raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98932

OBSOLETE: Shy-Drager syndrome

inactive · referred to ORPHA:102Multiple system atrophy

Synonyms: OBSOLETE: MSA-urinary dysfunction syndrome · OBSOLETE: Multiple system atrophy-urinary dysfunction syndrome

Type
Clinical subtype
Group
Subtype of disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Multiple system atrophy

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Shy-Drager syndromeOBSOLETE: MSA-urinary dysfunction syndrome · OBSOLETE: Multiple system atrophy-urinary dysfunction syndrome
frOBSOLETE : Syndrome de Shy-DragerOBSOLETE : Atrophie multisystématisée-trouble urinaire · OBSOLETE : SDS · OBSOLETE : AMS-trouble urinaire
deOBSOLET: Shy-Drager-SyndromOBSOLET: Multiple Systematrophie-Harnfunktionsstörung-Syndrom
esOBSOLETO: Síndrome de Shy-DragerOBSOLETO: Síndrome de disfunción urinaria-AMS · OBSOLETO: Síndrome de disfunción urinaria-atrofia multisistémica
itOBSOLETO: Sindrome di Shy-DragerOBSOLETO: Sindrome MSA-disfunzione urinaria · OBSOLETO: Sindrome atrofia multisistemica-disfunzione urinaria
nlOBSOLEET: Syndroom van Shy-DragerOBSOLEET: MSA - urinaire disfunctie · OBSOLEET: Meervoudige systeematrofie - urinaire disfunctie · OBSOLEET: SDS
ptOBSOLETO: Síndrome Shy-Drager
plNIEAKTUALNE: Zespól Shy'a i DrageraNIEAKTUALNE: MSA - urinary dysfunction · NIEAKTUALNE: SDS · NIEAKTUALNE: Zanik wieloukładowy - dysfunkcja układu moczowego
csNEAKTUÁLNÍ: Shy-Dragerův syndrom= en
ukЗАСТАРІЛО: Синдром Шай-ДрегераЗАСТАРІЛО: Синдром MСA-дисфункції сечовидільної системи · ЗАСТАРІЛО: Синдром множинної системної атрофії-сечової дисфункції
zh弃用:Shy-Drager 综合征多系统萎缩-排尿功能障碍综合征
trEski adı: Shy-Drager sendromuMSA-üriner disfonksiyon sendromu · Çoklu sistem atrofi-üriner disfonksiyon sendromu
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