ORPHA:98621
Rare hyperopia and astigmatism
- 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 hyperopia and astigmatism | |
| fr | Hypermétropie et astigmatisme rares | |
| de | Hyperopie und Astigmatismus, selten | |
| es | Hipermetropía y astigmatismo raros | |
| it | Iperopia e astigmatismo rari | |
| nl | Zeldzame hyperopie en astigmatisme | |
| pt | Hiperopia e astigmatismo, raros | |
| pl | Rzadka dalekowzroczność i astygmatyzm | |
| cs | Vzácná onemocnění s hyperopií a/nebo astigmatismem | |
| uk | Рідкісна далекозорість та астигматизм | |
| zh | 罕见远视和散光 | |
| tr | Nadir hipermetrop ve astigmat |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681676 | 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:98618Rare refraction anomaly
rare genetic diseases; 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/98621
- This record as JSON: /data/d/98621.json