ORPHA:324927
Pyogenic autoinflammatory syndrome
- 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 | |
| fr | Syndrome auto-inflammatoire pyogène | |
| de | Autoinflammatorisches Syndrom, pyogenes | |
| es | Síndrome autoinflamatorio piogénico | |
| it | Sindrome autoinfiammatoria piogenica | |
| nl | Pyogeen auto-inflammatoir syndroom | |
| pt | Síndrome autoinflamatória piogénica | |
| pl | Zespół autozapalenia ropnego | |
| cs | Pyogenní autoinflamatorní onemocnění | |
| uk | Піогенний аутозапальний синдром | |
| zh | 化脓性自身炎症综合征 | |
| tr | Piyojenik otoinflamatuar sendrom |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17954 | E | validated | |
| UMLS | C5680956 | 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:54251Aseptic abscess syndrome
- ORPHA:653434Autoinflammatory syndrome with acne and/or hidradenitis suppurativa
- 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:48104Pyoderma gangrenosum
- ORPHA:210115Sterile multifocal osteomyelitis with periostitis and pustulosis
- ORPHA:3243Sweet syndrome
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/324927
- This record as JSON: /data/d/324927.json