Trait
Abnormal peritoneum morphology
An abnormality of the peritoneum.
Summary
- Also called
- Abnormality of the peritoneum
- Body system
- Abnormality of the digestive system
Reference genomeGRCh38hg38
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Get my Genome Test9 genes linked to Abnormal peritoneum morphology
Changes in these genes cause rare conditions in which Abnormal peritoneum morphology 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 |
|---|---|---|
| EWSR1EWS RNA binding protein 1 | Very often (80–99%) | In 1 condition |
| WT1WT1 transcription factor | Very often (80–99%) | In 1 condition |
| BCL2BCL2 apoptosis regulator | Sometimes (5–29%) | In 1 condition |
| BCL6BCL6 transcription repressor | Sometimes (5–29%) | In 1 condition |
| ELP1elongator acetyltransferase complex subunit 1 | Sometimes (5–29%) | In 1 condition |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Sometimes (5–29%) | In 1 condition |
| IGHimmunoglobulin heavy locus | Sometimes (5–29%) | In 1 condition |
| NAB2NGFI-A binding protein 2 | Rarely (1–4%) | In 1 condition |
| STAT6signal transducer and activator of transcription 6 | Rarely (1–4%) | 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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