AtlasTrait
Fullness of eyelids
Clinical name: Palpebral edema
Edema in the region of the eyelids.
Summary
- Also called
- Puffy eyelids, Puffy lids, Swelling of eyelids, Edema of the eyelids, Eyelid edema, Eyelid oedema, Oedema of the eyelids, Palpebral oedema
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Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
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page <- fromJSON(url)
page$trait$nameRead the genes linked to Fullness of eyelids, and the rest of your genome, with one test.
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Get my Genome Test26 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Familial Isolated Pituitary Adenoma (FIPA / X-LAG)Reads 2 of these genesAIPGPR101About this report →
- GAPO SyndromeReads 1 of these genesANTXR1About this report →
- Scalp-Ear-Nipple SyndromeReads 1 of these genesKCTD1About this report →
- SPTBN1-Related Neurodevelopmental DisorderReads 1 of these genesSPTBN1About this report →
Show 22 more reports
- Activated PI3K-Delta Syndrome (APDS)Reads 1 of these genesPIK3CDAbout this report →
- Lissencephaly Spectrum DisordersReads 3 of these genesACTBACTG1PSPHAbout this report →
- Leukocyte Adhesion DeficiencyReads 1 of these genesSLC35C1About this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 2 of these genesPEX2PEX5About this report →
- Disorders of Glycine & Serine MetabolismReads 1 of these genesPSPHAbout this report →
- Inherited Neurodegenerative DisordersReads 5 of these genesSNX14ZNHIT3CAMTA1PEX2PEX5About this report →
- Cutis LaxaReads 1 of these genesRIN2About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesSOX18About this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTGFBIAbout this report →
- Other Inherited LeukodystrophiesReads 2 of these genesPEX2PEX5About this report →
- Inherited ThrombocytopeniasReads 1 of these genesACTBAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesCAMTA1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesACTBAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesSNX14About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesPEX2PEX5About this report →
- Lysosomal Storage DiseaseReads 1 of these genesGNPTABAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesACTG1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesSLC35C1About this report →
- Epilepsy (Full Panel)Reads 1 of these genesFOXG1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesPIK3CDAbout this report →
- Intellectual DisabilityReads 1 of these genesSHANK3About this report →
Read the genes linked to Fullness of eyelids, and the rest of your genome, with one test.
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Get my Genome Test29 genes linked to Fullness of eyelids
Changes in these genes cause rare conditions in which Fullness of eyelids 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 | Always | In 1 condition |
| ANTXR1ANTXR cell adhesion molecule 1 | Very often (80–99%) | In 1 condition |
| RBMXRNA binding motif protein X-linked | Very often (80–99%) | In 1 condition |
| AIPAHR interacting HSP90 co-chaperone | Often (30–79%) | In 1 condition |
| CACHD1cache domain containing 1 | Often (30–79%) | In 1 condition |
| FOXG1forkhead box G1 | Often (30–79%) | In 1 condition |
| FRMD4AFERM domain containing 4A | Often (30–79%) | In 1 condition |
| GPR101G protein-coupled receptor 101 | Often (30–79%) | In 1 condition |
| KCTD1potassium channel tetramerization domain containing 1 | Often (30–79%) | In 2 conditions |
| KNSTRNkinetochore localized astrin (SPAG5) binding protein | Often (30–79%) | In 1 condition |
| MED16mediator complex subunit 16 | Often (30–79%) | In 1 condition |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Often (30–79%) | In 1 condition |
| SHANK3SH3 and multiple ankyrin repeat domains 3 | Often (30–79%) | In 1 condition |
| SNX14sorting nexin 14 | Often (30–79%) | In 1 condition |
| SOX18SRY-box transcription factor 18 | Often (30–79%) | In 3 conditions |
| TGFBItransforming growth factor beta induced | Often (30–79%) | In 1 condition |
| XPNPEP2X-prolyl aminopeptidase 2 | Often (30–79%) | In 1 condition |
| ZNHIT3zinc finger HIT-type containing 3 | Often (30–79%) | In 1 condition |
| ACTBactin beta | Sometimes (5–29%) | In 1 condition |
| ACTG1actin gamma 1 | Sometimes (5–29%) | In 1 condition |
| CAMTA1calmodulin binding transcription activator 1 | Sometimes (5–29%) | In 2 conditions |
| KPTNkaptin, actin binding protein | Sometimes (5–29%) | In 1 condition |
| PSPHphosphoserine phosphatase | Sometimes (5–29%) | In 1 condition |
| SLC35C1solute carrier family 35 member C1 | Sometimes (5–29%) | In 1 condition |
| POU4F1POU class 4 homeobox 1 | Rarely (1–4%) | In 1 condition |
| SPTBN1spectrin beta, non-erythrocytic 1 | Rarely (1–4%) | In 1 condition |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Not recorded | In 1 condition |
| PEX2peroxisomal biogenesis factor 2 | Not recorded | In 1 condition |
| PEX5peroxisomal biogenesis factor 5 | 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.
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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 2026.10.19-9814e911.
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