{"orpha":98620,"name":"OBSOLETE: Syndromic myopia","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare refraction anomaly","url":"https://raremap.alftech.space/d/ORPHA-98620/","orphanet_url":"https://www.orpha.net/en/disease/detail/98620","names":{"fr":{"name":"OBSOLETE : Myopie syndromique"},"de":{"name":"OBSOLET: Myopie, syndromale"},"es":{"name":"OBSOLETO: Miopía sindrómica"},"it":{"name":"OBSOLETO: Miopia sindromica"},"nl":{"name":"OBSOLEET: Syndromale myopie"},"pt":{"name":"OBSOLETO: Miopia sindromática"},"pl":{"name":"NIEAKTUALNE: Krótkowzrocznosc syndromiczna"},"cs":{"name":"NEAKTUÁLNÍ: Syndromy s myopií"},"uk":{"name":"ЗАСТАРІЛО: Синдромальна короткозорість"},"zh":{"name":"弃用：综合征型近视"},"tr":{"name":"Eski adı: Sendromik miyopi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":98618,"name":"Rare refraction anomaly"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}