Trait
Moderate myopia
A moderate form of myopia with refractive error of between -3.00 and -6.00 diopters.
Summary
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
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Get my Genome Test9 genes linked to Moderate myopia
Changes in these genes cause rare conditions in which Moderate myopia 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 |
|---|---|---|
| BBS2Bardet-Biedl syndrome 2 | Always | In 1 condition |
| PDE6Bphosphodiesterase 6B | Always | In 1 condition |
| UBAP1Lubiquitin associated protein 1 like | Always | In 1 condition |
| ASPHaspartate beta-hydroxylase | Often (30–79%) | In 1 condition |
| COL9A3collagen type IX alpha 3 chain | Often (30–79%) | In 1 condition |
| H4C3H4 clustered histone 3 | Often (30–79%) | In 1 condition |
| TBC1D32TBC1 domain family member 32 | Often (30–79%) | In 1 condition |
| FLNAfilamin A | Sometimes (5–29%) | In 1 condition |
| H4C5H4 clustered histone 5 | Sometimes (5–29%) | 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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