ORPHA:93365
OBSOLETE: CINCA syndrome with 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
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: CINCA syndrome with NLRP3 mutations | |
| fr | OBSOLETE : Syndrome CINCA avec mutation de NLRP3 | |
| de | OBSOLET: CINCA-Syndrom mit NLRP3-Genmutationen | |
| es | OBSOLETO: Síndrome CINCA con mutaciones en el gen NLRP3 | |
| it | OBSOLETO: Sindrome CINCA con mutazioni di NLRP3 | |
| nl | OBSOLEET: CINCA-syndroom met NLRP3-mutaties | |
| pt | OBSOLETO: Síndrome CINCA com mutações no gene CIAS1 | |
| pl | NIEAKTUALNE: Zespól CINCA z mutacjami NLRP3 | |
| cs | NEAKTUÁLNÍ: Syndrom CINCA s mutacemi NLRP3 | |
| uk | ЗАСТАРІЛО: Синдром CINCA з мутаціями NLRP3 | |
| zh | 弃用：伴有NLRP3突变的CINCA综合征 | |
| tr | Eski adı: NLRP3 mutasyon ile seyreden CINCA sendromu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/93365
- This record as JSON: /data/d/93365.json