ORPHA:519317
Rare retinal vasculopathy
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare retinal vasculopathy | |
| fr | Vasculopathie rétinienne rare | |
| de | Seltene retinale Vaskulopathie | |
| es | Vasculopatía retiniana rara | |
| it | Vasculopatia retinica rara | |
| nl | Zeldzame retinale vasculopathie | |
| pt | Vasculopatia retiniana rara | |
| pl | Rzadka waskulopatia siatkówki | |
| cs | Vzácná vaskulopatie sítnice | |
| uk | Рідкісна васкулопатія сітківки | |
| zh | 罕见视网膜血管病变 | |
| tr | Nadir retinal vaskülopati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681376 | 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:519315Rare retinal disorder
rare ophthalmic disorders
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/519317
- This record as JSON: /data/d/519317.json