ORPHA:648559
Rare scleritis
- 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 | Rare scleritis | |
| fr | Sclérite rare | |
| de | Seltene Skleritis | |
| es | Escleritis rara | |
| it | Sclerite rara | |
| nl | Zeldzame scleritis | |
| pt | Esclerite rara | |
| pl | Rzadkie zapalenie twardówki | |
| cs | Vzácná skleritida | |
| uk | Рідкісний склероз |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5816743 | 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:519298Rare scleral disorder
rare ophthalmic disorders
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/648559
- This record as JSON: /data/d/648559.json