ORPHA:324936
Unclassified autoinflammatory syndrome
- Type
- Category
- Group
- Group of disorders
- Age of onset
- Antenatal, Infancy, Neonatal
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Unclassified autoinflammatory syndrome | |
| fr | Syndrome auto-inflammatoire non classé | |
| de | Autoinflammatorisches Syndrom, unklassifiziertes | |
| es | Síndrome autoinflamatorio no clasificado | |
| it | Sindrome autoinfiammatoria non classificata | |
| nl | Niet-geclassificeerd auto-inflammatoir syndroom | |
| pt | Síndrome autoinflamatória não classificada | |
| pl | Niesklasyfikowany zespół autozapalenia | |
| cs | Neklasifikovaný autoinflamatorní syndrom | |
| uk | Некласифікований аутозапальний синдром | |
| zh | 未分类的自身炎症综合征 | |
| tr | Sınıflandırılmamış otoinflamatuar sendrom |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17957 | E | validated | |
| UMLS | C5680959 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:93665Autoinflammatory syndrome
rare systemic and rheumatological diseases
Children (10):
- ORPHA:117Behçet disease
- ORPHA:184Cherubism
- ORPHA:674762Early-onset autoinflammatory syndrome due to A20 haploinsufficiency
- ORPHA:251307Idiopathic recurrent pericarditis
- ORPHA:324972MAGIC syndrome
- ORPHA:619363NOCARH syndrome
- ORPHA:596759RELA haploinsufficiency-associated inflammatory disease
- ORPHA:723218SITRAME Syndrome
- ORPHA:596753VEXAS syndrome
- ORPHA:676125X-linked immune dysregulation with inflammatory bowel disease due to ELF4 deficiency
Codes that Orphanet moved or referred to this one:
- ORPHA:476102OBSOLETE: Hereditary pediatric Behçet-like disease referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/324936
- This record as JSON: /data/d/324936.json