Trait
Leukocoria
An abnormal white reflection from the pupil rather than the usual black reflection.
Summary
- Also called
- Leukokoria, White pupillary reflex
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
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Get my Genome Test10 genes linked to Leukocoria
Changes in these genes cause rare conditions in which Leukocoria 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 |
|---|---|---|
| ATOH7atonal bHLH transcription factor 7 | Always | In 2 conditions |
| FZD4frizzled class receptor 4 | Very often (80–99%) | In 1 condition |
| NDPnorrin cystine knot growth factor NDP | Very often (80–99%) | In 2 conditions |
| ARL6IP6ARF like GTPase 6 interacting protein 6 | Often (30–79%) | In 1 condition |
| GNA11G protein subunit alpha 11 | Often (30–79%) | In 1 condition |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Often (30–79%) | In 1 condition |
| LRP5LDL receptor related protein 5 | Often (30–79%) | In 1 condition |
| SPOUT1SPOUT domain containing methyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| RB1RB transcriptional corepressor 1 | Not recorded | In 1 condition |
| TINF2TERF1 interacting nuclear factor 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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