Trait
Duodenitis
Inflammation of the lining of the upper small intestine (duodenum).
Summary
- Also called
- Duodenal inflammation
- Body system
- Abnormality of the digestive system
Reference genomeGRCh38hg38
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Get my Genome Test6 genes linked to Duodenitis
Changes in these genes cause rare conditions in which Duodenitis 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 |
|---|---|---|
| ADAM17ADAM metallopeptidase domain 17 | Always | In 1 condition |
| FLT3LGfms related receptor tyrosine kinase 3 ligand | Always | In 1 condition |
| IRF4interferon regulatory factor 4 | Always | In 1 condition |
| PTCRApre T cell antigen receptor alpha | Always | In 1 condition |
| IPO8importin 8 | Sometimes (5–29%) | In 1 condition |
| CARD8caspase recruitment domain family member 8 | 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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