ORPHA:715855
Acute exudative polymorphous vitelliform maculopathy
Synonyms: AEPVM
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acute exudative polymorphous vitelliform maculopathy | AEPVM |
| fr | Maculopathie vitelliforme polymorphe exsudative aiguë | MVPEA |
| de | Akute exsudative polymorphe vitelliforme Makulopathie | = en |
| es | Maculopatía viteliforme polimorfa exudativa aguda | = en |
| it | Maculopatia vitelliforme polimorfa essudativa acuta | MVPEA |
| nl | Acute exsudatieve polymorfe vitelliforme maculopathie | = en |
| pt | Acute exudative polymorphous vitelliform maculopathy | |
| pl | Ostra wysiękowa polimorficzna żółtkowata makulopatia | = en |
| cs | Acute exudative polymorphous vitelliform maculopathy | = en |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:716432Rare isolated progressive predominantly macular disorder
rare ophthalmic disorders
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 40 cases | Worldwide | Case(s) | Validated | ORPHANET | |
| Point prevalence | <1 / 1 000 000 | — | 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.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/715855
- This record as JSON: /data/d/715855.json