Trait
Retinal flecks
Presence of multiple yellowish-white lesions of various size and configuration on the retina not related to vascular lesions.
Summary
- Body system
- Abnormality of the eye
This page as data
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Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Alport SyndromeReads 3 of these genesCOL4A3COL4A4COL4A5About this report →
- Hereditary Macular DystrophiesReads 4 of these genesBEST1PRPH2RDH5RLBP1About this report →
- Stargardt DiseaseReads 2 of these genesABCA4PROM1About this report →
- Congenital Stationary Night BlindnessReads 4 of these genesPRPH2RDH5RHORLBP1About this report →
Show 4 more reports
- Retinitis PigmentosaReads 7 of these genesABCA4BEST1PROM1PRPH2RDH5RHOAbout this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 2 of these genesRPGRIP1PRPH2About this report →
- VitreoretinopathyReads 1 of these genesBEST1About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesZFYVE26About this report →
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Get my Genome Test15 genes linked to Retinal flecks
Changes in these genes cause rare conditions in which Retinal flecks 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 |
|---|---|---|
| PLA2G5phospholipase A2 group V | Always | In 1 condition |
| RDH8retinol dehydrogenase 8 | Always | In 1 condition |
| RPGRIP1RPGR interacting protein 1 | Always | In 1 condition |
| UBAP1Lubiquitin associated protein 1 like | Always | In 1 condition |
| ZFYVE26zinc finger FYVE-type containing 26 | Often (30–79%) | In 1 condition |
| COL4A3collagen type IV alpha 3 chain | Sometimes (5–29%) | In 1 condition |
| COL4A4collagen type IV alpha 4 chain | Sometimes (5–29%) | In 1 condition |
| COL4A5collagen type IV alpha 5 chain | Sometimes (5–29%) | In 1 condition |
| ABCA4ATP binding cassette subfamily A member 4 | Not recorded | In 1 condition |
| BEST1bestrophin 1 | Not recorded | In 2 conditions |
| PROM1prominin 1 | Not recorded | In 1 condition |
| PRPH2peripherin 2 | Not recorded | In 1 condition |
| RDH5retinol dehydrogenase 5 | Not recorded | In 1 condition |
| RHOrhodopsin | Not recorded | In 1 condition |
| RLBP1retinaldehyde binding protein 1 | 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 2026.10.17-8666dff2.
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