raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93178

OBSOLETE: Partial prune belly syndrome

inactive · referred to ORPHA:2970Prune belly 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 Prune belly syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Partial prune belly syndrome
frOBSOLETE : Syndrome de prune belly partiel
deOBSOLET: Prune-Belly-Syndrom, partielles
esOBSOLETO: Síndrome de abdomen en ciruela pasa, forma parcial
itOBSOLETO: Sindrome ''prune belly'', forma parziale
nlOBSOLEET: Partiële prune belly-syndroom
ptOBSOLETO: Barriga de ameixa seca (prune belly), síndrome, forma parcial
plNIEAKTUALNE: Czesciowy zespól suszonej sliwki
csNEAKTUÁLNÍ: Částečný prune belly syndrom
ukЗАСТАРІЛО: Синдром часткового сливового живота
zh弃用:部分梨状腹综合征
trEski adı: Kısmi erik göbek 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