Požymis
Descending aortic dissection
A separation of the layers within the wall of the descending aorta. Tears in the intimal layer result in the propagation of dissection (proximally or distally) secondary to blood entering the intima-media space.
Santrauka
- Taip pat vadinama
- Type B aortic dissection
- Kūno sistema
- Abnormality of the cardiovascular system
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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/descending-aortic-dissection.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Descending aortic dissection, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test17 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.
- Aortic AneurysmReads 12 of these genesACTA2FBN1FOXE3LOXMFAP5MYH11About this report →
- Loeys-Dietz SyndromeReads 6 of these genesSMAD2SMAD3TGFB2TGFB3TGFBR1TGFBR2About this report →
- Marfan Like SyndromesReads 7 of these genesFBN1SMAD2SMAD3TGFB2TGFB3TGFBR1About this report →
- Ferguson-Smith Disease (Multiple Self-Healing Squamous Epithelioma)Reads 1 of these genesTGFBR1About this report →
Show 13 more reports
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 2 of these genesMYH11MYLKAbout this report →
- Cutis LaxaReads 3 of these genesEFEMP2ELNEMILIN1About this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- Moyamoya DiseaseReads 1 of these genesACTA2About this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesFOXE3About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Ehlers-Danlos SyndromeReads 1 of these genesCOL3A1About this report →
- Spinal Muscular AtrophyReads 1 of these genesEMILIN1About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesEMILIN1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesEMILIN1About this report →
- Intellectual DisabilityReads 1 of these genesSMAD4About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesEMILIN1About this report →
Vienu tyrimu sužinokite genus, susijusius su Descending aortic dissection, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test22 genų susiję su Descending aortic dissection
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Descending aortic dissection. 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 |
|---|---|---|
| ACTA2actin alpha 2, smooth muscle | Dažnai (30–79%) | 2 ligose |
| COL3A1collagen type III alpha 1 chain | Dažnai (30–79%) | 1 ligoje |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | Dažnai (30–79%) | 1 ligoje |
| ELNelastin | Dažnai (30–79%) | 1 ligoje |
| EMILIN1elastin microfibril interfacer 1 | Dažnai (30–79%) | 1 ligoje |
| FBN1fibrillin 1 | Dažnai (30–79%) | 1 ligoje |
| FOXE3forkhead box E3 | Dažnai (30–79%) | 2 ligose |
| HEY2hes related family bHLH transcription factor with YRPW motif 2 | Dažnai (30–79%) | 1 ligoje |
| LOXlysyl oxidase | Dažnai (30–79%) | 1 ligoje |
| MAT2Amethionine adenosyltransferase 2A | Dažnai (30–79%) | 1 ligoje |
| MFAP5microfibril associated protein 5 | Dažnai (30–79%) | 1 ligoje |
| MYH11myosin heavy chain 11 | Dažnai (30–79%) | 3 ligose |
| MYLKmyosin light chain kinase | Dažnai (30–79%) | 2 ligose |
| PRKG1protein kinase cGMP-dependent 1 | Dažnai (30–79%) | 2 ligose |
| SMAD2SMAD family member 2 | Dažnai (30–79%) | 1 ligoje |
| SMAD3SMAD family member 3 | Dažnai (30–79%) | 2 ligose |
| SMAD4SMAD family member 4 | Dažnai (30–79%) | 1 ligoje |
| TGFB2transforming growth factor beta 2 | Dažnai (30–79%) | 1 ligoje |
| TGFB3transforming growth factor beta 3 | Dažnai (30–79%) | 1 ligoje |
| TGFBR1transforming growth factor beta receptor 1 | Dažnai (30–79%) | 1 ligoje |
| TGFBR2transforming growth factor beta receptor 2 | Dažnai (30–79%) | 2 ligose |
| THSD4thrombospondin type 1 domain containing 4 | Dažnai (30–79%) | 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 2026.10.19-9814e911.
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