ORPHA:98668
Vitreoretinopathy
- 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 | Vitreoretinopathy | |
| fr | Vitréorétinopathie | |
| de | Vitreoretinopathie | |
| es | Vitreorretinopatía | |
| it | Vitreoretinopatia | |
| nl | Vitreoretinopathie | |
| pt | Vitreorretinopatia | |
| pl | Witreoretinopatia | |
| cs | Vitreoretinopatie | |
| uk | Вітреоретинопатія | |
| zh | 玻璃体视网膜病变 | |
| tr | Vitreoretinopati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C0344290 | 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 (2):
- ORPHA:522572Rare genetic retinal disorder
rare genetic diseases - ORPHA:519315Rare retinal disorder
rare ophthalmic disorders
Codes that Orphanet moved or referred to this one:
- ORPHA:98669OBSOLETE: Congenital vitreoretinal dysplasia referred to · inactive
- ORPHA:98670OBSOLETE: Vitreoretinal degeneration referred to · inactive
- ORPHA:519304OBSOLETE: Isolated vitreoretinopathy referred to · inactive
- ORPHA:519327OBSOLETE: Syndromic vitreoretinopathy 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/98668
- This record as JSON: /data/d/98668.json