ORPHA:98561
Congenital malformation of the eyelid
- 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 | Congenital malformation of the eyelid | |
| fr | Malformation congénitale de la paupière | |
| de | Augenlid-Fehlbildung | |
| es | Malformación de los párpados | |
| it | Malformazione delle palpebre | |
| nl | Ooglidmalformatie | |
| pt | Malformação da pálpebra | |
| pl | Wady powiek | |
| cs | Malformace očních víček | |
| uk | Вроджена вада розвитку повік | |
| zh | 眼睑先天畸形 | |
| tr | Doğumsal göz kapağı malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C0266572 | E | validated | |
| MedDRA | 10061146 | 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:522526Rare genetic palpebral disorder
rare genetic diseases - ORPHA:98560Rare palpebral disorder
rare developmental anomalies during embryogenesis; 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/98561
- This record as JSON: /data/d/98561.json