ORPHA:674947
Diffuse unilateral subacute neuroretinitis
Synonyms: DUSN · Unilateral wipe-out syndrome
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Diffuse unilateral subacute neuroretinitis | DUSN · Unilateral wipe-out syndrome |
| fr | Neurorétinite subaiguë unilatérale diffuse | NSDU |
| de | Diffuse unilaterale subakute Neuroretinitis | DUSN · Unilaterales Wipe-out-Syndrom |
| es | Neurorretinitis subaguda unilateral difusa | DUSN · NSUD · Síndrome de pérdida de visión unilateral |
| it | Neuroretinite subacuta monolaterale diffusa | DUSN · Sindrome da wipe-out monolaterale |
| nl | Diffuse unilaterale subacute neuroretinitis | DUSN · Unilaterale 'wipe-out'-syndroom |
| pt | Neuroretinite subaguda unilateral difusa | DUSN · Síndrome wipe-out unilateral |
| pl | Rozlane jednostronne podostre zapalenie nerwu wzrokowego i siatkówki | = en |
| cs | Difuzní jednostranná subakutní neuroretinitida | = en |
| uk | Дифузний односторонній підгострий нейроретиніт | DUSN · Синдром одностороннього винищення |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | H30.1 | NTBT | attributed | validated |
| ICD-11 | 9B65.0 | NTBT | index | validated |
| MONDO | 0971127 | E | validated | |
| MONDO | 971127 | E | validated | |
| UMLS | C0339404 | 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 (3):
- ORPHA:730376Rare acquired isolated progressive generalized retinal disorder
rare ophthalmic disorders - ORPHA:519351Rare optic nerve disorder
rare ophthalmic disorders - ORPHA:163588Rare parasitic disease
rare infectious diseases
No children.
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/674947
- This record as JSON: /data/d/674947.json