raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2190

OBSOLETE: Congenital hydronephrosis

inactive · referred to ORPHA:93546Non-syndromic renal or urinary tract malformation

Type
Morphological anomaly
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Non-syndromic renal or urinary tract malformation

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Congenital hydronephrosis
frOBSOLETE : Hydronéphrose congénitale
deOBSOLET: Hydronephrose, kongenitale
esOBSOLETO: Hidronefrosis congénita
itOBSOLETO: Idronefrosi congenita
nlOBSOLEET: Congenitale hydronefrose
ptOBSOLETO: Hidronefrose congénita
plNIEAKTUALNE: Wrodzone wodonercze
csNEAKTUÁLNÍ: Vrozená hydronefróza
ukЗАСТАРІЛО: Вроджений гідронефроз
zh弃用:先天性肾盂积水
trEski adı: Doğumsal hidronefroz
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