ORPHA:714164
Acute posterior multifocal placoid pigment epitheliopathy
Synonyms: APMPPE
- Type
- Disease
- Group
- Disorder
- 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 | Acute posterior multifocal placoid pigment epitheliopathy | APMPPE |
| fr | Epithéliopathie en plaque | EPP |
| de | Akute posteriore multifokale plakoide Pigmentepitheliopathie | = en |
| es | Epiteliopatía pigmentaria placoide multifocal posterior aguda | = en |
| it | Epiteliopatia multifocale posteriore acuta a placche pigmentate | = en |
| nl | Acute multifocale placoïde pigmentepitheliopathie | = en |
| pt | Acute posterior multifocal placoid pigment epitheliopathy | |
| pl | Ostra tylna wieloogniskowa plackowata epiteliopatia barwnikowa | = en |
| cs | Acute posterior multifocal placoid pigment epitheliopathy | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:90061Non-infectious posterior uveitis
rare ophthalmic disorders - ORPHA:716195Rare inflammatory choroidal disorder
rare ophthalmic disorders
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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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/714164
- This record as JSON: /data/d/714164.json