ORPHA:652510
Genetic autoinflammatory syndrome with acne and/or hidradenitis suppurativa
- Type
- Clinical group
- 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
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Genetic autoinflammatory syndrome with acne and/or hidradenitis suppurativa | |
| fr | Syndrome génétique autoinflammatoire avec acné et/ou hidradénite suppurée | |
| de | Autoinflammatorisches Syndrom mit Akne und/oder Hidradenitis suppurativa, genetisch bedingtes | |
| es | Síndrome autoinflamatorio genético con acné y/o hidradenitis supurativa | |
| it | Sindrome genetica autoinfiammatoria con acne e/o idrosadenite suppurativa | |
| nl | Genetisch auto-inflammatoir syndroom met acne en/of hidradenitis suppurativa | |
| pt | Síndrome autoinflamatório genético com acne e/ou hidradenite supurativa | |
| pl | Genetycznie uwarunkowany zespół autozapalny z trądzikiem i/lub ropnym zapaleniem gruczołów potowych | |
| cs | Genetický autoinflamatorní syndrom s akné a/nebo hidradenitis suppurativa | |
| uk | Генетично обумовлений аутозапальний синдром з акне та/або гнійним гідраденітом |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5925118 | 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 (2):
- ORPHA:622720Genetic autoinflammatory syndrome with skin involvement
rare genetic diseases - ORPHA:619238Rare hereditary autoinflammatory disease
rare genetic 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/652510
- This record as JSON: /data/d/652510.json