Infectious anterior uveitis
- Type
- Disease
- Group
- Disorder
- Age of onset
- All ages
- Status
- active
A rare ophthalmic disorder characterized by inflammation primarily of the anterior part of the uvea (iris and ciliary body), due to an infectious etiology. Clinical symptoms are pain, redness, photophobia, and variable visual loss. Signs on examination include presence of inflammatory cells in the anterior chamber and anterior vitreous, keratic precipitates, hypopyon, iris nodules, posterior synechiae, and miosis, among others.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Infectious anterior uveitis | |
| fr | Uvéite antérieure infectieuse | |
| de | Uveitis, anteriore, infektiöse Form | |
| es | Uveítis anterior infecciosa | |
| it | Uveite anteriore infettiva | |
| nl | Infectieuze anterieure uveïtis | |
| pt | Uveíte anterior infeciosa | |
| pl | Zakaźne zapalenie przedniego odcinka błony naczyniowej oka | |
| cs | Infekční přední uveitida | |
| uk | Інфекційний передній увеїт | |
| zh | 感染性前葡萄膜炎 | |
| tr | Enfeksiyöz ön üveit |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | H20.0 | NTBT | attributed | validated |
| ICD-10 | H20.1 | NTBT | attributed | validated |
| ICD-10 | H20.2 | NTBT | attributed | validated |
| ICD-10 | H20.8 | NTBT | attributed | validated |
| ICD-10 | H20.9 | NTBT | attributed | validated |
| ICD-11 | 9A96.2 | E | specific | validated |
| MONDO | 0017210 | E | validated | |
| UMLS | C0154911 | 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:280886Anterior uveitis
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 | 1-5 / 10 000 | 27.7 / 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/279922
- This record as JSON: /data/d/279922.json