ORPHA:520820
Progressive external ophthalmoplegia
- 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 | Progressive external ophthalmoplegia | |
| fr | Ophtalmoplégie externe progressive | |
| de | Progressive externe Ophthalmoplegie | |
| es | Oftalmoplejía externa progresiva | |
| it | Oftalmoplegia esterna progressiva | |
| nl | Progressieve externe oftalmoplegie | |
| pt | Oftalmoplegia externa progressiva | |
| pl | Postępująca oftalmoplegia zewnętrzna | |
| cs | Progresivní zevní oftalmoplegie | |
| uk | Прогресуюча зовнішня офтальмоплегія | |
| zh | 进行性眼外肌麻痹 | |
| tr | ilerleyici eksternal oftalmopleji |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 9C82.0 | E | specific | validated |
| MONDO | 0005181 | E | validated | |
| MONDO | 5181 | E | validated | |
| GARD | 4503 | E | validated | |
| MedDRA | 10036802 | 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 (2):
- ORPHA:522522Rare genetic neuromuscular disorder with ocular motility/alignment anomaly
rare genetic diseases - ORPHA:519347Rare neuromuscular disorder with ocular motility/alignment anomaly
rare ophthalmic disorders
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/520820
- This record as JSON: /data/d/520820.json