ORPHA:98570
Congenital ectropion
- 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 ectropion | |
| fr | Ectropion congénital | |
| de | Ektropium, kongenitales | |
| es | Ectropión congénita | |
| it | Ectropion congenito | |
| nl | Congenitaal ectropion | |
| pt | Ectropion congénito | |
| pl | Wrodzone wywinięcie powiek - ektropion | |
| cs | Vrozená ektropia | |
| uk | Вроджений ектропіон | |
| zh | 先天性眼睑外翻 | |
| tr | Doğumsal ektropiyon |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q10.1 | E | specific | validated |
| ICD-11 | LA14.03 | E | specific | validated |
| MONDO | 0020161 | E | validated | |
| UMLS | C0266578 | 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 (1):
- ORPHA:519268Rare disorder with ectropion
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.
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/98570
- This record as JSON: /data/d/98570.json