ORPHA:97966
Rare ophthalmic disorder
- Type
- Category
- Group
- Group of disorders
- Status
- active
- Flag
- Head of classification
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 ophthalmic disorder | |
| fr | Maladie ophtalmique rare | |
| de | Augenkrankheit, seltene | |
| es | Trastorno oftalmológico raro | |
| it | Malattia oculare rara | |
| nl | Zeldzame oftalmische stoornis | |
| pt | Doença oftalmológica rara | |
| pl | Rzadkie choroby oczu | |
| cs | Vzácná onemocnění oka | |
| uk | Рідкісне офтальмологічне захворювання | |
| zh | 罕见视力异常 | |
| tr | Nadir görülen oftalmik bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681556 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Not placed in any Orphanet classification in this release.
Codes that Orphanet moved or referred to this one:
- ORPHA:2120OBSOLETE: Heckenlively syndrome referred to · inactive
- ORPHA:71269OBSOLETE: Benign exophthalmos syndrome referred to · inactive
- ORPHA:101949OBSOLETE: Rare acquired eye disease referred to · inactive
- ORPHA:182214OBSOLETE: Rare inflammatory eye disease referred to · inactive
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/97966
- This record as JSON: /data/d/97966.json