Idiopathic posterior uveitis
- Type
- Disease
- Group
- Disorder
- Status
- active
Idiopathic posterior uveitis is a rare, potentially sight-threatening, ocular disease, not attributed to any specific ocular or systemic cause, characterized by focal, multifocal or diffuse non-infectious inflammation in the posterior uvea (i.e. choroiditis, chorioretinitis, retinitis and neuroretinitis). Visual morbidity due to complications (including cystoid macular edema and choroidal neovascularization) has been reported.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Idiopathic posterior uveitis | |
| fr | Uvéite postérieure idiopathique | |
| de | Uveitis, posteriore, idiopathische | |
| es | Uveítis posterior idiopática | |
| it | Uveite posteriore idiopatica | |
| nl | Idiopathische posterieure uveïtis | |
| pt | Uveíte posterior idiopática | |
| pl | Idiopatyczne zapalenie tylnego odcinka błony naczyniowej | |
| cs | Idiopatická zadní uveitida | |
| uk | Ідіопатичний задній увеїт | |
| zh | 特发性后葡萄膜炎 | |
| tr | İdiyopatik posterior üveit |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | H30.9 | NTBT | attributed | validated |
| ICD-11 | 9B65.0 | NTBT | attributed | validated |
| MONDO | 0017257 | E | validated | |
| UMLS | C4751435 | 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:90061Non-infectious posterior uveitis
rare ophthalmic disorders
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/280917
- This record as JSON: /data/d/280917.json