{"orpha":338,"name":"Familial multiple fibrofolliculoma","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Birt-Hogg-Dubé syndrome","url":"https://raremap.alftech.space/d/ORPHA-338/","orphanet_url":"https://www.orpha.net/en/disease/detail/338","names":{"fr":{"name":"Fibrofolliculomes multiples familiaux"},"de":{"name":"Fibrofollikulom, familiäres multiples"},"es":{"name":"Fibrofoliculomas múltiples familiares"},"it":{"name":"Fibrofolliculomi multipli familiari"},"nl":{"name":"Familiaal meervoudig fibrofolliculoom"},"pt":{"name":"Fibrofoliculoma múltiplo familiar"},"pl":{"name":"Rodzinne mnogie włókniakoziarniszczaki"},"cs":{"name":"Familiární mnohočetný fibrofolikulom"},"uk":{"name":"Сімейна множинна фіброфолікулома"},"zh":{"name":"家族性多发性纤维毛囊瘤"},"tr":{"name":"Ailesel çoklu fibrofolikülom"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":122,"name":"Birt-Hogg-Dubé syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}