{"orpha":522572,"name":"Rare genetic 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-522572/","orphanet_url":"https://www.orpha.net/en/disease/detail/522572","names":{"fr":{"name":"Maladie génétique rétinienne rare"},"de":{"name":"Seltene genetische Krankheit der Retina"},"es":{"name":"Trastorno retiniano genético raro"},"it":{"name":"Patologia genetica rara retinica"},"nl":{"name":"Zeldzame genetische aandoening van retina","synonyms":["Zeldzame genetische aandoening van netvlies"]},"pt":{"name":"Doença retiniana genética rara"},"pl":{"name":"Rzadka choroba siatkówki uwarunkowana genetycznie"},"cs":{"name":"Vzácná genetická porucha sítnice"},"uk":{"name":"Рідкісне генетично обумовлене захворювання сітківки"},"zh":{"name":"罕见遗传性视网膜疾病"},"tr":{"name":"Nadir genetik retina bozukluğu"}},"xrefs":[{"source":"UMLS","code":"C5681407","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":71862,"name":"OBSOLETE: Inherited retinal disorder","status":"inactive"},{"type":"Referred to","orpha":98662,"name":"OBSOLETE: Unclassified familial retinal dystrophy","status":"inactive"},{"type":"Referred to","orpha":98664,"name":"OBSOLETE: Genetic macular dystrophy","status":"inactive"},{"type":"Referred to","orpha":98665,"name":"OBSOLETE: Colobomatous and areolar dystrophy","status":"inactive"},{"type":"Referred to","orpha":98666,"name":"OBSOLETE: Unclassified primitive or secondary maculopathy","status":"inactive"},{"type":"Referred to","orpha":227786,"name":"OBSOLETE: Familial flecked retinopathy","status":"inactive"},{"type":"Referred to","orpha":519306,"name":"OBSOLETE: Isolated progressive inherited retinal disorder","status":"inactive"},{"type":"Referred to","orpha":519319,"name":"OBSOLETE: Isolated stationary inherited retinal disorder","status":"inactive"},{"type":"Referred to","orpha":519325,"name":"OBSOLETE: Syndromic inherited retinal disorder","status":"inactive"},{"type":"Referred to","orpha":520817,"name":"OBSOLETE: Isolated inherited retinal disorder","status":"inactive"}],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":522570,"name":"Rare genetic disorder of the posterior segment of the eye","classifications":[156]}],"children":[{"orpha":717260,"name":"Rare genetic generalized retinal disorder","type":"Category"},{"orpha":522574,"name":"Rare genetic macular disorder","type":"Category"},{"orpha":717257,"name":"Rare genetic predominantly chorioretinal disorder","type":"Category"},{"orpha":522576,"name":"Rare genetic retinal vasculopathy","type":"Category"},{"orpha":98668,"name":"Vitreoretinopathy","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}