ORPHA:98560
Rare palpebral 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 palpebral disorder | |
| fr | Maladie rare de la paupière | |
| de | Palpebraler Defekt, seltener | |
| es | Enfermedad rara de los párpados | |
| it | Malattia rara delle palpebre | |
| nl | Zeldzame palpebrale ziekte | |
| pt | Doença palpebral, rara | |
| pl | Rzadka choroba powiek | |
| cs | Vzácná onemocnění víček | |
| uk | Рідкісне захворювання повік | |
| zh | 罕见眼睑障碍 | |
| tr | Nadir görülen palpebral bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681654 | 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:98553Developmental defect of the eye
rare developmental anomalies during embryogenesis - ORPHA:519266Rare disorder of the ocular adnexa
rare ophthalmic disorders
Codes that Orphanet moved or referred to this one:
- ORPHA:98572OBSOLETE: Canthal anomaly referred to · inactive
- ORPHA:98577OBSOLETE: Kinetic eyelid anomaly referred to · inactive
- ORPHA:98579OBSOLETE: Congenital upper palpebral retraction 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/98560
- This record as JSON: /data/d/98560.json