raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:293848

Frontotemporal dementia, right temporal atrophy variant

inactive · moved to ORPHA:282Frontotemporal dementia

Synonyms: RTLA · rvFTD

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Frontotemporal dementia

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enFrontotemporal dementia, right temporal atrophy variantRTLA · rvFTD
frDémence fronto-temporale, variante d'atrophie temporale à droite= en
deFrontotemporale Demenz, rechtstemporale Variante= en
esDemencia frontotemporal, variante con atrofia temporal derecha= en
itDemenza frontotemporale, variante dell'atrofia temporale destra= en
nlFrontotemporale dementie, rechter temporale atrofie variant= en
ptAtrofia lobar temporal direitaDemência frontotemporal, variante atrofia temporal direita · RTLA · rvFTD
plZanik prawego płata skroniowegoOtępienie czołowo-skroniowe, wariant zanik skroniowy prawy · RTLA · rvFTD
csFrontotemporální demence, varianta s temporální atrofií vpravo= en
ukЛобно-скронева деменція, варіант правої скроневої атрофії= en
zh右侧颞叶萎缩变异型额颞叶痴呆右侧颞叶萎缩变异型额颞叶痴呆
trFrontotemporal demans, sağ temporal atrofi varyantı= en

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card