raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1849

OBSOLETE: Infundibulopelvic stenosis-multicystic kidney syndrome

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

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 Non-syndromic renal or urinary tract malformation

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Infundibulopelvic stenosis-multicystic kidney syndrome
frOBSOLETE : Syndrome de dysplasie rénale autosomique dominante-sténose infundibulo-pelvienne
deOBSOLET: Ureterabgangstenose - polyzystische Nierendegeneration
esOBSOLETO: Síndrome de estenosis infundibulopélvica-riñón multiquístico
itOBSOLETO: Sindrome stenosi infundibolo-pelvica - rene policistico
nlOBSOLEET: Infundibulopelvisstenose - multicystische nier-syndroom
ptOBSOLETO: Síndrome de estenose infundibulopélvica-rim multiquístico
plNIEAKTUALNE: Stenoza lejkowo-miedniczna - wielotorbielowata nerka
csNEAKTUÁLNÍ: Syndrom zahrnující infundibulopelvickou stenózu a multicystickou dysplázii ledviny
ukЗАСТАРІЛО: Синдром інфундибулопельвікального стенозу - полікістозу нирок
zh弃用:肾盂肾下盏漏斗狭窄-多囊肾综合征
trEski adı: İnfundibulopelvik stenoz-multikistik böbrek 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