raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93975

OBSOLETE: Renier-Gabreels-Jasper syndrome

inactive · referred to ORPHA:528084Non-specific syndromic intellectual disability

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-specific syndromic intellectual disability

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Renier-Gabreels-Jasper syndrome
frOBSOLETE : Syndrome de Renier-Gabreels-Jasper
deOBSOLET: Renier-Gabreels-Jasper-Syndrom
esOBSOLETO: Síndrome de Renier-Gabreels-Jasper
itOBSOLETO: Sindrome di Renier-Gabreels-Jasper
nlOBSOLEET: Syndroom van Renier-Gabreels-Jasper
ptOBSOLETO: Síndrome Renier-Gabreels-Jasper
plNIEAKTUALNE: Zespół Reniera, Gabreelsa i Jaspera
csNEAKTUÁLNÍ: Renierův-Gabreelsův-Jasperův syndromNEAKTUÁLNÍ: Renier-Gabreels-Jasperův syndrom
ukЗАСТАРІЛО: Синдром Реньє-Габрельса-Джаспера
zhRenier-Gabreels-Jasper综合征
trRenier-Gabreels-Jasper 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