AtlasPožymis
Stomach hernia
Klinikinis pavadinimas: 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.
Santrauka
- Taip pat vadinama
- Hiatal hernia
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Ši puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/hiatus-hernia.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Stomach hernia, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test29 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.
- Ehlers-Danlos SyndromeReads 7 of these genesADAMTS2C1RCOL1A1COL5A1COL5A2CHST14About this report →
- Caffey DiseaseReads 1 of these genesCOL1A1About this report →
- Focal Dermal Hypoplasia (Goltz Syndrome)Reads 1 of these genesPORCNAbout this report →
- Hyperekplexia 3 (SLC6A5)Reads 1 of these genesSLC6A5About this report →
Show 25 more reports
- P5CS Deficiency (ALDH18A1-Related)Reads 1 of these genesALDH18A1About this report →
- Cutis LaxaReads 3 of these genesATP7ASLC2A10ALDH18A1About this report →
- Hereditary Multiple OsteochondromasReads 1 of these genesEXT2About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7AAbout this report →
- Molybdenum Cofactor & Isolated Sulfite Oxidase DeficiencyReads 1 of these genesGPHNAbout this report →
- Cornelia de Lange SyndromeReads 1 of these genesNIPBLAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesMYH11About this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFB3About this report →
- Nephrotic SyndromeReads 2 of these genesNUP107NUP133About this report →
- Marfan Like SyndromesReads 1 of these genesTGFB3About this report →
- Aortic AneurysmReads 1 of these genesMYH11About this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- Neonatal Diabetes MellitusReads 1 of these genesGLIS3About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesTRAF7About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesEXT2CHST14About this report →
- Spinal Muscular AtrophyReads 1 of these genesATP7AAbout this report →
- Diabetes MellitusReads 1 of these genesGLIS3About this report →
- Osteogenesis ImperfectaReads 1 of these genesCOL1A1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesCAMTA1About this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesATP7ACAMTA1ALDH18A1About this report →
- Female InfertilityReads 1 of these genesNUP107About this report →
- Intellectual DisabilityReads 2 of these genesTCF4MED12About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesALDH18A1About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesATP7AAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesATP7AAbout this report →
Vienu tyrimu sužinokite genus, susijusius su Stomach hernia, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test39 genų susiję su Stomach hernia
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Stomach hernia. Dauguma žmonių, turinčių šį požymį, neturi nė vienos iš tų ligų, o šiame sąraše esantis genas nieko nesako apie kieno nors paties genomą.
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| GLRBglycine receptor beta | Visada | 2 ligose |
| ADAMTS2ADAM metallopeptidase with thrombospondin type 1 motif 2 | Labai dažnai (80–99%) | 1 ligoje |
| ADAMTSL2ADAMTS like 2 | Labai dažnai (80–99%) | 1 ligoje |
| ATAD1ATPase family AAA domain containing 1 | Labai dažnai (80–99%) | 1 ligoje |
| GLRA1glycine receptor alpha 1 | Labai dažnai (80–99%) | 1 ligoje |
| GPHNgephyrin | Labai dažnai (80–99%) | 1 ligoje |
| SLC6A5solute carrier family 6 member 5 | Labai dažnai (80–99%) | 2 ligose |
| TCF4transcription factor 4 | Labai dažnai (80–99%) | 1 ligoje |
| ATP7AATPase copper transporting alpha | Dažnai (30–79%) | 2 ligose |
| CAMTA1calmodulin binding transcription activator 1 | Dažnai (30–79%) | 1 ligoje |
| GON7GON7 subunit of KEOPS complex | Dažnai (30–79%) | 1 ligoje |
| LAGE3L antigen family member 3 | Dažnai (30–79%) | 1 ligoje |
| MYH11myosin heavy chain 11 | Dažnai (30–79%) | 1 ligoje |
| NUP107nucleoporin 107 | Dažnai (30–79%) | 1 ligoje |
| NUP133nucleoporin 133 | Dažnai (30–79%) | 1 ligoje |
| OSGEPO-sialoglycoprotein endopeptidase | Dažnai (30–79%) | 2 ligose |
| TP53RKTP53 regulating kinase | Dažnai (30–79%) | 1 ligoje |
| TPRKBTP53RK binding protein | Dažnai (30–79%) | 1 ligoje |
| WDR4WDR4 tRNA N7-guanosine methyltransferase non-catalytic subunit | Dažnai (30–79%) | 1 ligoje |
| WDR73WD repeat domain 73 | Dažnai (30–79%) | 2 ligose |
| YRDCyrdC N6-threonylcarbamoyltransferase domain containing | Dažnai (30–79%) | 1 ligoje |
| C1Rcomplement C1r | Kartais (5–29%) | 1 ligoje |
| COL1A1collagen type I alpha 1 chain | Kartais (5–29%) | 1 ligoje |
| COL5A1collagen type V alpha 1 chain | Kartais (5–29%) | 2 ligose |
| COL5A2collagen type V alpha 2 chain | Kartais (5–29%) | 1 ligoje |
| EXT2exostosin glycosyltransferase 2 | Kartais (5–29%) | 1 ligoje |
| FBXO22F-box protein 22 | Kartais (5–29%) | 1 ligoje |
| GLIS3GLIS family zinc finger 3 | Kartais (5–29%) | 1 ligoje |
| MED12mediator complex subunit 12 | Kartais (5–29%) | 1 ligoje |
| SLC2A10solute carrier family 2 member 10 | Kartais (5–29%) | 2 ligose |
| TGFB3transforming growth factor beta 3 | Kartais (5–29%) | 1 ligoje |
| ZBTB7Azinc finger and BTB domain containing 7A | Kartais (5–29%) | 1 ligoje |
| ZNF699zinc finger protein 699 | Kartais (5–29%) | 1 ligoje |
| TRAF7TNF receptor associated factor 7 | Retai (1–4 %) | 1 ligoje |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Neužfiksuota | 1 ligoje |
| CHST14carbohydrate sulfotransferase 14 | Neužfiksuota | 1 ligoje |
| NIPBLNIPBL cohesin loading factor | Neužfiksuota | 1 ligoje |
| PORCNporcupine O-acyltransferase | Neužfiksuota | 1 ligoje |
| TNXBtenascin XB | Neužfiksuota | 1 ligoje |
Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.
Platesni požymiai
Iš kur tai žinoma
- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.21-311f020e.
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