LRP5-related exudative vitreoretinopathy
MONDO:0700228Mondo
Findings
No curated finding names LRP5-related exudative vitreoretinopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any exudative vitreoretinopathy with or without osteoporosis caused by variants in the LRP5 gene.
Definition from the Mondo Disease Ontology (MONDO:0700228), read 2026-09-29. CC BY 4.0.
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.
- LRP5HGNC:6697
- Definitive · ClinGen · Autosomal recessive · 2023
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Strong · PanelApp Australia · Autosomal recessive · 2025
Where it sits
- A kind of
- Narrower terms (2)
Other names
1 name
Resolves to: LRP5-related exudative vitreoretinopathy
- Also called
- LRP5-related exudative vitreoretinopathy with or without osteoporosis