Trait
Stomach hernia
Clinical name: Hiatus hernia
The presence of a hernia in which the upper part of the stomach, i.e., mainly the gastric cardia protrudes through the diaphragmatic esophageal hiatus.
Summary
- Also called
- Hiatal hernia
Reference genomeGRCh38hg38
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Get my Genome Test39 genes linked to Stomach hernia
Changes in these genes cause rare conditions in which Stomach hernia 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 |
|---|---|---|
| GLRBglycine receptor beta | Always | In 2 conditions |
| ADAMTS2ADAM metallopeptidase with thrombospondin type 1 motif 2 | Very often (80–99%) | In 1 condition |
| ADAMTSL2ADAMTS like 2 | Very often (80–99%) | In 1 condition |
| ATAD1ATPase family AAA domain containing 1 | Very often (80–99%) | In 1 condition |
| GLRA1glycine receptor alpha 1 | Very often (80–99%) | In 1 condition |
| GPHNgephyrin | Very often (80–99%) | In 1 condition |
| SLC6A5solute carrier family 6 member 5 | Very often (80–99%) | In 2 conditions |
| TCF4transcription factor 4 | Very often (80–99%) | In 1 condition |
| ATP7AATPase copper transporting alpha | Often (30–79%) | In 2 conditions |
| CAMTA1calmodulin binding transcription activator 1 | Often (30–79%) | In 1 condition |
| GON7GON7 subunit of KEOPS complex | Often (30–79%) | In 1 condition |
| LAGE3L antigen family member 3 | Often (30–79%) | In 1 condition |
| MYH11myosin heavy chain 11 | Often (30–79%) | In 1 condition |
| NUP107nucleoporin 107 | Often (30–79%) | In 1 condition |
| NUP133nucleoporin 133 | Often (30–79%) | In 1 condition |
| OSGEPO-sialoglycoprotein endopeptidase | Often (30–79%) | In 2 conditions |
| TP53RKTP53 regulating kinase | Often (30–79%) | In 1 condition |
| TPRKBTP53RK binding protein | Often (30–79%) | In 1 condition |
| WDR4WDR4 tRNA N7-guanosine methyltransferase non-catalytic subunit | Often (30–79%) | In 1 condition |
| WDR73WD repeat domain 73 | Often (30–79%) | In 2 conditions |
| YRDCyrdC N6-threonylcarbamoyltransferase domain containing | Often (30–79%) | In 1 condition |
| C1Rcomplement C1r | Sometimes (5–29%) | In 1 condition |
| COL1A1collagen type I alpha 1 chain | Sometimes (5–29%) | In 1 condition |
| COL5A1collagen type V alpha 1 chain | Sometimes (5–29%) | In 2 conditions |
| COL5A2collagen type V alpha 2 chain | Sometimes (5–29%) | In 1 condition |
| EXT2exostosin glycosyltransferase 2 | Sometimes (5–29%) | In 1 condition |
| FBXO22F-box protein 22 | Sometimes (5–29%) | In 1 condition |
| GLIS3GLIS family zinc finger 3 | Sometimes (5–29%) | In 1 condition |
| MED12mediator complex subunit 12 | Sometimes (5–29%) | In 1 condition |
| SLC2A10solute carrier family 2 member 10 | Sometimes (5–29%) | In 2 conditions |
| TGFB3transforming growth factor beta 3 | Sometimes (5–29%) | In 1 condition |
| ZBTB7Azinc finger and BTB domain containing 7A | Sometimes (5–29%) | In 1 condition |
| ZNF699zinc finger protein 699 | Sometimes (5–29%) | In 1 condition |
| TRAF7TNF receptor associated factor 7 | Rarely (1–4%) | In 1 condition |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Not recorded | In 1 condition |
| CHST14carbohydrate sulfotransferase 14 | Not recorded | In 1 condition |
| NIPBLNIPBL cohesin loading factor | Not recorded | In 1 condition |
| PORCNporcupine O-acyltransferase | Not recorded | In 1 condition |
| TNXBtenascin XB | 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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