ORPHA:519313
Rare macular 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare macular disorder | |
| fr | Maladie maculaire rare | |
| de | Seltene Krankheit der Makula | |
| es | Trastorno macular raro | |
| it | Patologia maculare rara | |
| nl | Zeldzame aandoening van macula | Zeldzame aandoening van gele vlek |
| pt | Doença macular rara | |
| pl | Rzadka choroba plamki żółtej | |
| cs | Vzácná porucha makuly | |
| uk | Рідкісний макулярний розлад | |
| zh | 罕见黄斑病变 | |
| tr | Nadir maküler bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681379 | 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
Codes that Orphanet moved or referred to this one:
- ORPHA:519302OBSOLETE: Isolated macular dystrophy referred to · inactive
- ORPHA:519323OBSOLETE: Syndromic macular 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/519313
- This record as JSON: /data/d/519313.json