ORPHA:98681
Rare disorder with strabismus
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare disorder with strabismus | |
| fr | Maladie rare avec strabisme | |
| de | Strabismus mit Restriktionssyndrom, selten | |
| es | Estrabismo raro con síndrome de restricción | |
| it | Strabismo con una sindrome restrittiva rara | |
| nl | Zeldzaam strabisme- en restrictiesyndroom | |
| pt | Estrabismo e síndrome de restrição, raros | |
| pl | Rzadkie odmiany zeza i zespół restrykcyjny | |
| cs | Vzácné typy strabismu a restrikční syndromy | |
| uk | Рідкісний розлад з косоокістю | |
| zh | 罕见斜视障碍 | |
| tr | Şaşılık ile seyreden nadir bozukluk |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681695 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:519355Rare ocular motility/alignment disorder
rare ophthalmic disorders
Children (1):
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/98681
- This record as JSON: /data/d/98681.json