ORPHA:519268
Rare disorder with 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare disorder with ectropion | |
| fr | Maladie rare avec ectropion | |
| de | Seltene Erkrankung mit Ektropium | |
| es | Trastorno raro con ectropión | |
| it | Malattia rara con ectropion | |
| nl | Zeldzame aandoening met ectropion | |
| pt | Doença rara com ectropion | |
| pl | Choroba rzadka z wywinięciem na zewnątrz (ektropion) powieki | |
| cs | Vzácná porucha s ektropiem | |
| uk | Рідкісний розлад з ектропіоном | |
| zh | 罕见的眼睑外翻障碍 | |
| tr | Ektropiyon ile seyreden nadir hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681384 | 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:98567Rare eyelid malposition disorder
rare developmental anomalies during embryogenesis; rare ophthalmic disorders - ORPHA:522528Rare genetic eyelid malposition disorder
rare genetic diseases
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/519268
- This record as JSON: /data/d/519268.json