ORPHA:674953
Multiple evanescent white dot syndrome
Synonyms: MEWDS
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Multiple evanescent white dot syndrome | MEWDS |
| fr | Syndrome des taches blanches évanescentes et multiples | MEWDS · Syndrome des taches blanches du fond d'oeil |
| de | Syndrom der multiplen evaneszenten weißen Punkte | = en |
| es | Síndrome de múltiples puntos blancos evanescentes | MEWDS · SMPBE |
| it | Sindrome dei punti bianchi multipli evanescenti | = en |
| nl | 'Multiple evanescent white dot'-syndroom | = en |
| pt | Síndrome de múltiplos pontos brancos evanescentes | = en |
| pl | Zespół mnogiej zanikającej białej kropki | = en |
| cs | Syndrom vícečetných mizejících bílých skvrn | = en |
| uk | Синдром множинних зникаючих білих крапок | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | H30.8 | NTBT | attributed | validated |
| ICD-11 | 9B65.0 | NTBT | index | validated |
| MONDO | 0971128 | E | validated | |
| MONDO | 971128 | E | validated | |
| UMLS | C0730322 | 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:716296Rare isolated non-progressive predominantly chorioretinal disorder
rare ophthalmic disorders
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/674953
- This record as JSON: /data/d/674953.json