Trait
Intestinal obstruction
Blockage or impairment of the normal flow of the contents of the intestine towards the anal canal.
Summary
- Also called
- Bowel obstruction, Intestinal blockage
- Body system
- Abnormality of the digestive system
Reference genomeGRCh38hg38
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Get my Genome Test50 genes linked to Intestinal obstruction
Changes in these genes cause rare conditions in which Intestinal obstruction 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 |
|---|---|---|
| TTC7Atetratricopeptide repeat domain 7A | Always | In 1 condition |
| ABCD1ATP binding cassette subfamily D member 1 | Very often (80–99%) | In 1 condition |
| ATP7AATPase copper transporting alpha | Very often (80–99%) | In 1 condition |
| ECE1endothelin converting enzyme 1 | Very often (80–99%) | In 1 condition |
| EDN3endothelin 3 | Very often (80–99%) | In 2 conditions |
| EDNRBendothelin receptor type B | Very often (80–99%) | In 2 conditions |
| ERBB2erb-b2 receptor tyrosine kinase 2 | Very often (80–99%) | In 1 condition |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Very often (80–99%) | In 1 condition |
| GDNFglial cell derived neurotrophic factor | Very often (80–99%) | In 1 condition |
| MITFmelanocyte inducing transcription factor | Very often (80–99%) | In 1 condition |
| NRTNneurturin | Very often (80–99%) | In 1 condition |
| RETret proto-oncogene | Very often (80–99%) | In 1 condition |
| SEMA3Csemaphorin 3C | Very often (80–99%) | In 1 condition |
| SEMA3Dsemaphorin 3D | Very often (80–99%) | In 1 condition |
| SMOsmoothened, frizzled class receptor | Very often (80–99%) | In 1 condition |
| SOX10SRY-box transcription factor 10 | Very often (80–99%) | In 1 condition |
| SREBF1sterol regulatory element binding transcription factor 1 | Very often (80–99%) | In 1 condition |
| KITKIT proto-oncogene, receptor tyrosine kinase | Often (30–79%) | In 2 conditions |
| PDGFRAplatelet derived growth factor receptor alpha | Often (30–79%) | In 1 condition |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Often (30–79%) | In 2 conditions |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Often (30–79%) | In 3 conditions |
| SDHCsuccinate dehydrogenase complex subunit C | Often (30–79%) | In 3 conditions |
| SDHDsuccinate dehydrogenase complex subunit D | Often (30–79%) | In 1 condition |
| TNFRSF1ATNF receptor superfamily member 1A | Often (30–79%) | In 1 condition |
| APCAPC regulator of Wnt signaling pathway | Sometimes (5–29%) | In 1 condition |
| CALRcalreticulin | Sometimes (5–29%) | In 1 condition |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Sometimes (5–29%) | In 1 condition |
| CTNNB1catenin beta 1 | Sometimes (5–29%) | In 1 condition |
| EFEMP1EGF-like fibulin extracellular matrix protein 1 | Sometimes (5–29%) | In 1 condition |
| F5coagulation factor V | Sometimes (5–29%) | In 1 condition |
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | Sometimes (5–29%) | In 1 condition |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | Sometimes (5–29%) | In 1 condition |
| JAK2Janus kinase 2 | Sometimes (5–29%) | In 1 condition |
| MEFVMEFV innate immunity regulator, pyrin | Sometimes (5–29%) | In 1 condition |
| MVKmevalonate kinase | Sometimes (5–29%) | In 1 condition |
| MYCMYC proto-oncogene, bHLH transcription factor | Sometimes (5–29%) | In 1 condition |
| MYH11myosin heavy chain 11 | Sometimes (5–29%) | In 1 condition |
| NOTCH3notch receptor 3 | Sometimes (5–29%) | In 1 condition |
| PDGFRBplatelet derived growth factor receptor beta | Sometimes (5–29%) | In 1 condition |
| PRTN3proteinase 3 | Sometimes (5–29%) | In 1 condition |
Show 10 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Sometimes (5–29%) | In 1 condition |
| STK11serine/threonine kinase 11 | Sometimes (5–29%) | In 1 condition |
| TBCEtubulin folding cofactor E | Sometimes (5–29%) | In 1 condition |
| EXT1exostosin glycosyltransferase 1 | Rarely (1–4%) | In 1 condition |
| EXT2exostosin glycosyltransferase 2 | Rarely (1–4%) | In 1 condition |
| CD55CD55 molecule (Cromer blood group) | Not recorded | In 1 condition |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Not recorded | In 1 condition |
| IL6interleukin 6 | Not recorded | In 1 condition |
| JAK3Janus kinase 3 | Not recorded | In 1 condition |
| NOD2nucleotide binding oligomerization domain containing 2 | 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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