Trait
Iridodonesis
Tremulousness of the iris on movement of the eye, occurring in subluxation of the lens.
Summary
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
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Get my Genome Test8 genes linked to Iridodonesis
Changes in these genes cause rare conditions in which Iridodonesis 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 |
|---|---|---|
| FBN1fibrillin 1 | Always | In 2 conditions |
| CPAMD8C3 and PZP like alpha-2-macroglobulin domain containing 8 | Often (30–79%) | In 1 condition |
| CYP1B1cytochrome P450 family 1 subfamily B member 1 | Sometimes (5–29%) | In 1 condition |
| LTBP2latent transforming growth factor beta binding protein 2 | Sometimes (5–29%) | In 2 conditions |
| MYOCmyocilin | Sometimes (5–29%) | In 1 condition |
| TEKTEK receptor tyrosine kinase | Sometimes (5–29%) | In 1 condition |
| ADAMTS17ADAM metallopeptidase with thrombospondin type 1 motif 17 | Not recorded | In 1 condition |
| CHRDL1chordin like 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.
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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