{"orpha":716358,"name":"Rare generalized 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-716358/","orphanet_url":"https://www.orpha.net/en/disease/detail/716358","names":{"fr":{"name":"Maladie rare rétinienne généralisée"},"de":{"name":"Seltene generalisierte Retinopathie"},"es":{"name":"Trastorno retiniano generalizado raro"},"it":{"name":"Retinopatia generalizzata rara"},"nl":{"name":"Zeldzame gegeneraliseerde aandoening van retina"},"pt":{"name":"Rare generalized retinal disorder"},"pl":{"name":"Rzadkie uogólnione zaburzenie siatkówki"},"cs":{"name":"Rare generalized retinal disorder"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":519315,"name":"Rare retinal disorder","classifications":[189]}],"children":[{"orpha":716364,"name":"Rare non-progressive generalized retinal disorder","type":"Category"},{"orpha":716361,"name":"Rare progressive generalized retinal disorder","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}