ORPHA:714150
Stellate non-hereditary idiopathic foveomacular retinoschisis
Synonyms: SNIFR
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Stellate non-hereditary idiopathic foveomacular retinoschisis | SNIFR |
| fr | Rétinoschisis fovéomaculaire idiopathique non héréditaire stellaire | |
| de | Sternförmige nicht-hereditäre idiopathische foveo-makuläre Retinoschisis | = en |
| es | Retinosquisis foveomacular estrellada idiopática no hereditaria | = en |
| it | Retinoschisi foveo-maculare stellata idiopatica non ereditaria | = en |
| nl | Stervormige niet-hereditaire idiopathische foveomaculaire retinoschisis | SNIFR · Stervormige niet-erfelijke idiopathische retinoschisis in macula en fovea |
| pt | Stellate non-hereditary idiopathic foveomacular retinoschisis | |
| pl | Gwiaździste, niedziedziczne, idiopatyczne dołkowo-plamkowe rozwarstwienie siatkówki | = en |
| cs | Stellate non-hereditary idiopathic foveomacular retinoschisis | = en |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | H33.5 | NTBT | attributed | 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:716432Rare isolated progressive predominantly macular disorder
rare ophthalmic disorders
No children.
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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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/714150
- This record as JSON: /data/d/714150.json