ORPHA:520814
Rare disorder of the visual organs
- 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 of the visual organs | |
| fr | Maladie rare des organes visuels | |
| de | Seltene Krankheit des Sehorgans | |
| es | Trastorno raro de los órganos visuales | |
| it | Malattia rara dell'organo della vista | |
| nl | Zeldzame aandoening van visuele organen | |
| pt | Doença rara dos orgãos visuais | |
| pl | Rzadka choroba narządu wzroku | |
| cs | Vzácná porucha zrakových orgánů | |
| uk | Рідкісне захворювання органів зору | |
| zh | 罕见的视觉器官病变 | |
| tr | Görme organlarında görülen nadir bozukluk |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681453 | 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:97966Rare ophthalmic disorder
rare ophthalmic disorders
Children (8):
- ORPHA:140653Neuro-ophthalmological disease
- ORPHA:519329Rare disorder involving multiple structures of the eye
- ORPHA:519284Rare disorder of the anterior segment of the eye
- ORPHA:519266Rare disorder of the ocular adnexa
- ORPHA:519311Rare disorder of the posterior segment of the eye
- ORPHA:519298Rare scleral disorder
- ORPHA:519272Structural developmental eye defect
- ORPHA:98715Uveitis
Codes that Orphanet moved or referred to this one:
- ORPHA:98702OBSOLETE: Connective tissue disease with eye involvement referred to · inactive
- ORPHA:98709OBSOLETE: Ectodermal malformation syndrome associated with ocular features referred to · inactive
4
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/520814
- This record as JSON: /data/d/520814.json