Trait
Generalized edema
Generalized abnormal accumulation of fluid beneath the skin, or in one or more cavities of the body.
Summary
- Also called
- Generalised oedema, Generalised tissue oedema, Generalized tissue edema
- Body system
- Laboratory abnormality
Reference genomeGRCh38hg38
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Get my Genome Test18 genes linked to Generalized edema
Changes in these genes cause rare conditions in which Generalized 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 |
|---|---|---|
| MOGSmannosyl-oligosaccharide glucosidase | Always | In 2 conditions |
| NOS1APnitric oxide synthase 1 adaptor protein | Always | In 1 condition |
| ARHGDIARho GDP dissociation inhibitor alpha | Often (30–79%) | In 1 condition |
| CD46CD46 molecule | Often (30–79%) | In 1 condition |
| CFHcomplement factor H | Often (30–79%) | In 1 condition |
| CFIcomplement factor I | Often (30–79%) | In 1 condition |
| HELLPARHELLP associated long non-coding RNA | Often (30–79%) | In 1 condition |
| PHGDHphosphoglycerate dehydrogenase | Often (30–79%) | In 1 condition |
| TMEM260transmembrane protein 260 | Often (30–79%) | In 1 condition |
| FSHRfollicle stimulating hormone receptor | Sometimes (5–29%) | In 1 condition |
| IFT56intraflagellar transport 56 | Sometimes (5–29%) | In 1 condition |
| CALCRLcalcitonin receptor like receptor | Not recorded | In 1 condition |
| CD55CD55 molecule (Cromer blood group) | Not recorded | In 1 condition |
| DOK7docking protein 7 | Not recorded | In 1 condition |
| MYLKmyosin light chain kinase | Not recorded | In 1 condition |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Not recorded | In 1 condition |
| PRF1perforin 1 | Not recorded | In 1 condition |
| UBR1ubiquitin protein ligase E3 component n-recognin 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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