ORPHA:482092
Rare idiopathic macular telangiectasia
- 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 idiopathic macular telangiectasia | |
| fr | Télangiectasie maculaire idiopathique rare | |
| de | Seltene idiopathische makuläre Teleangiektasie | |
| es | Telangiectasia macular idiopática rara | |
| it | Telangectasia maculare idiopatica rara | |
| nl | Zeldzame idiopathische maculaire teleangiëctasie | |
| pt | Telangiectasia macular idiopática rara | |
| pl | Rzadka idiopatyczna teleangiektazja w plamce | |
| cs | Vzácná idiopatická makulární teleangiektázie | |
| uk | Рідкісна ідіопатична макулярна телеангіектазія | |
| zh | 罕见的特发性黄斑毛细血管扩张 | |
| tr | Nadir görülen idiyopatik maküler telenjiektazi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18833 | E | validated | |
| UMLS | C5681247 | 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 (3):
- ORPHA:71281Rare central nervous system and retinal vascular disease
rare neurological diseases - ORPHA:716432Rare isolated progressive predominantly macular disorder
rare ophthalmic disorders - ORPHA:716466Rare isolated progressive retinal vasculopathy
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/482092
- This record as JSON: /data/d/482092.json