ORPHA:98575
Syndromic telecanthus
- 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 telecanthus | |
| fr | Télécanthus syndromique | |
| de | Telekanthus | |
| es | Telecanto | |
| it | Telecanto | |
| nl | Telecanthus | |
| pt | Telecanto | |
| pl | Telekantus | |
| cs | Telekanty | |
| uk | Синдромний телекант | |
| zh | 综合征型内眦距过宽 | |
| tr | Sendromik telekantus |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 8537 | E | validated | |
| UMLS | C0423113 | 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 (2):
- ORPHA:98567Rare eyelid malposition disorder
rare developmental anomalies during embryogenesis; rare ophthalmic disorders - ORPHA:522528Rare genetic eyelid malposition disorder
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98575
- This record as JSON: /data/d/98575.json