exudative vitreoretinopathy 7
MONDO:0033123Mondo
Findings
No curated finding names exudative vitreoretinopathy 7 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
- Juvenile onset
HPO, annotations 2026-09-02
Features
6 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.
- Exudative vitreoretinopathyHPOHP:0030490
- NystagmusHPOHP:0000639
- Retinal degenerationHPOHP:0000546
- Retinal detachmentHPOHP:0000541
- Retinal foldHPOHP:0008052
- Retinal holeHPOHP:0011530
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.
- CTNNB1HGNC:2514
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- Moderate · Ambry Genetics · Autosomal dominant · 2018