ORPHA:522526
Rare genetic 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 genetic palpebral disorder | |
| fr | Maladie génétique rare de la paupière | |
| de | Seltene genetische Krankheit des Augenlids | |
| es | Trastorno palpebral genético raro | |
| it | Malattia genetica rara della palpebra | |
| nl | Zeldzame genetische palpebrale aandoening | Zeldzame genetische aandoening van ooglid |
| pt | Doença palpebral genética rara | |
| pl | Rzadka choroba powiek uwarunkowana genetycznie | |
| cs | Vzácná genetická palpebrální porucha | |
| uk | Рідкісне генетично обумовлене пальпебральне захворювання | |
| zh | 罕见遗传性眼睑疾病 | |
| tr | Nadir genetik palpebral bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681426 | 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:183557Genetic developmental defect of the eye
rare genetic diseases - ORPHA:522524Rare genetic disorder of the ocular adnexa
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/522526
- This record as JSON: /data/d/522526.json