{"orpha":63454,"name":"Pattern dystrophy","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Patterned dystrophy of the retinal pigment epithelium"],"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-63454/","orphanet_url":"https://www.orpha.net/en/disease/detail/63454","names":{"fr":{"name":"Pattern dystrophie","synonyms":["Dystrophie tachetée du pôle postérieur"]},"de":{"name":"Musterdystrophien des retinalen Pigmentepithels"},"es":{"name":"Displasia en patrón del epitelio pigmentario de la retina"},"it":{"name":"Distrofia dell'epitelio pigmentato della retina"},"nl":{"name":"Patroondystrofie","synonyms":["Patroondystrofie van retinaal pigmentepitheel"]},"pt":{"name":"Distrofia em padrão","synonyms":["Distrofia em padrão do epitélio pigmentar da retina"]},"pl":{"name":"Dystrofie wzorzyste nabłonka barwnikowego siatkówki","synonyms":["Patterned dystrophy of the retinal pigment epithelium"]},"cs":{"name":"Pigmentová pattern dystrofie","synonyms":["Pattern dystrofie retinálního pigmentového epitelu"]},"uk":{"name":"Патерноподібна дистрофія","synonyms":["Патернальна дистрофія пігментного епітелію сітківки"]},"zh":{"name":"视网膜色素上皮图形状营养不良","synonyms":["图案状视网膜色素上皮萎缩"]},"tr":{"name":"Pattern distrofisi","synonyms":["Retina pigment epitelinin paternli distrofisi"]}},"xrefs":[{"source":"MONDO","code":"18973","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"C536309","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1868569","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"9821","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":717336,"name":"Rare genetic isolated progressive predominantly macular disorder","classifications":[156]},{"orpha":716432,"name":"Rare isolated progressive predominantly macular disorder","classifications":[189]}],"children":[{"orpha":99000,"name":"Adult-onset foveomacular vitelliform dystrophy","type":"Disease"},{"orpha":99001,"name":"Butterfly-shaped pigment dystrophy","type":"Disease"},{"orpha":99004,"name":"Fundus pulverulentus","type":"Disease"},{"orpha":99003,"name":"Multifocal pattern dystrophy simulating fundus flavimaculatus","type":"Disease"},{"orpha":99002,"name":"Reticular dystrophy of the retinal pigment epithelium","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":["Autosomal dominant","Autosomal recessive"],"onset":["Adult"],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Not yet validated","source":"ORPHANET"}],"phenotypes":null}