ORPHA:98564
Eyelid border 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Eyelid border anomaly | |
| fr | Anomalie du bord libre de la paupière | |
| de | Augenlidkante, Anomalie der | |
| es | Anomalía de los bordes de los párpados | |
| it | Anomalia del bordo palpebrale | |
| nl | Ooglidrandanomalie | |
| pt | Anomalia do bordo palpebrar | |
| pl | Anomalia brzegów powiek | |
| cs | Anomálie okrajů očního víčka | |
| uk | Аномалія краю повік | |
| zh | 眼睑边缘异常 | |
| tr | Göz kapağı kenar anomalisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681655 | 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 (1):
- ORPHA:98561Congenital malformation of the eyelid
rare developmental anomalies during embryogenesis; 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.
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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/98564
- This record as JSON: /data/d/98564.json