Trait
Vitreoretinopathy
Ocular abnormality characterized by premature degeneration of the vitreous and the retina that may be associated with increased risk of retinal detachment.
Summary
- Also called
- Vitreoretinal abnormality, Vitreoretinal degeneration
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
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Get my Genome Test18 genes linked to Vitreoretinopathy
Changes in these genes cause rare conditions in which Vitreoretinopathy is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| COL2A1collagen type II alpha 1 chain | Always | In 3 conditions |
| COL9A2collagen type IX alpha 2 chain | Always | In 2 conditions |
| CTNNB1catenin beta 1 | Always | In 1 condition |
| FZD4frizzled class receptor 4 | Always | In 1 condition |
| LRP5LDL receptor related protein 5 | Always | In 2 conditions |
| NDPnorrin cystine knot growth factor NDP | Always | In 1 condition |
| PAK2p21 (RAC1) activated kinase 2 | Always | In 2 conditions |
| TSPAN12tetraspanin 12 | Always | In 1 condition |
| ZNF408zinc finger protein 408 | Always | In 1 condition |
| COL18A1collagen type XVIII alpha 1 chain | Very often (80–99%) | In 2 conditions |
| COL11A1collagen type XI alpha 1 chain | Often (30–79%) | In 2 conditions |
| COL9A1collagen type IX alpha 1 chain | Often (30–79%) | In 1 condition |
| COL9A3collagen type IX alpha 3 chain | Often (30–79%) | In 1 condition |
| LOXL3lysyl oxidase like 3 | Often (30–79%) | In 1 condition |
| CAPN5calpain 5 | Not recorded | In 1 condition |
| CRB1crumbs cell polarity complex component 1 | Not recorded | In 1 condition |
| NR2E3nuclear receptor subfamily 2 group E member 3 | Not recorded | In 1 condition |
| VCANversican | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
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Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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