ORPHA:98571
Secondary 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 | Secondary ectropion | |
| fr | Ectropion secondaire | |
| de | Ektropium, sekundäres | |
| es | Ectropión secundario | |
| it | Ectropion secondario | |
| nl | Secundair ectropion | |
| pt | Ectropion secundário | |
| pl | Wtórne wywinięcie powiek - ektropion | |
| cs | Sekundární ektropia | |
| uk | Вторинний ектропіон | |
| zh | 继发性眼睑外翻 | |
| tr | Sekonder ektropiyon |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | H02.1 | E | specific | validated |
| UMLS | C5681652 | 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
Children (8):
- ORPHA:281097Autosomal recessive congenital ichthyosis
- ORPHA:1231Barber-Say syndrome
- ORPHA:870Down syndrome
- ORPHA:2269Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome
- ORPHA:246Postaxial acrofacial dysostosis
- ORPHA:910Xeroderma pigmentosum
- ORPHA:90342Xeroderma pigmentosum variant
- ORPHA:220295Xeroderma pigmentosum-Cockayne syndrome complex
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/98571
- This record as JSON: /data/d/98571.json