ORPHA:324942
Pyogenic autoinflammatory syndrome of childhood
- Type
- Category
- Group
- Group of disorders
- 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 | Pyogenic autoinflammatory syndrome of childhood | |
| fr | Syndrome auto-inflammatoire pyogène de l'enfant | |
| de | Autoinflammatorisches Syndrom, pyogenes, der Kindheit | |
| es | Síndrome autoinflamatorio piogénico de la infancia | |
| it | Sindrome autoinfiammatoria piogenica dell'infanzia | |
| nl | Pyogeen auto-inflammatoir syndroom van de kinderjaren | |
| pt | Síndrome autoinflamatória piogénica da infância | |
| pl | Dziecięcy zespół autozapalenia ropnego | |
| cs | Pyogenní autoinflamatorní syndrom v dětství | |
| uk | Піогенний аутозапальний синдром дитячого віку | |
| zh | 儿童化脓性自体炎症综合征 | |
| tr | Çocukluk çağı piyojenik otoinflamatuvar sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0957404 | E | validated | |
| UMLS | C5680953 | 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:319719Autoinflammatory syndrome of childhood
rare systemic or rheumatologic diseases of childhood
Children (7):
- ORPHA:324964Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis
- ORPHA:404546DITRA
- ORPHA:251523Hyperzincemia and hypercalprotectinemia
- ORPHA:77297Majeed syndrome
- ORPHA:294023Neonatal erythroderma-autoinflammation-inflammatory bowel disease syndrome
- ORPHA:69126PAPA syndrome
- ORPHA:210115Sterile multifocal osteomyelitis with periostitis and pustulosis
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/324942
- This record as JSON: /data/d/324942.json