ORPHA:519270
Rare disorder with entropion
- 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 entropion | |
| fr | Maladie rare avec entropion | |
| de | Seltene Erkrankung mit Entropium | |
| es | Trastorno raro con entropión | |
| it | Malattia rara con entropion | |
| nl | Zeldzame aandoening met entropion | |
| pt | Doença rara com entropion | |
| pl | Choroba rzadka z wywinięciem do wewnątrz (entropion) powieki | |
| cs | Vzácná porucha s entropiem | |
| uk | Рідкісний розлад з ентропіоном | |
| zh | 罕见的眼睑内翻障碍 | |
| tr | Entropiyon ileseyreden nadir hastalık |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681385 | 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:98567Rare eyelid malposition disorder
rare developmental anomalies during embryogenesis; rare ophthalmic disorders
Codes that Orphanet moved or referred to this one:
- ORPHA:98568OBSOLETE: Congenital entropion referred to · inactive
- ORPHA:98569OBSOLETE: Secondary entropion referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
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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/519270
- This record as JSON: /data/d/519270.json