ORPHA:183601
OBSOLETE: Rare genetic refraction anomaly
inactive · referred to ORPHA:98618Rare refraction anomaly
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare refraction anomaly
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Rare genetic refraction anomaly | |
| fr | OBSOLETE : Anomalie génétique rare de la réfraction | |
| de | OBSOLET: Refraktionsanomalie, genetisch bedingte, seltene | |
| es | OBSOLETO: Anomalía genética rara de refracción | |
| it | OBSOLETO: Anomalia genetica rara della rifrazione | |
| nl | OBSOLEET: Zeldzame genetische refractieanomalie | |
| pt | OBSOLETO: Anomalia de refração genética rara | |
| pl | NIEAKTUALNE: Rzadka genetyczna wada refrakcji | |
| cs | NEAKTUÁLNÍ: Vzácné dědičné refrakční anomálie | |
| uk | ЗАСТАРІЛО: Рідкісна генетично обумовлена аномалія рефракції | |
| zh | 弃用：罕见遗传性折射异常 | |
| tr | Eski adı: Nadir genetik kırılma anomalisi |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/183601
- This record as JSON: /data/d/183601.json