ORPHA:522516
Rare genetic ocular motility/alignment 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 ocular motility/alignment disorder | |
| fr | Maladie génétique rare d'alignement ou de motilité oculaire | |
| de | Seltene genetische Störung der okulären Ausrichtung und Beweglichkeit | |
| es | Trastorno genético raro de la movilidad/alineamiento ocular | |
| it | Malattia genetica rara della motilità/allineamento oculare | |
| nl | Zeldzame genetische aandoening van beweging/stand van oog | |
| pt | Doença genética rara do alinhamento/mobilidade ocular | |
| pl | Rzadka choroba uwarunkowana genetycznie z zaburzeniami ruchomości gałki ocznej/nieprawidłowym ustawieniem gałek ocznych | |
| cs | Vzácná genetická porucha oční motility/postavení | |
| uk | Рідкісне генетично обумовлене порушення руху/вирівнювання очей | |
| zh | 罕见的遗传性眼球运动/对齐障碍 | |
| tr | Nadir genetik oküler hareketlilik/hizalanma bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681434 | 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:183616Genetic neuro-ophthalmological disease
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/522516
- This record as JSON: /data/d/522516.json