Trait
Ileus
Acute obstruction of the intestines preventing passage of the contents of the intestines.
Summary
- Also called
- Gastrointestinal atony
- Body system
- Abnormality of the digestive system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test12 genes linked to Ileus
Changes in these genes cause rare conditions in which Ileus 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 |
|---|---|---|
| SOX10SRY-box transcription factor 10 | Very often (80–99%) | In 2 conditions |
| EWSR1EWS RNA binding protein 1 | Often (30–79%) | In 1 condition |
| SLC6A8solute carrier family 6 member 8 | Often (30–79%) | In 2 conditions |
| WT1WT1 transcription factor | Often (30–79%) | In 1 condition |
| HMBShydroxymethylbilane synthase | Sometimes (5–29%) | In 1 condition |
| KIF26Akinesin family member 26A | Sometimes (5–29%) | In 1 condition |
| PPOXprotoporphyrinogen oxidase | Sometimes (5–29%) | In 1 condition |
| CFTRCF transmembrane conductance regulator | Rarely (1–4%) | In 1 condition |
| FCGR2AFc gamma receptor IIa | Rarely (1–4%) | In 1 condition |
| FOXP3forkhead box P3 | Rarely (1–4%) | In 2 conditions |
| TGFB1transforming growth factor beta 1 | Rarely (1–4%) | In 1 condition |
| CAVIN1caveolae associated protein 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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