raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98204

OBSOLETE: Heredodegenerative disease with dystonia as a major feature

inactive · referred to ORPHA:102003Rare movement disorder

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Rare movement disorder

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Heredodegenerative disease with dystonia as a major feature
frOBSOLETE : Maladie hérédo-dégénérative avec dystonie comme manifestation majeure
deOBSOLET: Heredodegenerative Krankheit mit assoziierter Dystonie
esOBSOLETO: Enfermedad heredodegenerativa con distonía como manifestación principal
itOBSOLETO: Malattia eredodegenerativa con distonia come segno principale
nlOBSOLEET: Heredodegeneratieve ziekte met dystonie als hoofdkenmerk
ptOBSOLETO: Doença heredodegenerativa com distonia como característica principal
plNIEAKTUALNE: Choroba neurodegeneracyjna z dystonia jako glównym objawem
csNEAKTUÁLNÍ: Dědičně-degenerativní onemocnění s dystonií jako hlavním rysem
ukЗАСТАРІЛО: Спадково-дегенеративне захворювання з дистонією як основною ознакою
zh弃用:以肌张力障碍为主要表现遗传退行性疾病
trEski adı:Esas klinik özelliği distoni olan heredodejeneratif hastalık
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