{"orpha":719766,"name":"Photic retinopathy","type":"Disease","group":"Disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-719766/","orphanet_url":"https://www.orpha.net/en/disease/detail/719766","names":{"fr":{"name":"Rétinopathie photique"},"de":{"name":"Photische Retinopathie","synonyms":["Solarretinopathie","Retinopathia solaris","Solare Retinopathie"]},"es":{"name":"Retinopatía fótica"},"it":{"name":"Fotoretinopatia"},"nl":{"name":"Retinopathie door ultraviolette straling","synonyms":["Retinopathie door UV-straling"]},"pt":{"name":"Rétinopathie photique"},"pl":{"name":"Photic retinopathy"},"cs":{"name":"Photic retinopathy"}},"xrefs":[{"source":"ICD-10","code":"H31.0","qualifier":"NTBT","icd_relation":"attributed","validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":716419,"name":"Rare isolated non-progressive predominantly macular disorder","classifications":[189]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":["All ages"],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Validated","source":"ORPHANET"}],"phenotypes":null}