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Trait
Excess fluid in lungs
Clinical name: Pulmonary edema
Fluid accumulation in the lungs.
Summary
- Also called
- Wet lung, Lung edema, Lung oedema
Excess fluid in lungsHP:0100598
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Get my Genome Test30 genes linked to Excess fluid in lungs
Changes in these genes cause rare conditions in which Excess fluid in lungs 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 |
|---|---|---|
| ARID2AT-rich interaction domain 2 | Always | In 1 condition |
| DNM1Ldynamin 1L | Always | In 1 condition |
| ABCA3ATP binding cassette subfamily A member 3 | Often (30–79%) | In 1 condition |
| CORINcorin, serine peptidase | Often (30–79%) | In 1 condition |
| FLT1fms related receptor tyrosine kinase 1 | Often (30–79%) | In 1 condition |
| MYBPC3myosin binding protein C3 | Often (30–79%) | In 1 condition |
| RRAGDRas related GTP binding D | Often (30–79%) | In 1 condition |
| SFTPBsurfactant protein B | Often (30–79%) | In 1 condition |
| SFTPCsurfactant protein C | Often (30–79%) | In 1 condition |
| STOX1storkhead box 1 | Often (30–79%) | In 1 condition |
| CD46CD46 molecule | Sometimes (5–29%) | In 1 condition |
| CFHcomplement factor H | Sometimes (5–29%) | In 1 condition |
| CFIcomplement factor I | Sometimes (5–29%) | In 1 condition |
| EIF2AK4eukaryotic translation initiation factor 2 alpha kinase 4 | Sometimes (5–29%) | In 1 condition |
| FLNCfilamin C | Sometimes (5–29%) | In 1 condition |
| FOCADfocadhesin | Sometimes (5–29%) | In 1 condition |
| FSHRfollicle stimulating hormone receptor | Sometimes (5–29%) | In 1 condition |
| HELLPARHELLP associated long non-coding RNA | Sometimes (5–29%) | In 1 condition |
| KIF20Akinesin family member 20A | Sometimes (5–29%) | In 1 condition |
| LRPPRCleucine rich pentatricopeptide repeat containing | Sometimes (5–29%) | In 1 condition |
| MOGSmannosyl-oligosaccharide glucosidase | Sometimes (5–29%) | In 1 condition |
| MYPNmyopalladin | Sometimes (5–29%) | In 1 condition |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Sometimes (5–29%) | In 1 condition |
| PLXND1plexin D1 | Sometimes (5–29%) | In 1 condition |
| PRKAG2protein kinase AMP-activated non-catalytic subunit gamma 2 | Sometimes (5–29%) | In 1 condition |
| TNNI3troponin I3, cardiac type | Sometimes (5–29%) | In 1 condition |
| TNNT2troponin T2, cardiac type | Sometimes (5–29%) | In 1 condition |
| TTRtransthyretin | Sometimes (5–29%) | In 1 condition |
| MT-CYBmitochondrially encoded cytochrome b | Rarely (1–4%) | In 1 condition |
| EPHB4EPH receptor B4 | 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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