ORPHA:522550
Lens size anomaly of genetic origin
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Lens size anomaly of genetic origin | |
| fr | Anomalie de taille du cristallin d'origine génétique | |
| de | Genetisch bedingte Größenanomalie der Linse | |
| es | Anomalía del tamaño de la lente de origen genético | |
| it | Anomalia della dimensione della lente di origine genetica | |
| nl | Anomalie van omvang van lens van genetische oorsprong | |
| pt | Cristalino com dimensão anómala de origem genética | |
| pl | Wady wielkości soczewek oka uwarunkowane genetycznie | |
| cs | Geneticky podmíněná anomálie velikosti čočky | |
| uk | Генетично обумовлена аномалія розміру кришталика | |
| zh | 遗传性晶状体大小异常 | |
| tr | Genetik kökenli lens boyutu anomalisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681414 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:183557Genetic developmental defect of the eye
rare genetic diseases - ORPHA:183607Genetic lens and zonula anomaly
rare genetic diseases
Children (1):
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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/522550
- This record as JSON: /data/d/522550.json