Trait
Corneal perforation
A rupture of the cornea through which a portion of the iris protrudes.
Summary
- Also called
- Iridocele
- Body system
- Abnormality of the eye
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/corneal-perforation.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Corneal perforation, and the rest of your genome, with one test.
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Get my Genome Test14 genes linked to Corneal perforation
Changes in these genes cause rare conditions in which Corneal perforation 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 |
|---|---|---|
| PRDM5PR/SET domain 5 | Often (30–79%) | In 2 conditions |
| ZNF469zinc finger protein 469 | Often (30–79%) | In 1 condition |
| FOXE3forkhead box E3 | Sometimes (5–29%) | In 1 condition |
| ABCA12ATP binding cassette subfamily A member 12 | Rarely (1–4%) | In 1 condition |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Rarely (1–4%) | In 1 condition |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Rarely (1–4%) | In 1 condition |
| ASPRV1aspartic peptidase retroviral like 1 | Rarely (1–4%) | In 1 condition |
| CYP4F22cytochrome P450 family 4 subfamily F member 22 | Rarely (1–4%) | In 1 condition |
| LIPNlipase family member N | Rarely (1–4%) | In 1 condition |
| NIPAL4NIPA like domain containing 4 | Rarely (1–4%) | In 1 condition |
| SDR9C7short chain dehydrogenase/reductase family 9C member 7 | Rarely (1–4%) | In 1 condition |
| SULT2B1sulfotransferase family 2B member 1 | Rarely (1–4%) | In 1 condition |
| TGM1transglutaminase 1 | Rarely (1–4%) | In 1 condition |
| FGFR2fibroblast growth factor receptor 2 | 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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