raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1396

OBSOLETE: Cerebrorenodigital syndrome

inactive · referred to ORPHA:564Meckel syndrome

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 Meckel syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Cerebrorenodigital syndrome
frOBSOLETE : Syndrome cérébrorénodigital
deOBSOLET: Zerebro-reno-digitales Syndrom
esOBSOLETO: Síndrome cerebro-reno-digital
itOBSOLETO: Sindrome cerebro-reno-digitaleOBSOLETO: Sindrome Meckel-simile
nlOBSOLEET: Cerebro-reno-digitaal syndroom
ptOBSOLETO: Síndrome cerebro-reno-digitalOBSOLETO: Síndrome Meckel-like
plNIEAKTUALNE: Zespól mózgowo-nerkowo-palcowy
csNEAKTUÁLNÍ: Cerebrorenodigitální syndrom
ukЗАСТАРІЛО: Цереброренодигітальний синдром
zh弃用:脑-肾-指综合征
trEski adı: Serebrorenodijital sendrom
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