idiopathic panuveitis
Findings
No curated finding names idiopathic panuveitis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Idiopathic panuveitis is a rare inflammatory eye disease, of unknown etiology, characterized by generalized inflammation of the uvea (iris, ciliary body, choroid), retina and vitreous with consequent ciliary spasm and posterior synechiae formation, leading to acute or chronic, unilateral or bilateral visual impairment and ocular discomfort or pain. Patients present an increased risk of development of cataracts, secondary glaucoma, cystoid macular edema and/or retinal detachment. It could potentially result in vision loss.
Definition from the Mondo Disease Ontology (MONDO:0017258), read 2026-09-29. CC BY 4.0.
Features
19 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Abnormality of visionHPOHP:0000504
- Frequent (30% to 79% of cases)
- Blurred visionHPOHP:0000622
- Frequent (30% to 79% of cases)
- Ocular painHPOHP:0200026
- Frequent (30% to 79% of cases)
- Red eyeHPOHP:0025337
- Frequent (30% to 79% of cases)
- Reduced visual acuityHPOHP:0007663
- Frequent (30% to 79% of cases)
- Vitreous hazeHPOHP:0030652
- Frequent (30% to 79% of cases)
- CataractHPO
Show the remaining 7
- Posterior synechiae of the anterior chamberHPOHP:0011484
- Occasional (5% to 29% of cases)
- Vitreous floatersHPOHP:0100832
- Occasional (5% to 29% of cases)
- Vitreous snowballsHPOHP:0030661
- Occasional (5% to 29% of cases)
- BlindnessHPOHP:0000618
- Very rare (1% to 4% of cases)
- Choroidal neovascularizationHPOHP:0011506
- Very rare (1% to 4% of cases)
- Epiretinal membraneHPOHP:0100014
- Very rare (1% to 4% of cases)
Where it sits
- A kind of
- Narrower terms (1)