{"orpha":98572,"name":"OBSOLETE: Canthal anomaly","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 palpebral disorder","url":"https://raremap.alftech.space/d/ORPHA-98572/","orphanet_url":"https://www.orpha.net/en/disease/detail/98572","names":{"fr":{"name":"OBSOLETE : Anomalie des canthus"},"de":{"name":"OBSOLET: Lidwinkel-Anomalie"},"es":{"name":"OBSOLETO: Anomalía cantal"},"it":{"name":"OBSOLETO: Anomalia cantale"},"nl":{"name":"OBSOLEET: Canthale anomalie"},"pt":{"name":"OBSOLETO: Anomalia cantal"},"pl":{"name":"NIEAKTUALNE: Anomalia kata oka"},"cs":{"name":"NEAKTUÁLNÍ: Anomálie očních koutků"},"uk":{"name":"ЗАСТАРІЛО: Кантальна аномалія"},"zh":{"name":"弃用：眦异常"},"tr":{"name":"Eski adı: Kantal anomali"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":98560,"name":"Rare palpebral disorder"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}