rzadkie genetycznie uwarunkowane izolowane postępujące zaburzenie dotyczące głównie plamki"},"cs":{"name":"Rare genetic isolated progressive predominantly macular disorder"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":717333,"name":"Rare genetic progressive predominantly macular disorder","classifications":[156]}],"children":[{"orpha":75376,"name":"Autosomal dominant drusen","type":"Disease"},{"orpha":139455,"name":"Autosomal recessive bestrophinopathy","type":"Disease"},{"orpha":1243,"name":"Best vitelliform macular dystrophy","type":"Disease"},{"orpha":41751,"name":"Bietti crystalline dystrophy","type":"Disease"},{"orpha":75377,"name":"Central areolar choroidal dystrophy","type":"Disease"},{"orpha":75381,"name":"Cystoid macular dystrophy","type":"Disease"},{"orpha":67042,"name":"Late-onset retinal degeneration","type":"Disease"},{"orpha":263347,"name":"MRCS syndrome","type":"Disease"},{"orpha":466718,"name":"Martinique crinkled retinal pigment epitheliopathy","type":"Disease"},{"orpha":247834,"name":"Occult macular dystrophy","type":"Disease"},{"orpha":63454,"name":"Pattern dystrophy","type":"Category"},{"orpha":319640,"name":"Retinal macular dystrophy type 2","type":"Disease"},{"orpha":59181,"name":"Sorsby fundus dystrophy","type":"Disease"},{"orpha":827,"name":"Stargardt disease","type":"Disease"},{"orpha":792,"name":"X-linked retinoschisis","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}