ORPHA:728633
Idiopathic orbital inflammation syndrome
Synonyms: Orbital pseudotumor · Orbital inflammatory pseudotumor · OIP · IOI syndrome · Syndrome IOI
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult, Childhood, Elderly
- 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 | Idiopathic orbital inflammation syndrome | Orbital pseudotumor · Orbital inflammatory pseudotumor · OIP · IOI syndrome · Syndrome IOI |
| fr | Syndrome d'inflammation de l'orbite idiopathique | Pseudotumeur inflammatoire orbitaire |
| de | Idiopathisches orbitales Entzündungssyndrom | Idiopathische Orbitaentzündung · IOE · IOI-Syndrom · Idiopathische entzündliche Orbitopathie |
| es | Síndrome de inflamación orbitaria idiopática | PIO · Pseudotumor inflamatorio orbitario · Pseudotumor orbitario · Síndrome IOI |
| it | Sindrome infiammatoria idiopatica dell'orbita | OIP · Sindrome IOI · Pseudotumore dell'orbita · Pseudotumore infiammatorio dell'orbita |
| nl | Idiopathische inflammatie van orbita | Inflammatoire pseudotumor van orbita · Pseudotumor van orbita · IOI-syndroom · OIP |
| pt | Idiopathic orbital inflammation syndrome | |
| pl | Idiopathic orbital inflammation syndrome | = en |
| cs | Idiopathic orbital inflammation syndrome | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:519329Rare disorder involving multiple structures of the eye
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/728633
- This record as JSON: /data/d/728633.json