{"orpha":68388,"name":"OBSOLETE: Neurofibromatosis","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 Malformation syndrome with hamartosis","url":"https://raremap.alftech.space/d/ORPHA-68388/","orphanet_url":"https://www.orpha.net/en/disease/detail/68388","names":{"fr":{"name":"OBSOLETE : Neurofibromatose"},"de":{"name":"OBSOLET: Neurofibromatose"},"es":{"name":"OBSOLETO: Neurofibromatosis"},"it":{"name":"OBSOLETO: Neurofibromatosi"},"nl":{"name":"OBSOLEET: Neurofibromatose"},"pt":{"name":"OBSOLETO: Neurofibromatose"},"pl":{"name":"NIEAKTUALNE: Neurofibromatoza"},"cs":{"name":"NEAKTUÁLNÍ: Neurofibromatóza"},"uk":{"name":"ЗАСТАРІЛО: Нейрофіброматоз"},"zh":{"name":"弃用：神经纤维瘤病"},"tr":{"name":"Eski adı: Nörofibromatoz"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":98196,"name":"Malformation syndrome with hamartosis"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}