raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:101042

OBSOLETE: Taussig-Bing syndrome

inactive · referred to ORPHA:99045Double outlet right ventricle with subpulmonary ventricular septal defect

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 Double outlet right ventricle with subpulmonary ventricular septal defect

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Taussig-Bing syndrome
frOBSOLETE : Syndrome de Taussig-Bing
deOBSOLET: Taussig-Bing-Syndrom
esOBSOLETO: Síndrome de Taussig-Bing
itOBSOLETO: Sindrome di Taussig-Bing
nlOBSOLEET: Taussig-Bingsyndroom
ptOBSOLETO: Síndrome Taussig-Bing
plNIEAKTUALNE: Zespól Taussig i Binga
csNEAKTUÁLNÍ: Taussig-Bingův syndrom
ukЗАСТАРІЛО: Синдром Таусіга-Бінга
zh弃用:陶-宾综合征
trEski adı: Taussig-Bing 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