ORPHA:98623
Syndromic keratoconus
- 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 | Syndromic keratoconus | |
| fr | Syndromes comprenant un kératocône | |
| de | Keratokonus, syndromaler | |
| es | Queratocono sindrómico | |
| it | Cheratocono sindromico | |
| nl | Syndromale keratoconus | |
| pt | Queratocone sindromático | |
| pl | Syndromiczny stożek rogówki | |
| cs | Syndromy s keratokonem | |
| uk | Синдромальний кератоконус | |
| zh | 综合征性圆锥角膜 | |
| tr | Sendromik keratokonus |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681674 | 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:519288Rare disorder with corneal involvement as a major feature
rare ophthalmic disorders
Codes that Orphanet moved or referred to this one:
- ORPHA:156071OBSOLETE: Keratoconus 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/98623
- This record as JSON: /data/d/98623.json