Trait
Fullness of upper eyelid
Clinical name: Upper eyelid edema
Edema in the region of the upper eyelid.
Summary
- Also called
- Puffiness of upper eyelid, Swelling of upper eyelid, Cellulitis of upper eyelid, Upper eyelid oedema
Reference genomeGRCh38hg38
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Get my Genome Test6 genes linked to Fullness of upper eyelid
Changes in these genes cause rare conditions in which Fullness of upper eyelid 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 |
|---|---|---|
| RIN2Ras and Rab interactor 2 | Very often (80–99%) | In 1 condition |
| MED12Lmediator complex subunit 12L | Often (30–79%) | In 1 condition |
| DHX30DExH-box helicase 30 | Sometimes (5–29%) | In 1 condition |
| KAT6Alysine acetyltransferase 6A | Sometimes (5–29%) | In 1 condition |
| SLC29A3solute carrier family 29 member 3 | Sometimes (5–29%) | In 1 condition |
| FRMD4AFERM domain containing 4A | 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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