ORPHA:519298
Rare scleral 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 scleral disorder | |
| fr | Maladie rare de la sclérotique | |
| de | Seltene Krankheit der Sklera | |
| es | Trastorno raro de la esclerótica | |
| it | Patologia sclerale rara | |
| nl | Zeldzame aandoening van sclera | |
| pt | Doença rara da esclera | |
| pl | Rzadka choroba twardówki | |
| cs | Vzácná porucha skléry | |
| uk | Рідкісний склеральний розлад | |
| zh | 罕见的巩膜病变 | |
| tr | Nadir skleral bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681369 | 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:520814Rare disorder of the visual organs
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/519298
- This record as JSON: /data/d/519298.json