ORPHA:519290
Rare inflammatory/autoimmune corneal disorder
- 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 | Rare inflammatory/autoimmune corneal disorder | |
| fr | Maladie cornéenne auto-inflammatoire ou auto-immune | |
| de | Seltene entzündliche/autoimmune Krankheit der Kornea | |
| es | Trastorno raro corneal inflamatorio/autoinmune | |
| it | Patologia rara corneale infiammatoria/autoimmune | |
| nl | Zeldzame inflammatoire/auto-immune aandoening van cornea | Zeldzame inflammatoire/auto-immune aandoening van hoornvlies |
| pt | Doença da córnea inflamatória/autoimune rara | |
| pl | Rzadka choroba zapalna/autoimmunologiczna rogówki | |
| cs | Vzácná zánětlivá/autoimunitní porucha rohovky | |
| uk | Рідкісне запальне/аутоімунне захворювання рогівки | |
| zh | 罕见的炎症/自身免疫性角膜疾病 | |
| tr | Nadir inflamatuar/otoimmün kornea bozukluğu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681389 | 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:519288Rare disorder with corneal involvement as a major feature
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/519290
- This record as JSON: /data/d/519290.json