{"orpha":716432,"name":"Rare 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-716432/","orphanet_url":"https://www.orpha.net/en/disease/detail/716432","names":{"fr":{"name":"Maladie rare isolée avec atteinte progressive prédominante de la macula"},"de":{"name":"Seltene isolierte progrediente Makulopathie"},"es":{"name":"Trastorno raro predominantemente macular progresivo aislado"},"it":{"name":"Malattia rara isolata progressiva a predominanza maculare"},"nl":{"name":"Zeldzame geïsoleerde progressieve overwegend maculaire aandoening","synonyms":["Zeldzame geïsoleerde progressieve aandoening van voornamelijk macula","Zeldzame geïsoleerde progressieve aandoening van voornamelijk gele vlek"]},"pt":{"name":"Rare iolated progressive predominantly macular disorder"},"pl":{"name":"Rzadkie postępujące zaburzenie dotyczące głównie plamki"},"cs":{"name":"Rare isolated progressive predominantly macular disorder"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":716416,"name":"Rare progressive predominantly macular disorder","classifications":[189]}],"children":[{"orpha":284460,"name":"Acute annular outer retinopathy","type":"Disease"},{"orpha":715855,"name":"Acute exudative polymorphous vitelliform maculopathy","type":"Disease"},{"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":440727,"name":"Combined hamartoma of the retina and retinal pigment epithelium","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":2737,"name":"Onchocerciasis","type":"Disease"},{"orpha":63454,"name":"Pattern dystrophy","type":"Category"},{"orpha":97341,"name":"Persistent placoid maculopathy","type":"Disease"},{"orpha":482092,"name":"Rare idiopathic macular telangiectasia","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":714150,"name":"Stellate non-hereditary idiopathic foveomacular retinoschisis","type":"Disease"},{"orpha":279894,"name":"Toxic maculopathy due to antimalarial drugs","type":"Disease"},{"orpha":792,"name":"X-linked retinoschisis","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}