ORPHA:716195
Rare inflammatory choroidal disorder
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare inflammatory choroidal disorder | |
| fr | Maladie inflammatoire choroïdienne rare | |
| de | Seltene entzündliche Störung der Choroidea | |
| es | Trastorno coroideo inflamatorio raro | |
| it | Malattia infiammatoria rara della coroide | |
| nl | Zeldzame inflammatoire aandoening van choroidea | Zeldzame inflammatoire aandoening van vaatvlies · Zeldzame inflammatoire choroïdale aandoening |
| pt | Rare inflammatory choroidal disorder | |
| pl | Rzadkie zapalne zaburzenie naczyniówki | |
| cs | Rare inflammatory choroidal disorder |
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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 (1):
- ORPHA:519309Rare choroidal disorder
rare ophthalmic disorders
Children (7):
- ORPHA:714164Acute posterior multifocal placoid pigment epitheliopathy
- ORPHA:179Birdshot chorioretinopathy
- ORPHA:714154Idiopathic multifocal choroiditis
- ORPHA:714160Presumed ocular histoplasmosis syndrome
- ORPHA:580951Punctate inner choroidopathy
- ORPHA:35686Serpiginous choroiditis
- ORPHA:3437Vogt-Koyanagi-Harada disease
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/716195
- This record as JSON: /data/d/716195.json