raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2042

OBSOLETE: Tracheo-esophageal fistula-hypospadias syndrome

inactive · referred to ORPHA:1199Esophageal atresia

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Obsolete entity

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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Tracheo-esophageal fistula-hypospadias syndrome
frOBSOLETE : Syndrome de fistule trachéo-oesophagienne-hypospadias
deOBSOLET: Hypospadie - Tracheophagealfistel
esOBSOLETO: Síndrome de fístula traqueofágica-hipospadias
itOBSOLETO: Fistola tracheoesofagea - ipospadia
nlOBSOLEET: Tracheo-oesofageale fistel - hypospadie-syndroom
ptOBSOLETO: Síndrome de fístula traqueo-esofágica-hipospadias
plNIEAKTUALNE: Przetoka tchawiczo-przelykowa - spodziectwo
csNEAKTUÁLNÍ: Syndrom zahrnující tracheoezofageální píštěl a hypospadii
ukЗАСТАРІЛО: Синдром трахео-стравохідної нориці-гіпоспадії
zh弃用:气管-食管瘘-尿道下裂综合征
trEski adı: Trakeo-özofageal fistül-hipospadias 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