ORPHA:98618
Rare refraction anomaly
- 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 refraction anomaly | |
| fr | Anomalie rare de la réfraction | |
| de | Refraktionsstörung, seltene | |
| es | Anomalía rara de la refracción | |
| it | Anomalia rara della rifrazione | |
| nl | Zeldzame refractieanomalie | |
| pt | Anomalia refrativa, rara | |
| pl | Rzadka wada refrakcji | |
| cs | Vzácné refrakční anomálie | |
| uk | Рідкісна аномалія рефракції | |
| zh | 罕见折光异常 | |
| tr | Nadir kırma kusuru anomalisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681677 | 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 (2):
- ORPHA:101435Rare genetic eye disease
rare genetic diseases - ORPHA:97966Rare ophthalmic disorder
rare ophthalmic disorders
Codes that Orphanet moved or referred to this one:
- ORPHA:98620OBSOLETE: Syndromic myopia referred to · inactive
- ORPHA:183601OBSOLETE: Rare genetic refraction anomaly 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98618
- This record as JSON: /data/d/98618.json