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Trait
Periorbital edema
Edema affecting the region situated around the orbit of the eye.
Summary
- Also called
- Periorbital cellulitis, Periorbital oedema
Periorbital edemaHP:0100539
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Read the genes linked to Periorbital edema, and the rest of your genome, with one test.
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Get my Genome Test70 genes linked to Periorbital edema
Changes in these genes cause rare conditions in which Periorbital edema 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 |
|---|---|---|
| LYNLYN proto-oncogene, Src family tyrosine kinase | Always | In 1 condition |
| PLD4phospholipase D family member 4 | Always | In 1 condition |
| SERPING1serpin family G member 1 | Always | In 1 condition |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Very often (80–99%) | In 1 condition |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Very often (80–99%) | In 1 condition |
| CLIP2CAP-Gly domain containing linker protein 2 | Very often (80–99%) | In 1 condition |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Very often (80–99%) | In 1 condition |
| EIF4Heukaryotic translation initiation factor 4H | Very often (80–99%) | In 1 condition |
| ELNelastin | Very often (80–99%) | In 1 condition |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Very often (80–99%) | In 1 condition |
| GTF2Igeneral transcription factor IIi | Very often (80–99%) | In 1 condition |
| GTF2IRD1GTF2I repeat domain containing 1 | Very often (80–99%) | In 1 condition |
| GTF2IRD2GTF2I repeat domain containing 2 | Very often (80–99%) | In 1 condition |
| LIMK1LIM domain kinase 1 | Very often (80–99%) | In 1 condition |
| METTL27methyltransferase like 27 | Very often (80–99%) | In 1 condition |
| NCF1neutrophil cytosolic factor 1 | Very often (80–99%) | In 1 condition |
| RFC2replication factor C subunit 2 | Very often (80–99%) | In 1 condition |
| STX1Asyntaxin 1A | Very often (80–99%) | In 1 condition |
| TBL2transducin beta like 2 | Very often (80–99%) | In 1 condition |
| TMEM270transmembrane protein 270 | Very often (80–99%) | In 1 condition |
| VPS37DVPS37D subunit of ESCRT-I | Very often (80–99%) | In 1 condition |
| ACTN4actinin alpha 4 | Often (30–79%) | In 1 condition |
| ANKFY1ankyrin repeat and FYVE domain containing 1 | Often (30–79%) | In 1 condition |
| ANLNanillin, actin binding protein | Often (30–79%) | In 1 condition |
| APOL1apolipoprotein L1 | Often (30–79%) | In 1 condition |
| ARHGAP24Rho GTPase activating protein 24 | Often (30–79%) | In 1 condition |
| ARHGDIARho GDP dissociation inhibitor alpha | Often (30–79%) | In 1 condition |
| AVILadvillin | Often (30–79%) | In 1 condition |
| CD2APCD2 associated protein | Often (30–79%) | In 1 condition |
| COL4A3collagen type IV alpha 3 chain | Often (30–79%) | In 1 condition |
| COQ8Bcoenzyme Q8B | Often (30–79%) | In 1 condition |
| CRB2crumbs cell polarity complex component 2 | Often (30–79%) | In 1 condition |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Often (30–79%) | In 1 condition |
| DAAM2dishevelled associated activator of morphogenesis 2 | Often (30–79%) | In 1 condition |
| EMP2epithelial membrane protein 2 | Often (30–79%) | In 1 condition |
| GAPVD1GTPase activating protein and VPS9 domains 1 | Often (30–79%) | In 1 condition |
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | Often (30–79%) | In 1 condition |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | Often (30–79%) | In 1 condition |
| INF2inverted formin 2 | Often (30–79%) | In 1 condition |
| KANK2KN motif and ankyrin repeat domains 2 | Often (30–79%) | In 1 condition |
Show 30 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| LAMA5laminin subunit alpha 5 | Often (30–79%) | In 1 condition |
| MAGI2membrane associated guanylate kinase, WW and PDZ domain containing 2 | Often (30–79%) | In 1 condition |
| MYO1Emyosin IE | Often (30–79%) | In 1 condition |
| NPHS1NPHS1 adhesion molecule, nephrin | Often (30–79%) | In 1 condition |
| NPHS2NPHS2 stomatin family member, podocin | Often (30–79%) | In 1 condition |
| NUP107nucleoporin 107 | Often (30–79%) | In 1 condition |
| NUP133nucleoporin 133 | Often (30–79%) | In 1 condition |
| NUP160nucleoporin 160 | Often (30–79%) | In 1 condition |
| NUP205nucleoporin 205 | Often (30–79%) | In 1 condition |
| NUP37nucleoporin 37 | Often (30–79%) | In 1 condition |
| NUP85nucleoporin 85 | Often (30–79%) | In 1 condition |
| NUP93nucleoporin 93 | Often (30–79%) | In 1 condition |
| PAX2paired box 2 | Often (30–79%) | In 1 condition |
| PLCE1phospholipase C epsilon 1 | Often (30–79%) | In 1 condition |
| PRTN3proteinase 3 | Often (30–79%) | In 1 condition |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Often (30–79%) | In 1 condition |
| PTPROprotein tyrosine phosphatase receptor type O | Often (30–79%) | In 1 condition |
| TBC1D8BTBC1 domain family member 8B | Often (30–79%) | In 1 condition |
| TRPC6transient receptor potential cation channel subfamily C member 6 | Often (30–79%) | In 1 condition |
| WT1WT1 transcription factor | Often (30–79%) | In 1 condition |
| EPHB4EPH receptor B4 | Sometimes (5–29%) | In 1 condition |
| IGSF3immunoglobulin superfamily member 3 | Sometimes (5–29%) | In 1 condition |
| LTBP4latent transforming growth factor beta binding protein 4 | Sometimes (5–29%) | In 1 condition |
| MYD88MYD88 innate immune signal transduction adaptor | Sometimes (5–29%) | In 1 condition |
| TNFRSF1ATNF receptor superfamily member 1A | Sometimes (5–29%) | In 2 conditions |
| CCBE1collagen and calcium binding EGF domains 1 | Not recorded | In 1 condition |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Not recorded | In 1 condition |
| POMPproteasome maturation protein | Not recorded | In 1 condition |
| PSMB4proteasome 20S subunit beta 4 | Not recorded | In 1 condition |
| SUMF1sulfatase modifying factor 1 | 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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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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