{"orpha":98658,"name":"Color-vision disease","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-98658/","orphanet_url":"https://www.orpha.net/en/disease/detail/98658","names":{"fr":{"name":"Trouble de la vision des couleurs"},"de":{"name":"Farbsehstörung"},"es":{"name":"Enfermedad de la visión de los colores"},"it":{"name":"Malattia della visione a colori"},"nl":{"name":"Kleurwaarnemingsziekte"},"pt":{"name":"Doença da visão cromática"},"pl":{"name":"Choroba rozróżniania kolorów"},"cs":{"name":"Poruchy barevného vidění"},"uk":{"name":"Захворювання кольорового зору"},"zh":{"name":"颜色-视觉疾病"},"tr":{"name":"Renk körlüğü hastalığı"}},"xrefs":[{"source":"ICD-10","code":"H53.5","qualifier":"E","icd_relation":"specific","validated":true},{"source":"MONDO","code":"0001703","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"1703","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681659","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":101435,"name":"Rare genetic eye disease","classifications":[156]},{"orpha":97966,"name":"Rare ophthalmic disorder","classifications":[189]}],"children":[{"orpha":49382,"name":"Achromatopsia","type":"Disease"},{"orpha":16,"name":"Blue cone monochromatism","type":"Disease"},{"orpha":88629,"name":"Tritanopia","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}