ORPHA:522556
Rare genetic corneal 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 genetic corneal disorder | |
| fr | Maladie génétique cornéenne rare | |
| de | Seltene genetische Erkrankung der Kornea | |
| es | Trastorno corneal genético raro | |
| it | Malattia genetica rara corneale | |
| nl | Zeldzame genetische aandoening van cornea | Zeldzame genetische aandoening van hoornvlies |
| pt | Doença da córnea genética rara | |
| pl | Rzadka choroba rogówki uwarunkowana genetycznie | |
| cs | Vzácná genetická porucha rohovky | |
| uk | Рідкісне генетично обумовлене захворювання рогівки | |
| zh | 罕见遗传性角膜病 | |
| tr | Nadir genetik kornea bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681415 | 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:522538Rare genetic disorder of the anterior segment of the eye
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/522556
- This record as JSON: /data/d/522556.json