ORPHA:522560
Genetic corneal dystrophy
- 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 | Genetic corneal dystrophy | |
| fr | Dystrophie cornéenne génétique | |
| de | Genetisch bedingte Hornhautdystrophie | |
| es | Distrofia corneal genética | |
| it | Distrofia corneale genetica | |
| nl | Genetische corneadystrofie | |
| pt | Distrofia da córnea genética | |
| pl | Dystrofia rogówki uwarunkowana genetycznie | |
| cs | Genetická dystrofie rohovky | |
| uk | Генетично обумовлена дистрофія рогівки | |
| zh | 遗传性角膜营养不良 | |
| tr | Genetik kornea distrofisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681409 | 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:522558Rare genetic disorder with corneal involvement as a major feature
rare genetic diseases
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/522560
- This record as JSON: /data/d/522560.json