ORPHA:519315
Rare retinal disorder
- 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 retinal disorder | |
| fr | Maladie rétinienne rare | |
| de | Seltene Krankheit der Retina | |
| es | Trastorno retiniano raro | |
| it | Patologia retinica rara | |
| nl | Zeldzame aandoening van retina | Zeldzame aandoening van netvlies |
| pt | Doença retiniana rara | |
| pl | Rzadka choroba siatkówki | |
| cs | Vzácná porucha sítnice | |
| uk | Рідкісне захворювання сітківки | |
| zh | 罕见视网膜病变 | |
| tr | Nadir retina bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681377 | 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:519311Rare disorder of the posterior segment of the eye
rare ophthalmic disorders
Codes that Orphanet moved or referred to this one:
- ORPHA:98657OBSOLETE: Genetic vitreous-retinal disease referred to · inactive
- ORPHA:98661OBSOLETE: Syndromic rod-cone dystrophy 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.
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/519315
- This record as JSON: /data/d/519315.json