Trait
Serous retinal detachment
A type of retinal detachment such that fluid is present in the subretinal space and separate the neurosensory retina from the retinal pigment epithelium. It is not associated with a full-thickness break nor a tractional component. Due to breakdown of outer blood-retina barrier or increased exudation from abnormal vasculature or defective outflow.
Summary
- Also called
- Exudative retinal detachment, Non-rhegmatogenous retinal detachment
- Body system
- Abnormality of the eye
Read the genes linked to Serous retinal detachment, and the rest of your genome, with one test.
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Get my Genome Test13 genes linked to Serous retinal detachment
Changes in these genes cause rare conditions in which Serous retinal detachment 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 |
|---|---|---|
| TINF2TERF1 interacting nuclear factor 2 | Always | In 3 conditions |
| LRP5LDL receptor related protein 5 | Often (30–79%) | In 2 conditions |
| MAXMYC associated transcriptional regulator X | Often (30–79%) | In 1 condition |
| CFHcomplement factor H | Sometimes (5–29%) | In 1 condition |
| CFIcomplement factor I | Sometimes (5–29%) | In 1 condition |
| DNMT3BDNA methyltransferase 3 beta | Sometimes (5–29%) | In 1 condition |
| DUX4double homeobox 4 | Sometimes (5–29%) | In 1 condition |
| DUX4L1double homeobox 4 like 1 (pseudogene) | Sometimes (5–29%) | In 1 condition |
| EFEMP1EGF-like fibulin extracellular matrix protein 1 | Sometimes (5–29%) | In 1 condition |
| FRG1FSHD region gene 1 | Sometimes (5–29%) | In 2 conditions |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Sometimes (5–29%) | In 1 condition |
| CTC1CST telomere replication complex component 1 | Not recorded | In 1 condition |
| IGFBP7insulin like growth factor binding protein 7 | 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.
Broader traits
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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