Infectious panuveitis
- Type
- Disease
- Group
- Disorder
- Age of onset
- All ages
- Status
- active
A rare ophthalmic disorder characterized by generalized inflammation of all parts of the uveal tract (iris, ciliary body, and choroid), simultaneously involving adjacent vitreous and retina, without any predominant site of inflammation, due to viral, bacterial, fungal, or parasitic infections. Clinical symptoms include pain, photophobia, redness, blurring of vision, and floaters. Signs on examination are lid edema, ciliary injection, chemosis, keratic precipitates, cells in the anterior chamber, hypopyon, iris nodules and neovascularization, posterior synechiae, macular edema, vitreous and retinal hemorrhage, and retinal detachment, among others. Complications may result in visual loss.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Infectious panuveitis | |
| fr | Panuvéite infectieuse | |
| de | Panuveitis, infektiöse | |
| es | Panuveítis infecciosa | |
| it | Panuveite infettiva | |
| nl | Infectieuze panuveïtis | |
| pt | Panuveíte infeciosa | |
| pl | Zakaźne zapalenie wszystkich struktur błony naczyniowej oka | |
| cs | Infekční panuveitida | |
| uk | Інфекційний панувеїт | |
| zh | 感染性全葡萄膜炎 | |
| tr | Bulaşıcı panüveit |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | H44.1 | NTBT | attributed | validated |
| ICD-11 | 9C20.1 | E | specific | validated |
| MONDO | 0017211 | E | validated | |
| UMLS | C5230354 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:280898Panuveitis
rare ophthalmic disorders
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-9 / 100 000 | 4.4 / 100 000 | United States | Value and class | Validated | 32841267[PMID] |
| 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.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/279925
- This record as JSON: /data/d/279925.json