{"orpha":2120,"name":"OBSOLETE: Heckenlively syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Rare ophthalmic disorder","url":"https://raremap.alftech.space/d/ORPHA-2120/","orphanet_url":"https://www.orpha.net/en/disease/detail/2120","names":{"fr":{"name":"OBSOLETE : Syndrome de Heckenlively"},"de":{"name":"OBSOLET: Heckenlively-Syndrom"},"es":{"name":"OBSOLETO: Síndrome de Heckenlively"},"it":{"name":"OBSOLETO: Sindrome di Heckenlively"},"nl":{"name":"OBSOLEET: Syndroom van Heckenlively"},"pt":{"name":"OBSOLETO: Síndrome Heckenlively"},"pl":{"name":"NIEAKTUALNE: Zespól Heckenlively"},"cs":{"name":"NEAKTUÁLNÍ: Heckenlivelyho syndrom"},"uk":{"name":"ЗАСТАРІЛО: Синдром Хекенлівлі"},"zh":{"name":"弃用：Heckenlively综合征"},"tr":{"name":"Eski adı: Heckenlively sendromu"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":97966,"name":"Rare ophthalmic disorder"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}