{"orpha":98941,"name":"OBSOLETE: Von Hippel anomaly","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 Congenital glaucoma","url":"https://raremap.alftech.space/d/ORPHA-98941/","orphanet_url":"https://www.orpha.net/en/disease/detail/98941","names":{"fr":{"name":"OBSOLETE : Anomalie de von Hippel"},"de":{"name":"OBSOLET: Von-Hippel-Anomalie"},"es":{"name":"OBSOLETO: Anomalía de Von Hippel"},"it":{"name":"OBSOLETO: Anomalia di von Hippel"},"nl":{"name":"OBSOLEET: Von Hippel-anomalie"},"pt":{"name":"OBSOLETO: Anomalia de von Hippel"},"pl":{"name":"NIEAKTUALNE: Anomalia von Hippela"},"cs":{"name":"NEAKTUÁLNÍ: Von Hippelova anomálie"},"uk":{"name":"ЗАСТАРІЛО: Аномалія фон Гіппеля"},"zh":{"name":"弃用：希佩尔异常"},"tr":{"name":"Eski adı: Von Hippel anomalisi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":98976,"name":"Congenital glaucoma"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}