{"orpha":3336,"name":"TomÚ-Brunet-Fardeau syndrome","type":"Malformation syndrome","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 ATP13A2-related juvenile neuronal ceroid lipofuscinosis","url":"https://raremap.alftech.space/d/ORPHA-3336/","orphanet_url":"https://www.orpha.net/en/disease/detail/3336","names":{"fr":{"name":"Syndrome de Tomé-Brunet-Fardeau"},"de":{"name":"Tome-Brune-Fardeau-Syndrom"},"es":{"name":"Síndrome de Tomé-Brunet-Fardeau"},"it":{"name":"Sindrome di Tome-Brune-Fardeau"},"nl":{"name":"Syndroom van Tomé-Brunet-Fardeau"},"pt":{"name":"Síndrome Tomé-Brune-Fardeau"},"pl":{"name":"Zespół Tomé, Bruneta i Fardeau"},"cs":{"name":"Tomého-Brunetův-Fardeauův syndrom","synonyms":["Tomé-Brunet-Fardeauův syndrom"]},"uk":{"name":"Синдром Томю-Брюне-Фардо"},"zh":{"name":"TomÚ-Brunet-Fardeau 综合征"},"tr":{"name":"Tomé-Brunet-Fardeau sendromu"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":314632,"name":"CLN12 disease"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}