raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93367

OBSOLETE: CINCA syndrome without NLRP3 mutations

inactive · referred to ORPHA:1451CINCA 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 CINCA syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: CINCA syndrome without NLRP3 mutations
frOBSOLETE : Syndrome CINCA sans mutation de NLRP3
deOBSOLET: CINCA-Syndrom ohne NLRP3-Genmutationen
esOBSOLETO: Síndrome CINCA sin mutaciones en el gen NLRP3
itOBSOLETO: Sindrome CINCA senza mutazioni del gene NLRP3
nlOBSOLEET: CINCA-syndroom zonder NLRP3-mutaties
ptOBSOLETO: Síndrome CINCA sem mutações no gene CIAS1
plNIEAKTUALNE: Zespól CINCA bez mutacjit NLRP3
csNEAKTUÁLNÍ: Syndrom CINCA bez mutací NLRP3
ukЗАСТАРІЛО: Синдром CINCA без мутацій NLRP3
zh弃用:不伴有NLRP3突变的CINCA综合征
trEski adı: NLRP3 mutasyonları olmayan CINCA 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