idiopathic uveal effusion syndrome
MONDO:0016206Mondo
Findings
No curated finding names idiopathic uveal effusion syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
13 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.
- Abnormal sclera morphologyHPOHP:0000591
- Very frequent (80% to 99% of cases)
- Abnormal anterior eye segment morphologyHPOHP:0004328
- Frequent (30% to 79% of cases)
- Increased CSF protein concentrationHPOHP:0002922
- Frequent (30% to 79% of cases)
- Reduced visual acuityHPOHP:0007663
- Frequent (30% to 79% of cases)
- Scleral thickeningHPOHP:0030823
- Frequent (30% to 79% of cases)
- Serous retinal detachmentHPOHP:0012231
- Frequent (30% to 79% of cases)
- Subretinal fluidHPOHP:0031526
- Frequent (30% to 79% of cases)
- Superficial episcleral hyperemiaHPOHP:0025339
- Frequent (30% to 79% of cases)
- Blurred visionHPOHP:0000622
- Occasional (5% to 29% of cases)
- MetamorphopsiaHPOHP:0012508
- Occasional (5% to 29% of cases)
- MicrophthalmiaHPOHP:0000568
- Occasional (5% to 29% of cases)
- Retinal foldHPOHP:0008052
- Occasional (5% to 29% of cases)
Reported absent (1)
- Abnormal intraocular pressureHPOHP:0012632
Show the remaining 1
- Visual field defectHPOHP:0001123
- Occasional (5% to 29% of cases)
Where it sits
- A kind of