Trait
Falciform retinal fold
An area of the retina that is buckled so that a sector-shaped sheet of retina lies in front of the normal retina. This feature is of congenital onset.
Summary
- Also called
- Congenital retinal fold
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
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Get my Genome Test7 genes linked to Falciform retinal fold
Changes in these genes cause rare conditions in which Falciform retinal fold 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 |
|---|---|---|
| CTNNB1catenin beta 1 | Often (30–79%) | In 1 condition |
| FZD4frizzled class receptor 4 | Often (30–79%) | In 2 conditions |
| LRP5LDL receptor related protein 5 | Often (30–79%) | In 3 conditions |
| NDPnorrin cystine knot growth factor NDP | Often (30–79%) | In 2 conditions |
| TSPAN12tetraspanin 12 | Often (30–79%) | In 2 conditions |
| ZNF408zinc finger protein 408 | Often (30–79%) | In 2 conditions |
| LRP6LDL receptor related protein 6 | 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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