Kenmerk
Sore in the lining of gastrointestinal tract
Klinische naam: Peptic ulcer
The term peptic ulcer refers to acid peptic injury of the digestive tract, resulting in mucosal break reaching the submucosa. Peptic ulcers are usually located in the stomach or proximal duodenum, but they can also be found in the esophagus or Meckel's diverticulum. Infection with Helicobacter pylori and the use of non steroidal antiinflammatory drugs (NSAIDs) or aspirin are the main risk factors of both gastric and duodenal peptic ulcers.
Samenvatting
- Lichaamssysteem
- Abnormality of the digestive system
Deze pagina als gegevens
Voeg .json toe aan het adres van de pagina, of vraag application/json aan, om haar als JSON te lezen.
library(jsonlite)
url <- "https://dantelabs.com/traits/peptic-ulcer.json"
page <- fromJSON(url)
page$trait$nameLees de genen die aan Sore in the lining of gastrointestinal tract gekoppeld zijn, en de rest van uw genoom, met één test.
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Mijn Genome Test bestellen12 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Inherited Parathyroid & Calcium-Sensing DisordersReads 3 of these genesAP2S1CDC73GNA11About this report →
- Malignant Endocrine NeoplasmReads 3 of these genesCDKN1BMEN1CDC73About this report →
- Wolfram Syndrome & WFS1 SpectrumReads 1 of these genesCISD2About this report →
- Thyroid CancerReads 3 of these genesMEN1CDC73GNA11About this report →
Show 8 more reports
- Hereditary Gastrointestinal Stromal TumourReads 1 of these genesKITAbout this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Other Inborn Errors of ImmunityReads 2 of these genesNCF1TET2About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesDNAJC30About this report →
- Intellectual DisabilityReads 1 of these genesASXL1About this report →
Lees de genen die aan Sore in the lining of gastrointestinal tract gekoppeld zijn, en de rest van uw genoom, met één test.
Vanaf $ 449Gratis verzending · Resultaten binnen 6–8 weken
Mijn Genome Test bestellen31 genen gekoppeld aan Sore in the lining of gastrointestinal tract
Veranderingen in deze genen veroorzaken zeldzame aandoeningen waarbij Sore in the lining of gastrointestinal tract voorkomt. De meeste mensen met dit kenmerk hebben geen van die aandoeningen, en een gen op deze lijst zegt niets over het eigen genoom van iemand.
| Gen | Hoe vaak het voorkomt | Aandoeningen |
|---|---|---|
| CDKN1Bcyclin dependent kinase inhibitor 1B | Vaak (30–79%) | In 2 aandoeningen |
| CDKN2Bcyclin dependent kinase inhibitor 2B | Vaak (30–79%) | In 1 aandoening |
| CISD2CDGSH iron sulfur domain 2 | Vaak (30–79%) | In 1 aandoening |
| MEN1menin 1 | Vaak (30–79%) | In 2 aandoeningen |
| AP2S1adaptor related protein complex 2 subunit sigma 1 | Soms (5–29%) | In 1 aandoening |
| ASXL1ASXL transcriptional regulator 1 | Soms (5–29%) | In 1 aandoening |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Soms (5–29%) | In 1 aandoening |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Soms (5–29%) | In 1 aandoening |
| CDC73cell division cycle 73 | Soms (5–29%) | In 2 aandoeningen |
| CLIP2CAP-Gly domain containing linker protein 2 | Soms (5–29%) | In 1 aandoening |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Soms (5–29%) | In 1 aandoening |
| EIF4Heukaryotic translation initiation factor 4H | Soms (5–29%) | In 1 aandoening |
| ELNelastin | Soms (5–29%) | In 1 aandoening |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Soms (5–29%) | In 1 aandoening |
| GNA11G protein subunit alpha 11 | Soms (5–29%) | In 1 aandoening |
| GTF2Igeneral transcription factor IIi | Soms (5–29%) | In 1 aandoening |
| GTF2IRD1GTF2I repeat domain containing 1 | Soms (5–29%) | In 1 aandoening |
| GTF2IRD2GTF2I repeat domain containing 2 | Soms (5–29%) | In 1 aandoening |
| HPGD15-hydroxyprostaglandin dehydrogenase | Soms (5–29%) | In 1 aandoening |
| KITKIT proto-oncogene, receptor tyrosine kinase | Soms (5–29%) | In 1 aandoening |
| LIMK1LIM domain kinase 1 | Soms (5–29%) | In 1 aandoening |
| METTL27methyltransferase like 27 | Soms (5–29%) | In 1 aandoening |
| NCF1neutrophil cytosolic factor 1 | Soms (5–29%) | In 1 aandoening |
| RFC2replication factor C subunit 2 | Soms (5–29%) | In 1 aandoening |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Soms (5–29%) | In 1 aandoening |
| SRSF2serine and arginine rich splicing factor 2 | Soms (5–29%) | In 1 aandoening |
| STX1Asyntaxin 1A | Soms (5–29%) | In 1 aandoening |
| TBL2transducin beta like 2 | Soms (5–29%) | In 1 aandoening |
| TET2tet methylcytosine dioxygenase 2 | Soms (5–29%) | In 1 aandoening |
| TMEM270transmembrane protein 270 | Soms (5–29%) | In 1 aandoening |
| VPS37DVPS37D subunit of ESCRT-I | Soms (5–29%) | In 1 aandoening |
Hoe vaak dit voorkomt bij mensen met een van de aandoeningen van het gen, de hoogste frequentie binnen die aandoeningen, zoals de Human Phenotype Ontology dit vastlegt. Deze pagina's beschrijven kenmerken en het onderzoek erachter; het zijn geen diagnose, en over symptomen kunt u het best een arts of genetisch adviseur raadplegen.
Smallere kenmerken
Bredere kenmerken
Waar dit vandaan komt
- De Human Phenotype Ontology, release 2026-09-01: het kenmerk, de namen, de definitie en de genen die ermee verbonden zijn. Meer informatie vindt u op hpo.jax.org.
- Gegevensrelease 2026.10.19-9814e911.
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