raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93956

OBSOLETE: Truncal dystonia

inactive · referred to ORPHA:1866Focal, segmental or multifocal dystonia

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Focal, segmental or multifocal dystonia

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Truncal dystonia
frOBSOLETE : Dystonie du tronc
deOBSOLET: Rumpfdystonie
esOBSOLETO: Distonía de tronco
itOBSOLETO: Distonia del tronco
nlOBSOLEET: Rompdystonie
ptOBSOLETO: Distonia do tronco
plNIEAKTUALNE: Dystonia tulowia
csNEAKTUÁLNÍ: Trunkální dystonie
ukЗАСТАРІЛО: Трункальна дистонія
zh弃用:躯干肌张力障碍
trEski adı: Trunkal distoni
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