exudative vitreoretinopathy 1
MONDO:0007589Mondo
Findings
No curated finding names exudative vitreoretinopathy 1 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Adult onset · Infantile onset · Slowly progressive
HPO, annotations 2026-09-02
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.
- Avascular peripheral retinaHPOHP:0007685
- 14 of 14 reported patients
- Reduced visual acuityHPOHP:0007663
- 12 of 14 reported patients
- Vitreous floatersHPOHP:0100832
- 8 of 12 reported patients
- EsotropiaHPOHP:0000565
- 1 of 2 reported patients
- Exudative vitreoretinopathyHPOHP:0030490
- 1 of 2 reported patients
- Retinal detachmentHPOHP:0000541
- 6 of 16 reported patients
- Ectopic foveaHPOHP:0025007
- 4 of 12 reported patients
- Falciform retinal foldHPOHP:0001493
- 4 of 12 reported patients
- Retinal holeHPOHP:0011530
- 4 of 14 reported patients
- Retinal exudateHPOHP:0001147
- 3 of 12 reported patients
- Retinal neovascularizationHPOHP:0030666
- 0 of 2 reported patients
- Subcapsular cataractHPOHP:0000523
Show the remaining 1
- Vitreous hemorrhageHPOHP:0007902
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- FZD4HGNC:4042
- Definitive · Ambry Genetics · Semidominant · 2024
- Definitive · G2P · Autosomal dominant · 2017
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2022
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2022
Where it sits
Other names
1 name
Resolves to: exudative vitreoretinopathy 1
- Also called
- exudative vitreoretinopathy type 1