Trait
Abdominal symptom
A subjective manifestation of disease localized to the abdomen.
Summary
- Body system
- Abnormality of the digestive system
Reference genomeGRCh38hg38
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Get my Genome Test6 genes linked to Abdominal symptom
Changes in these genes cause rare conditions in which Abdominal symptom 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 |
|---|---|---|
| PRNPprion protein (Kanno blood group) | Very often (80–99%) | In 1 condition |
| CDC73cell division cycle 73 | Sometimes (5–29%) | In 1 condition |
| GCM2GCM transcription factor 2 | Sometimes (5–29%) | In 1 condition |
| GNASGNAS complex locus | Sometimes (5–29%) | In 3 conditions |
| MEN1menin 1 | Sometimes (5–29%) | In 1 condition |
| STX16syntaxin 16 | Sometimes (5–29%) | 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.
Narrower traits
- Feeding difficulties890 genes
- Constipation415 genes
- Abdominal pain327 genes
- Diarrhea316 genes
- Nausea and vomiting153 genes
- Abdominal bloating135 genes
- Anorexia132 genes
- Poor appetite51 genes
- Malnutrition43 genes
- Feeling full quickly when eating8 genes
- Protein avoidance6 genes
- Abnormal bowel sounds5 genes
- Bowel irritability2 genes
- Flatulence2 genes
- Aerophagia1 gene
- Meteorism1 gene
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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