{"orpha":293848,"name":"Frontotemporal dementia, right temporal atrophy variant","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["RTLA","rvFTD"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Frontotemporal dementia","url":"https://raremap.alftech.space/d/ORPHA-293848/","orphanet_url":"https://www.orpha.net/en/disease/detail/293848","names":{"fr":{"name":"Démence fronto-temporale, variante d'atrophie temporale à droite","synonyms":["RTLA","rvFTD"]},"de":{"name":"Frontotemporale Demenz, rechtstemporale Variante","synonyms":["RTLA","rvFTD"]},"es":{"name":"Demencia frontotemporal, variante con atrofia temporal derecha","synonyms":["RTLA","rvFTD"]},"it":{"name":"Demenza frontotemporale, variante dell'atrofia temporale destra","synonyms":["RTLA","rvFTD"]},"nl":{"name":"Frontotemporale dementie, rechter temporale atrofie variant","synonyms":["RTLA","rvFTD"]},"pt":{"name":"Atrofia lobar temporal direita","synonyms":["Demência frontotemporal, variante atrofia temporal direita","RTLA","rvFTD"]},"pl":{"name":"Zanik prawego płata skroniowego","synonyms":["Otępienie czołowo-skroniowe, wariant zanik skroniowy prawy","RTLA","rvFTD"]},"cs":{"name":"Frontotemporální demence, varianta s temporální atrofií vpravo","synonyms":["RTLA","rvFTD"]},"uk":{"name":"Лобно-скронева деменція, варіант правої скроневої атрофії","synonyms":["RTLA","rvFTD"]},"zh":{"name":"右侧颞叶萎缩变异型额颞叶痴呆","synonyms":["右侧颞叶萎缩变异型额颞叶痴呆"],"definition":"右颞部脑叶萎缩（RTLA）是额颞叶痴呆（FTD）的解剖学变异，其特征是行为功能障碍、个性改变、阵发性记忆丧失和面孔失认症。本病主要由于不对称的右侧额颞叶萎缩所致。"},"tr":{"name":"Frontotemporal demans, sağ temporal atrofi varyantı","synonyms":["RTLA","rvFTD"]}},"xrefs":[],"associations":[{"type":"Moved to","orpha":282,"name":"Frontotemporal dementia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}