ORPHA:324930
Granulomatous 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 | Granulomatous autoinflammatory syndrome | |
| fr | Syndrome auto-inflammatoire granulomateux | |
| de | Autoinflammatorisches Syndrom, granulomatöses | |
| es | Síndrome autoinflamatorio granulomatoso | |
| it | Sindrome autoinfiammatoria granulomatosa | |
| nl | Granulomateus auto-inflammatoir syndroom | |
| pt | Síndrome autoinflamatória granulomatosa | |
| pl | Zespół autozapalenia ziarniniakowego | |
| cs | Granulomatózní autoinflamatorní syndrom | |
| uk | Гранулематозний аутозапальний синдром | |
| zh | 肉芽肿性自身炎症综合征 | |
| tr | Granülomatöz otoinflamatuar sendrom |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17955 | E | validated | |
| UMLS | C5680957 | 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
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/324930
- This record as JSON: /data/d/324930.json